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    02 July 2011, Volume 15 Issue 27 Previous Issue    Next Issue
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    Apoptotic mechanism of rat bone marrow mesenchymal stem cells induced by ethanol
    Ma Ai-guo, Zhao Jin-min, Su Wei, Li Xiao-feng, Fan Qie, Cui Xiang-rong
    2011, 15 (27):  4941-4945.  doi: 10.3969/j.issn.1673-8225.2011.27.001
    Abstract ( 99 )   PDF (1363KB) ( 416 )   Save

    BACKGROUND: Previous studies demonstrated that ethanol can induce apoptosis in bone marrow mesenchymal stem cells (BMSCs), and decrease the number of osteoplasts and osteoclasts. However, the effect and mechanism of ethanol on apoptosis in BMSCs remains unclear.
    OBJECTIVE: To investigate the effect of ethanol on apoptosis in BMSCs of rats and their mitochondrial function and to evaluate the pathway associated with the regulation of Bcl-2 and Caspase-3.
    METHODS: BMSCs were isolated from Sprague-Dawley rats were treated with ethanol at doses of 0, 100, 200, 300, 400, 500, 600, 700, 800, 900 mmol/L for 24 hours. cytotoxic drug experiment was performed with MTT assay. BMSCs were treated with ethanol at doses of 0, 100, 200, 300, 400, 500 mmol/L for 6, 12, 24 hours, AnnexinV/PI flow cytometry of double label method was performed to detect the apoptosis and mitochondrial membrane potential, BMSCs were treated with ethanol at doses of 0, 427 mmol/L for 24 hours, the levels of Bcl-2 and Caspase-3 mRNA expression were determined by RT-PCR method.
    RESULTS AND CONCLUSION: MTT assay results showed that 50% concentration of inhibition (IC50) of BMSCs of rats grew in ethanol was 427 mmol/L. The results of Annexin V/PI assay indicated that the apoptosis rates of BMSCs and mitochondrial membrane potential were higher than that of untreated (0 mmol/L) group when time and dose of ethanol was increased (P < 0.05). Compared with 0 mmol/L group, the level of Bcl-2mRNA expression was decreased in 427 mmol/L group after 24 hours, but the caspase-3 mRNA expression was increased significantly by treatment at 427 mmol/L (P < 0.05). These results suggest that ethanol can induce apoptosis in BMSCs of SD rat, and the occurrence of apoptosis may be related to the mitochondrial membrane potential damage, mitochondrial dysfunction, bcl-2 and Caspase-3 activation.

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    A large mass of mesenchymal stem cells isolated from tooth germs
    Yang Shao-guang, Xing Wen, Tian Kun, Liu Meng, Lu Shi-hong, Zhao Qin-jun, Ren Hong-ying, Chi Ying, Ma Feng-xia, Han Zhong-chao
    2011, 15 (27):  4946-4950.  doi: 10.3969/j.issn.1673-8225.2011.27.002
    Abstract ( 80 )   PDF (1269KB) ( 322 )   Save

    BACKGROUND: Mesenchymal stem cells have been isolated from dental tissues such as the dental pulp, the dental follicle and the periodontal ligament. It is unclear whether mesenchymal stem cells can be isolated directly from tooth germs, the tooth precursors. 
    OBJECTIVE: To isolate mesenchymal stem cells from tooth germs of aborted fetuses and to detect their biological characteristics.
    METHODS: The tooth germs were dug out entirely from fetal alveolar ridge aseptically. They were cut into small pieces and digested with collagenase Ⅱ and trypsin successively. After filtering the pieces out, the cells were washed and cultured. The expanded adherent cells were studied. Cell morphology, immunophenotype and multi-potential differentiation were analyzed.
    RESULTS AND CONCLUSION: After 3 passages, more than 107 homogenous, spindle-shaped adherent cells were obtained from one fetal tooth germ. These cells expressed the markers of CD105, CD73, CD90 and CD44, but they did not express CD34 and CD45. They could differentiate into osteoblasts and adipocytes in vitro, and chondrocytes in vivo. Mesenchymal stem cells can be isolated from fetal tooth germs by plastic adherence.

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    Differentiation of rabbit mesenchymal stem cells into chondrocytes in vitro
    Yu Meng, Yu Fang, Fu Sheng-liang
    2011, 15 (27):  4951-4954.  doi: 10.3969/j.issn.1673-8225.2011.27.003
    Abstract ( 88 )   PDF (1221KB) ( 581 )   Save

    BACKGROUND: Bone marrow mesenchymal stem cells (BMSCs) have a multi-differentiated potential to differentiate into bone, cartilage, tendon, adipose and so on.
    OBJECTIVE: To build a method of differentiation of rabbit BMSCs into chondrocytes in vitro and to determine the factors involved in the differentiation process.
    METHODS: BMSCs were isolated from young rabbit femur marrow, and then planted in plastic culture flask. After stimulated by basic fibroblast growth factor (bFGF), passage 3 cells were chosen to induce into cartilage differentiation in different concentrations of transforming growth factor-β1 (TGF-β1). Tow weeks later, the morphology of chondrocytes was detected by toludine blue, type Ⅱ collagen and aggrecan assay with RT-PCR.
    RESULTS AND CONCLUSION: bFGF could stimulate the proliferation of BMSCs. Induced BMSCs had typical appearance of chondrocytes, the expression of type Ⅱ collagen and aggrecan were positive. 10 μg/L TGF-β1 was the optimal concentration for cartilage differentiation.

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    Differentiation ability of bone marrow mesenchymal stem cells cultured by density gradient centrifugation in vitro
    Mu Xiao-hong, Zhao Zi-yi, Xu Lin, Wang Shuo-ren, Zhu Ling-qun, Liu Tong-hua
    2011, 15 (27):  4955-4958.  doi: 10.3969/j.issn.1673-8225.2011.27.004
    Abstract ( 108 )   PDF (1347KB) ( 477 )   Save

    BACKGROUND: Bone marrow mesenchymal stem cells (BMSCs) are capable of multiple directional differentiation, and are potential seed cells and target cells for gene therapy.
    OBJECTIVE: To observe in vitro cultured rabbit BMSCs, to understand its biological properties.
    METHODS: Density gradient centrifugation cultivation was utilized to culture rabbit BMSCs. The morphology and characteristics of cultured cells were observed. The surface markers CD29, CD34, CD44, CD45, CD166 and HLA-DR of cells were identified by flow cytometry, and its biological properties were identified.
    RESULTS AND CONCLUSION: High purity of rabbit BMSCs could be achieved by the density gradient centrifugation. The expressions of cell phenotypes were shown as follows respectively: CD29+, CD34-, CD44+, CD45-, CD166+, HLA-DR-. Under appropriate conditions, BMSCs were induced to differentiate into osteoblasts and cartilage cells.

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    In vitro differentiation of bone marrow mesenchymal stem cells induced by liver cirrhosis sera of rats into hepatocytes
    Fan Sha-sha, Shi Yong-zhong, Yuan You-hong, Cao You-de
    2011, 15 (27):  4959-4963.  doi: 10.3969/j.issn.1673-8225.2011.27.005
    Abstract ( 88 )   PDF (1320KB) ( 380 )   Save

    BACKGROUND: In recent years, the clinical use of bone marrow mesenchymal stem cells (BMSCs) transplantation for the treatment of liver fibrosis has achieved good effects, but the source of the liver is rare. The techniques for bone marrow stem cells differentiating into mature hepatocytes are still immature.
    OBJECTIVE: To discuss the possibility of the differentiation of BMSCs induced by liver cirrhosis sera of rats in vitro into hepatocytes.
    METHODS: Rat BMSCs were isolated, purified and identified; normal and liver cirrhosis sera of rats were prepared; the third passage BMSCs were divided into groups for culture: Group A: DMEM+10% fetal bovine serum (FBS); Group B: hepatocyte growth medium (HGM)+5% cirrhosis sera of rats; Group C: HGM+5% normal rat sera; Group D: HGM+5% liver cirrhosis sera of rats; Group E: HGM+5% liver cirrhosis sera of rats+25 μg hepatocyte growth factors (HGF). Cell morphology was observed and the cell growth curve was measured with MTT assay. The expressions of Alpha-fetoprotein and Cytokeratin18  were detected by reverse transcription polymerase chain reaction, and the albumin content in supernatant was determined by bromoeresol green method. Transforming growth factors β1 in supernatant was detected by ELISA.
    RESULTS AND CONCLUSION: Normal rat sera can obviously promote the proliferation of BMSCs; liver cirrhosis sera of rats are of certain effect on BMSCs proliferation and can effectively induce the differentiation of BMSCs into hepatocytes. The combined application with HGF can raise BMSCs differentiation.

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    Co-culture of bone marrow mesenchymal stem cells and nucleus pulposus cells in vitro 
    Xu Yuan, Yu Xing, Xu Lin
    2011, 15 (27):  4964-4968.  doi: 10.3969/j.issn.1673-8225.2011.27.006
    Abstract ( 73 )   PDF (669KB) ( 481 )   Save

    BACKGROUND: Using stem cell transplantation in the treatment of disc degeneration disease is still limited to the laboratory study.
    OBJECTIVE: To co-culture bone marrow mesenchymal stem cells (BMSCs) with the degenerative nucleus pulposus cells in vitro, and to explore whether BMSCs promote the expression of extracellular matrix of the nucleus pulposus cells and differentiate into nucleus pulposus-like cells in a directly contact microenvironment.
    METHODS: The 6th generation of naturally degenerated nucleus pulposus cells were isolated and co-cultured with the 4th generation of BMSCs through direct contact in vitro, according to different proportions (75:25, 50:50, 75:25). The pure nucleus pulposus cells (100:0) and pure BMSCs (0:100) acted as the positive and negative controls, respectively.
    RESULTS AND CONCLUSION: The results of reverse transcription-polymerase chain reaction of collagen II and aggrecan in the co-culture groups (75:25 and 50:50) showed brighter band than the positive control group (100:0), and there were significant differences of absorbance value. The results of immunohistochemical method of collagen II showed more expressions in the co-culture groups (75:25 and 50:50) than the positive control group (100:0). BMSCs turned into nucleus pulposus-like cells appearance and metachromatic granules increased in the co-culture group. Direct contact of MSCs and nucleus pulposus cell in vitro is essential for BMSCs reversing the nucleus pulposus cells degeneration and differentiating into nucleus pulposus-like cells.

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    Effects of sequential inductive systems with feeder cells from human aorta-gonad-mesonephros region, fetal liver and bone marrow on the differentiation of mouse embryonic stem cells into hematopoietic stem cells
    Cai Yun, Zhang Xu-chao, Chen Hui-qin, Huang Shao-liang
    2011, 15 (27):  4969-4974.  doi: 10.3969/j.issn.1673-8225.2011.27.007
    Abstract ( 146 )   PDF (736KB) ( 386 )   Save

    BACKGROUND: Previous studies have prepared human aorta-gonad-mesonephros (AGM) region stromal cell line and fetal liver stromal cell line, and found that AGM can promote directional differentiation of mouse embryonic stem cells (ESCs) into hemopoietic stem cells (HSCs).
    OBJECTIVE: To simulate the spatial and temporal hematopoietic microenvironment changes in embryonic development, investigate the supportive effects of sequential inductive systems with feeder cells from human AGM region and fetal liver and bone marrow on the differentiation of mouse ESCs into HSCs, and design more effective conditions for HSCs output.
    METHODS: E14 mouse ESCs were induced into embryoid body firstly. Then the cells from embryoid body were further co-cultured with human AGM region, fetal liver and bone marrow stromal cells in Transwell non-contact system in sequential orders. The induced embryoid body cells were divided into four groups according to different culture stages: embryoid body control group; embryoid body/AGM group; embryoid body/AGM+ fetal liver group; embryoid body /AGM+ fetal liver + bone marrow group. On day 6 of co-cultured, cells derived from embryoid body in all groups were collected for Sca-1+c-Kit+ cells analysis by flow cytometry, colony forming unit assay and observed.
    RESULTS AND CONCLUSION: ①Primitive hematopoietic cells were detected in embryoid body/AGM+fetal liver group and embryoid body/AGM+fetal liver+bone marrow group. ②Sca-1+c-Kit+ cell proportion of embryoid body/AGM group was much higher than pre-treated embryoid body cells (P < 0.05). ③Embryoid body/AGM group, embryoid body/AGM+fetal liver group and embryoid body/AGM+fetal liver+bone marrow group had more colony forming unit amount than embryoid body control group (P < 0.05). And the cells collected from embryoid body /AGM+ fetal liver group and embryoid body/AGM+ fetal liver + bone marrow group had better ability of forming multiple lineage hematopoietic colonies than that from embryoid body/AGM group. It suggested that microenvironment of AGM+ fetal liver or AGM+ fetal liver + bone marrow stromal cells can significantly expand much more primitive hematopoietic stem cells than AGM stromal cells only.

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    Effect of osteogenic growth peptide on gene expression changes in bone mesenchymal stem cells of OPG-/- mice: A Microarray analysis
    Miersalijiang Ya-sen, Guo Chang-jun, Fei Qin-ming, Chen Tong-yi, Cui Da-fu
    2011, 15 (27):  4975-4978.  doi: 10.3969/j.issn.1673-8225.2011.27.008
    Abstract ( 102 )   PDF (586KB) ( 355 )   Save

    BACKGROUND: Synthetic osteogenic growth peptide can stimulate proliferation and osteoblast differentiation of bone mesenchymal stem cells (BMSCs) in vitro, and which can enhance bone density in vivo, but the mechanism of the effect of osteogenic growth peptide (OGP) on BMSCs is not clear yet.
    OBJECTIVE: To investigate the effect of OGP on gene expression changes in BMSCs using mouse whole-genome microarray and to explore the gene and signal transduction pathway influenced by OGP.
    METHODS: Mouse whole-genome Oligo chip was obtained from Shanghai Bo Hao Biotechnology Co., Ltd., gene expression changes in BMSCs of OPG-/- in the OGP group (treated with OGP) and control group were screened. Real-time quantitative reverse transcriptase-polymerase chain reaction (RT-PCR) was used to analyze and verify gene expression changes related to proliferation and differentiation, and which combined with cluster analysis and pathway analysis to explore the mechanism of OPG.
    RESULTS AND CONCLUSION: Chip results showed that 346 genes expression down-regulated by OPG, 121 genes expression up-regulated. PCR validation results were consistent with the chip. Six pathways proteins were identified by BioCarta pathway analysis and 12 pathways were identified by KEGG pathway analysis. Multiple pathways were related to the mechanism of the effect of OGP on gene expression changes in BMSCs of OPG-/- mice, among which the MAPK signal transduction pathway may play an important role in their proliferation.

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    Multiple factors-induced differentiation of rat adipose tissue-derived stem cells into neuron-like cells
    Zhang Li-hua, Tang Yin-juan, Dong Wei-ren, Guo Jia-song, Chen Xiao-yan, Wang Hai-hong, Chen Pan-pan, Ye Quan-ying, Feng Shu-lan, Zhang Yi
    2011, 15 (27):  4979-4983.  doi: 10.3969/j.issn.1673-8225.2011.27.009
    Abstract ( 97 )   PDF (1364KB) ( 353 )   Save

    BACKGROUND: Differentiation of adipose tissue-derived stem cells (ADSCs) into neurons has been reported. However, little data are available regarding differential adhesion-purified ADSCs differentiation into neuron-like cells induced by multiple factors.
    OBJECTIVE: To explore the feasibility of inducing rat ADSCs into neuron-like cells with a new scheme and medium containing multiple factors.
    METHODS: ADSCs were isolated from the fat pads in groins and epididymis of male Sprague Dawley rats by enzyme digestion, and purified by differential attachment method. Fluorescent immunocytochemistry was used to identify the phenotype of the cells (CD44, CD49d and CD106 expressions). Differentiation of ADSCs into neuron-like cells was induced in cocktail-like neuronal differential medium containing insulin, hydrocortisone, valproic acid and forskolin. Also, fluorescent immunocytochemistry was used to identify the markers of the differentiated cells (Nestin and NeuN).
    RESULTS AND CONCLUSION: After sequentially isolated, purified and cultured, the obtained cells presented with long-fusiform shape, with clear nucleoli and light stained cytoplasm. They were positive for CD44 and CD49d, but negative for CD106. The application of NIM resulted in morphological changes of ADSCs during the first 6 hours, shown by pyramidal, irregular or triangular cell body with short, thin finger-like cell processes. After 24 hours of induction, most of the cells developed multiple branched processes resembling those of neurons and positive for Nestin and NeuN. Results showed that ADSCs could be induced to differentiate into neuron-like cells in cocktail-like neuronal differential medium.

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    Isolation, culture and osteogenic differentiation of human adipose-derived stem cells 
    Bai Wen, Yin Shuo, Cui Lei, Jiang Ming
    2011, 15 (27):  4984-4987.  doi: 10.3969/j.issn.1673-8225.2011.27.010
    Abstract ( 159 )   PDF (1129KB) ( 322 )   Save

    BACKGROUND: Adipose-derived stem cells (ADSCs) can secrete a large number of immune regulatory factors, not cause T-cell cytotoxicity, and adjust the type and quantity of T lymphocytes.
    OBJECTIVE: To establish a method for the isolation and culture of human ADSCs and to explore the ability of osteogenic differentiation.
    METHODS: ADSCs were isolated from the inguinal fat pads and digested with 0.1% type I collagenase, and cultured in osteogenic medium to study the osteogenic differentiation potential by using alkaline phosphatase staining, alizarin red staining and RT-PCR.
    RESULTS AND CONCLUSION: ADSCs could be expanded steadily in vitro and flow cytometry revealed high expression of stem cell-associated markers. The cytoplasm of the induced cells became black by alkaline phosphatase staining, the mineralized nodule became reddish-brown by alizarin red, RT-PCR detection of alkaline phosphatase positive expression. Human ADSCs are an ideal source of adult stem cells for use in the organization repair and cell therapy.

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    Biocompatibility of procine adipose derived stem cells and acellular dermal matrix
    Zhao Bao-cheng, Wang Zhen-jun, Han Jia-gang, Gu Bei, Xu Hui-min, Yu Xue-qiao
    2011, 15 (27):  4988-4992.  doi: 10.3969/j.issn.1673-8225.2011.27.011
    Abstract ( 71 )   PDF (1538KB) ( 346 )   Save

    BACKGROUND: Acellular dermal matrix has been widely used as a repair material in organ and tissue repair.
    OBJECTIVE: To investigate the biocompatibility of procine adipose derived stem cells and acellular dermal matrix.
    METHODS: Porcine adipose derived stem cells were obtained and cultured with collagenase digestion method. Flow cytometric analysis and adipogenic, octeogenic differentiation analysis were used to identify the stem cells.
    RESULTS AND CONCLUSION: The stem cells isolated from subcutaneous adipose tissue were positive for CD44 and CD105, negative for CD34 and CD45. After cultured in mesenchymal stem cell adipogenic and octeogenic differentiation basal medium respectively for 3 weeks, the cells were positive for oil red O staining and alizarin bordeaux staining. Both hematoxylin-eosin staining and scanning electron microscopy analyses confirmed that adipose derived stem cells could adhere to acellular dermal matrix. Adipose derived stem cells have good biocompatibility with acellular dermal matrix. Adipose derived stem cells-seeded acellular dermal matrix can be used in tissue engineering as a mechanical reconstructive agent and as a biolayer of stem cells for targeted delivery.

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    Effect of the cells attached to centrifugation tubes on the successful culturing rate of human umbilical cord blood mononuclear cells in vitro 
    Yin Wen-hua, Jin Da-di, Lu Kai-wu, Lei Ying
    2011, 15 (27):  4993-4997.  doi: 10.3969/j.issn.1673-8225.2011.27.012
    Abstract ( 119 )   PDF (1391KB) ( 300 )   Save

    BACKGROUND: A large number of mononuclear cells adhere to the centrifugation tube in the process of densitygradient centrifugation and isolation for the umbilical cord blood mononuclear cells (UCB-MNCs), the correlation between these adherent cells and the success rate of culturing UCB-MNCs in vitro remains unclear.
    OBJECTIVE: To compare the achievement ratio of cultivating UCB-MNCs in vitro by four different methods and to elucidate the influence of the cells adhering to the centrifugation tube on the cultivating rate of UCB-MNCs in vitro.
    METHODS: A total of 36 samples were obtained from umbilical cord blood of term deliveries and were divided randomly into four groups, with 9 samples in each. A group: methylcellulose isolation method; B group: density gradient centrifugation isolation method; C group: methylcellulose isolation method plus density gradient centrifugation; D group: methylcellulose isolation method plus modified density gradient centrifugation. Mononuclear cells were separated by the above four methods within 6 hours after collection, seeded in 25 cm2 culture flask at a concentration of 1×109/L - 2×109/L and suspended in low glucose-DMEM cell culture medium supplemented with 0.1 volume fraction of fetal bovine serum. The morphology was observed under contrast phase microscope. UCB-MNCs at passage 3 were collected and counted with cell counting plate. The amplification times were calculated. Flow cytometry was used to examine the surface antigen phenotype of the third passage cells.
    RESULTS AND CONCLUSION: There were 33 samples successfully isolated out of 36 UCB-MNCs samples, while three samples failed in B group. A large number of adherent cells were seen in 22 of 33 UCB samples (8 samples in Group A; 2 samples in Group B; 5 samples in Group C; 7 samples in Group D). Fibroblastoid cells from 9 samples (3 samples in Group A; 0 sample in Group B; 1 sample in Group C; 5 samples in Group D) were passaged steadily with the achievement ratio of 27.27%. Fibroblast-like cell and round megakaryocyte were the two basic types of adherent cells at 5-7 days after primary culture. At 3-4 weeks after serial subcultivation, UCB-MSCs could be found in A group and D group, they were morphologically similar to MSCs, showing homogeneous fusiform shape. These cells were cultured steadily for 60-90 days without obvious differences in morphology. Flow cytometry showed that, MSCs-related antigens such as CD29 and CD105 were expressed strongly on the surface of UCB-MSCs, but few hematopoietic lineage markers such as CD34 and CD45 nor endothelial markers such as CD106 could be found. Cells adhering to the centrifugation tubes may elevate significantly the achievement ratio of UCB-MSCs in vitro, methylcellulose isolation method combined with modified density gradient centrifugation could fully recover the adherent cells, thus benefiting for amplifying and passaging UCB-MNCs steadily in vitro.

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    Pyrroloquinoline quinone and proliferation of neural stem cells
    Xiong Shun-hua, Li Qing, Yao Bai-chun, Zhao Dan
    2011, 15 (27):  4998-5001.  doi: 10.3969/j.issn.1673-8225.2011.27.013
    Abstract ( 101 )   PDF (1143KB) ( 637 )   Save

    BACKGROUND: At present, scholars mainly used growth factor-like substance to promote the division and proliferation of neural stem cells. We assumed that pyrroloquinoline quinone (PQQ) micromolecular compound can accelerate the division and proliferation of neural stem cells.
    OBJECTIVE: To investigate the promoting effects of PQQ on the proliferation of rat adult neural stem cells in vitro. 
    METHODS: The neural stem cells of Wistar rat were cultured in vitro, and 1×10-8 mol/L PQQ was administered into the culture fluid. An equal volume of Hanks solution was added in the control group. The cell cycle was examined by the flow cytometry. The cyclin-dependent Kinase (CDK2) and cyclin-dependent kinase inhibitor (P27) expressions were detected by immunohistochemical staining and western blot assay.
    RESULTS AND CONCLUSION: Compared with the control group, after 16 and 24 hours of PQQ administered into the culture fluid, the rate of cells in S and G2 stage was increased and the apoptosis rate of cells was decreased markedly. The expression of CDK2 protein was noticeably increased, and the expression of P27 protein was decreased. Results suggest that low dose of PQQ could encourage the proliferation of the neural stem cells of rats.

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    Efficient method for establishing mouse embryonic fibroblast feeder layers
    La Xiao-lin, Tian Hai-qing, Cai Xia
    2011, 15 (27):  5002-5006.  doi: 10.3969/j.issn.1673-8225.2011.27.014
    Abstract ( 92 )   PDF (1709KB) ( 441 )   Save

    BACKGROUND: Mouse embryonic fibroblasts (MEFs) feeder is more frequently used to culture embryonic stem cells (ESCs) and can retain ESCs proliferative potential in an undifferentiated state. But the preparation of feeder cells is elaborate and multiplicity.
    OBJECTIVE: To develop a simple and efficient method to establish MEFs feeder layers in vitro.
    METHODS: Mouse fetuses of 13.5-day gestational age were chosen to isolate MEFs as feeder layer. MEFs were isolated using two simply methods in vitro. The change of cells about appearance and amount was observed by inverted microscope; frozen MEFs were thawed through different methods, and the survival rate of MEFs was contrasted. MEFs were inactivated with different concentration mitomycin C and different time treatment to prepare MEFs feeder layer.
    RESULTS AND CONCLUSION: The primary MEFs isolated using the two simple methods were in the best state and adequate. The two methods were better to culture primary mouse embryonic fibroblast cells, and complex manipulate protocol could be avoided. After thawed by the simple method, MEFs were treated with 10 mg/L mitomycin C for 1.5-2.0 hours or 1 mg/L mitomycin C overnight based on different confluence conditions.

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    Isolation and identification of improved human peripheral peritoneum mesothelial cells
    Yin Li-bo, Zhao Wen-xiu, Yin Zhen-yu, Wang Xiao-min
    2011, 15 (27):  5007-5010.  doi: 10.3969/j.issn.1673-8225.2011.27.015
    Abstract ( 100 )   PDF (1050KB) ( 339 )   Save

    BACKGROUND: Peripheral peritoneum mesothelial cells are served as an important component of peritoneum which secrete many kinds of cytokines, and play an important role in anti-inflammatory, immunoloregulation, and peritoneal fibrosis. How to obtain high-quality and homogeneous peritoneal mesothelial cells has become the key to solving problems.
    OBJECTIVE: To develop an improved method for digestion culture of human peritoneal mesothelial cells (HPMCs).
    METHODS: HPMCs were digested by 0.1% collagenaseⅠ, after eliminating erythrocytes, the cells were cultured by 10% fetal bovine serum of 1640 medium. Inverted microscope was used to observe the morphological structures of cells; CCK-8 was used to test the promotion of medium on the growth of mesothelial cell. The ultrastructure of cells was observed by transmission electron microscope (TEM), and isolated cells were identified by laser confocal immunofluorescence microscope.
    RESULTS AND CONCLUSION: The isolated and cultured mesothelial cells were polygonal and confluenced gradually and grew well like the slab stone. The purity of cultured mesothelial cells was more than 90%; the cells grew well, quickly, and could be passaged to 4 and 5 generations. Microvilli of the cells were evident on the surface of cells under TEM. Immunofluorence analysis showed the cells were positively express cytokeratin and vimentin, but negative for leucocyte CD45 and factor Ⅷ fos-related antigen. All identified marks are accorded with the characteristics of mesothelial cells. The results indicated that collagenaseⅠdigestion method is simple, efficient, and reproducible separation method of HPMCs.

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    Influence of autologous bone marrow mononuclear cells transplantation on SDF-1-CXCR4
    Zhang Yun-qiang, Xu Ai-guo, Qi Xiang-qian
    2011, 15 (27):  5011-5015.  doi: 10.3969/j.issn.1673-8225.2011.27.016
    Abstract ( 98 )   PDF (695KB) ( 416 )   Save

    BACKGROUND: Recently, the SDF-1-CXCR4 mRNA expression and the effect after stem cell transplantation have obtained more attention.
    OBJECTIVE: To observe the changes of SDF-1 mRNA and CXCR4 mRNA expression in the myocardium after bone marrow mononuclear cells (BM-MNCs) transplantation.
    METHODS: Sixteen mongrel dogs were randomly divided into the graft group and the control group. Each of dog was implanted a permanent pacemaker for rapid right ventricular pacing for 3 to 4 weeks. CM-DiI 1abled BM-MNCs or saline were transplanted into the myocardium via epicardium injection.
    RESULTS AND CONCLUSION: After 3-4 weeks of rapid pacing, the cardiac function of the dogs in both two groups significantly decreased in hemodynamic and in ultrasound parameters. The mRNA levels of SDF-1 and CXCR4 were higher in the graft group than those in the control group (P < 0.01). Autologous BM-MNCs transplantation improves the mRNA level of SDF-1 and CXCR4.

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    Experimental study and short-term clinical follow-up of bone mesenchymal stem cells transplantation for repair of spinal cord injury  
    Gao De-xuan, Jia Quan-zhang, Li Dong-jun, Chen Yu-bing, Sun Jing-hai, Wang Feng-hua, Xu Shuang, Liu Li-ping, Jiang Da-wei
    2011, 15 (27):  5016-5020.  doi: 10.3969/j.issn.1673-8225.2011.27.017
    Abstract ( 102 )   PDF (576KB) ( 400 )   Save

    BACKGROUND: Studies of bone marrow mesenchymal stem cells (BMSCs) have gradually experienced a transition from animal experiments to clinical application. However, the mechanism is still unclear.
    OBJECTIVE: To observe the repairing effect and short-term effect of BMSCs transplantation on rats motor function.
    METHODS: Spinal cord injury models were prepared by modified Allen’s crack method; the BMSCs which were isolated and cultured in vitro were transplanted into the model through the vena caudalis and the local lesion. The behavioral changes were observed using the modified Tarlov score standard and the pathological changes under the light microscope. Five patients with spinal cord injury were transplanted autologous BMSCs via in suit injection, lumbar puncture and venous injection. Neurologic function and ability of daily living were evaluated.
    RESULTS AND CONCLUSION: After 15 days, there was a significant increase in the score of motion function of rats receiving BMSCs transplantation as compared with the control group. Through observing the spinal pathological section after transplantation, there was significantly more recovery in the BMSCs group than the model group at post-transplantation 7, 15, 30 days. After 6 months of short-term observation, the neurologic function and ability of daily living were improved in patients undergoing BMSCs transplantation.

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    Vein transplantation of olfactory ensheathing cells for spinal cord injury
    Wei Kai-bin, Liu Yu-liang, Liu Hong, Lü Xin-gang, Zhang Wen-zheng, Li Jun
    2011, 15 (27):  5021-5025.  doi: 10.3969/j.issn.1673-8225.2011.27.018
    Abstract ( 111 )   PDF (411KB) ( 354 )   Save

    BACKGROUND: Olfactory ensheathing cell transplantation is a better theray for spinal cord injury, and it becomes one of the most promising treatment methods. Local transplantation is applied currently, with the disadvantages of complex operation, large trauma, repeated transplantation. Looking for a simple and effective way for cell transplantation becomes a hotspot for scholars from various countries.
    OBJECTIVE: To investigate the effect and possibility of transplantation of olfactory ensheathing cells for treatment of spinal cord injury.
    METHODS: Wistar rats with T10 spinal cord hemisection were divided into 4 groups: intramedullary local transplantation group (A), vein transplantation group (B), D/F12 transplantation group (C) and control group (D). The functional recovery of rats with spinal cord injury was observed with combined behavioral score at different phases. The tissue sections of each group were made at 5 and 10 weeks postoperatively to observe the axon regeneration and the survival of olfactory ensheathing cells.
    RESULTS AND CONCLUSION: The experiment showed that the rats transplanted with OECs at injured site and through the vein had more improvement in functional recovery and histological changes than the other two groups. The effect between A group and B group had not significant difference. The method of treating spinal cord injury by transplanting OECs via the vein not only simplifies the operation and avoids many complications but also has good curative effect similar to local transplantation.

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    Influence of tail vein administration of bone marrow mesenchymal stem cells on expression of brain-derived neurotrophic factor and nerve growth factor after spinal cord injury in rats
    Dong Feng, Lin Jian-hua, Wu Zhao-yang
    2011, 15 (27):  5026-5030.  doi: 10.3969/j.issn.1673-8225.2011.27.019
    Abstract ( 93 )   PDF (1342KB) ( 383 )   Save

    BACKGROUND: Transplantation of bone marrow mesenchymal stem cells has an effect on the treatment of spinal cord injury, but the mechanism is not fully understood.
    OBJECTIVE: To explore the influence of intravenous administration of bone marrow mesenchymal stem cells on expression of brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) after spinal cord injury in rats and to study possible mechanism of intravenous administration of bone marrow mesenchymal stem cells after spinal cord injury in adult rats.
    METHODS: Modified Allen method was applied to induce T10 spinal cord injury to prepare rat models of paraplegia. There were 6 rats in sham operation group and 24 rats in injury group. Then, the injury group was randomly divided into transplantation group and control group. Rats in the sham operation and transplantation groups received tail vein transplantation of 1 mL bone marrow mesenchymal stem cells (1×106 cells), while those in the control group were treated with PBS.
    RESULTS AND CONCLUSION: After spinal cord injury in rats, the expression of BDNF and NGF was improved and advanced to increase via intravenous administration of bone marrow mesenchymal stem cells. Maybe it is one of the mechanisms of promoting restoration of injured spinal cord and improving motor function.

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    Isolation, culture and identification of rat hair follic stem cells
    Wang Zhu-qian, Muratrixat, Li Jia, Wang Yu-jie
    2011, 15 (27):  5031-5034.  doi: 10.3969/j.issn.1673-8225.2011.27.020
    Abstract ( 100 )   PDF (1391KB) ( 823 )   Save

    BACKGROUND: Hair follicle stem cells (HFSCs) based on in vivo role of the bladder and surrounding tissue environment are likely to differentiate into urothelial cells and smooth muscle cells, which become a new stem cell research.
    OBJECTIVE: To investigate an effective and simple method of isolation, culture and identification of rat HFSCs.
    METHODS: After sterling, the skin of the rat’s beard was cut off, the vibrissa follicles were dissected under a stereocroscope. The dermal sheath was moved by incubated in Dispase Ⅱ firstly, second step with a mixture of trypsin and EDTA. The cells suspension was cultured in 10% fetal bovine serum keratinocyte free serum medium and selected by rapid adhering on collagen Ⅳ. The cultured cells were passaged, when cells were confluent with 70%-80%. Selected cell microstruture was observed under optics microscope and electron microscopy respectively. Cells were characterized by flow cytomitry with antibody against CD34 and β1-integrin.
    RESULTS AND CONCLUSION: The selected HFSCs were uniform in shape, more refraction, cobblestone-morph by optics microscope. The form was primitive, small ratio of nucleus and cytoplasm, obvious nucleolus, organelle of developmental immaturity by transmission electron microscope. In adherent cells (experiment groups), CD34 and β1-integrin expression rate was (39.52±19.57)% and (93.46±4.73)%, respectively. In no-adherent cells (control groups) was corresponding (19.20±11.53)% and (63.57±14.42)% respectively. There was a significant difference between two groups (P < 0.05). Highly purified HFSCs can be obtained by dissection under a stereocroscope and two-step enzyme digestion combining with rapid adhering on collagen Ⅳ. CD34 combined with β1-integrin are an ideal marker to identify HFSCs.

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    Immunosuppression of allogeneic bone marrow-derived mesenchymal stem cells-induced osteoblasts on T cells in mixed lymphocyte culture system
    Pan Rong-gui, Fan Qie, Deng Yao-liang, Zhao Jin-min
    2011, 15 (27):  5035-5038.  doi: 10.3969/j.issn.1673-8225.2011.27.021
    Abstract ( 74 )   PDF (1256KB) ( 334 )   Save

    BACKGROUND: Results of immunclogical response of allogeneic bone marrow-derived mesenchymal stem cells-induced osteoblast transplantation are varied.
    OBJECTIVE: To investigate the features of immune adjustment function derived from the interaction of osteoblasts derived from mesenchymal stem cells (ODCs) with T cells in vitro.
    METHODS: Rabbit bone marrow mononuclear cells were isolated by Ficoll-Hypaque density gradient, ex vivo culture-expanded, and obtained after the third passage. The classic chemical induced ODCs at different proportion were added to T cells to form two-way mixed lymphocyte culture system. At 3, 5, 7 days, MTT assay was used to detect T cell proliferation in each group. T-cell subsets apoptosis was analyzed using flow cytometric analysis after 24 hours.
    RESULTS AND CONCLUSION: ODCs inhibited T cell proliferation in a dose-effect manner in a certain range. With increasing ODC dose and time, inhibition was enhanced. Comparison of mean inhibition rate of three times showed that (1: 20) group was less than (1: 80) group, and (1: 40) group was less than (1: 80) group (P < 0. 05). ODCs can cause apoptosis of T cell subsets, including CD4+ (apoptosis rate 8.57%) subtypes less than CD8+ (apoptosis 15.31%; P < 0.01). Results showed that ODCs in vitro can suppress T cells proliferation through pathway of cell apoptosis, especially for CD8+. However, this inhibition is not particularly strong, showing that the ODCs have some degree of immunity, but it is very low.

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    Effect of peripheral blood mesenchymal stem cells transplantation on neovascularization and cardiac function of myocardial infarction rabbits
    Liu Zhi-jiang, Shi Bei, Zhao Ran-zun, Shen Chang-ying, Wang Dong-mei, Wang Zheng-long
    2011, 15 (27):  5039-5043.  doi: 10.3969/j.issn.1673-8225.2011.27.022
    Abstract ( 101 )   PDF (1855KB) ( 476 )   Save

    BACKGROUND: Both Drug treatment and percutaneous coronary intervention cannot repair the necrotic myocardium following myocardial infarction.
    OBJECTIVE: To investigate the effect of peripheral blood mesenchymal stem cells (MSCs) transplantation on the neovascularization and cardiac function following myocardial infarction in rabbits.
    METHODS: Thirty-six New Zealand rabbits were divided into MSCs transplantation group (n=12), control group (n=12) and sham operation group (n=12). Rabbits models of acute myocardial infarction were established in the former two groups.
    RESULTS AND CONCLUSION: Flow cytometry demonstrated that most MSCs expressed CD44, very few cells expressed CD34 and CD45 at 4 weeks after cell transplantation. Transplanted MSCs could survive in infarcted myocardium. Left ventricular ejection fraction and left ventricular fractional shortening of the MSCs transplantation group were higher significantly than those of the control group (P < 0.01). Left ventricular end-systolic diameter and end-diastolic diameter were lower significantly in the MSCs transplantation group than the control group (P < 0.01). Myocardial fibrosis and myocardial infarct size were lower significantly in the MSCs transplantation group than the control group (P < 0.01). Capillary density was increased significantly in the MSCs transplantation group compared with the control group (P< 0.01). Peripheral blood MSCs transplantation increases new capillary density in infarcted myocardium and improves cardiac function.

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    Effects of granulocyte colony-stimulating factor on neural cell apoptosis in the hippocampus of vascular dementia rats
    Li Xiao-yun, Lan Xi-fa
    2011, 15 (27):  5044-5047.  doi: 10.3969/j.issn.1673-8225.2011.27.023
    Abstract ( 93 )   PDF (607KB) ( 592 )   Save

    BACKGROUND: The study found that granulocyte colony stimulating factor (G-CSF) can activate adult neural stem cells of the brain, stimulate their proliferation and differentiation, but also promote the secretion of varieties of neurotrophic factors of the brain, reduce ischemic lesions in the animal model of cerebral ischemia, and promote the long-term recovery of missing neurological function in chronic brain stroke models.
    OBJECTIVE: To investigate the effect of G-CSF on the apoptosis of neural cells of the hippocampus of rats with vascular dementia.
    METHODS: Rats were treated with a permanent bilateral occlusion of both common carotid arteries (2-VO) for establishing vascular dementia model. In the experimental group, the rats were given G-CSF by subcutaneous injection. In the control group, the rats were treated with saline. In the sham surgery group, an incision was made at midline of the neck, without ligation of common carotid artery. Morris water maze test was conducted to perform the oriented navigation and to observe escape latency in rats, and to assess the spatial learning and memory abilities. Neuronal cell apoptosis in the hippocampus of rats was investigated by TUNEL staining and image analysis.
    RESULTS AND CONCLUSION: Compared with the sham surgery group, the average escape latency of rats was significantly longer in the control and experimental groups at 7 days following cerebral ischemia (P < 0.01). The number of TUNEL positive neurons in the hippocampus was significantly greater in the control and experimental groups compared with the sham surgery group (P < 0.01). With prolonged time, the learning and memory abilities became gradually severe and the number of TUNEL-positive cells gradually increased on days 14 and 28. The average escape latency of rats was significantly shorter in the experimental group compared with the control group on days 14 and 28. The number of TUNEL-positive cells in the hippocampus was significantly reduced in the experimental group compared with the control group. These indicated that treatment of exogenous G-CSF at early stage following cerebral ischemia contributes to the decrease in apoptosis of neural cells in the hippocampus and improves the learning and memory abilities in rats.

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    Differentiation of rabbit mesenchymal stem cells into cartilage phenotype induced by transforming growth factor beta 3  
    Sui Lai-jian, Lü Cheng-yu, Zhang Hai-ning, Xu Hao, Gao Zheng-yu, Sui Ai-hua, Wang Ying-zhen
    2011, 15 (27):  5048-5052.  doi: 10.3969/j.issn.1673-8225.2011.27.024
    Abstract ( 95 )   PDF (709KB) ( 423 )   Save

    BACKGROUND: Endogenous induction of cartilage differentiation is to use a certain carrier to integrate the target genes into stem cells to induce self-differentiation by self-induced secretion of cytokines.
    OBJECTIVE: To observe the ability of rabbit bone marrow mesenchymal stem cells (BMSCs) transfected with transforming growth factor beta 3 (TGF-β3) to differentiate into cartilage phenotype through adeno-associated virus vector.
    METHODS: The third passage BMSCs in logarithmic growth phase was transfected by rAAV2-TGF-β3. Total protein was extracted from cells at 3, 6, 9, 12 days after transfection, and TGF-β3 was detected through ELISA. After 2 weeks of culturing, mRNA expressions of type Ⅱ collagen were determined by RT-PCR and the collagen Ⅱ protein was detected by western blot. The expression of proteoglycan was shown by toluidine blue staining.
    RESULTS AND CONCLUSION: After transfection, BMSCs can express TGF-β3 stably, and make a better cartilage transformation compared to negative control group. TGF-β3 can be transfected into BMSCs through adeno-associated virus vectors and induce cell differentiation into cartilage phenotype.

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    Hemeoxygenase-1 expression effect on the up-regulation of peripheral blood CD4+CD25+CD127low/- regulatory T cells mediated by mesenchymal stem cells in asthma patients 
    Wen Bing, Zhuansun Yong-xun, Yan Fu-de, Chen Rui, Zhang Wei, Feng Su-ling, Li Jian-guo
    2011, 15 (27):  5053-5057.  doi: 10.3969/j.issn.1673-8225.2011.27.025
    Abstract ( 103 )   PDF (653KB) ( 283 )   Save

    BACKGROUND: Up-regulating CD4+CD25+CD127low/- regulatory T cells is a new target in the treatment of asthma. Human bone marrow mesenchymal stem cells (MSCs) can up-regulate CD4+CD25+CD127low/- regulatory T cells in vitro, while the mechanism is not clear.
    OBJECTIVE: To study the effect of hemeoxygenase-1 (HO-1) expression in the up-regulation of peripheral blood CD4+CD25+CD127low/- regulatory T cells mediated by MSCs in asthma patients.
    METHODS: Real-time PCR was used to examine the expression of HO-1 mRNA in MSCs pretreated with 0, 15, 30, 45, 60 μmol/L Hemin (the revulsive of HO-1) and 0, 5, 10, 15, 20 μmol/L ZnPP (the inhibitor of HO-1) respectively. Peripheral blood mononuclear cells (PBMCs), which were isolated from 10 cases of asthma patients with acute episode and 10 cases of healthy controls using Ficoll density gradient centrifugation, were incubated with MSCs pretreated with Hemin, ZnPP and mock respectively.
    RESULTS AND CONCLUSION: The expression of HO-1 in MSCs can be induced and inhibited in vitro. The higher concentration of Hemin added to MSCs, the higher expression of HO-1 mRNA was tested (P < 0.05). With the increasing concentration of ZnPP added to MSCs, the expression of HO-1 mRNA was becoming lower (P < 0.05). The proportion of CD4+CD25+CD127low/- regulatory T cells in CD4+ T cells could be up-regulated by MSCs (P < 0.01) and also by MSCs with induction of HO-1 expression (P < 0.01). While MSCs with inhibition of HO-1 expression could down-regulate the proportion of CD4+CD25+CD127low/-regulatory T cells in CD4+ T cells (P < 0.01). The expression of HO-1 partially contributed to the up-regulation of CD4+CD25+CD127low/- regulatory T cells mediated by MSCs in asthma patients.

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    In vitro effect of stromal cell derived factor -1 on the migration of neural stem cells
    Mu Lin-jie, Ding Peng, Wang Chong-qian, Wang Wei-min, Li Xuan-peng, Wang Jin-kun
    2011, 15 (27):  5058-5062.  doi: 10.3969/j.issn.1673-8225.2011.27.026
    Abstract ( 132 )   PDF (1490KB) ( 516 )   Save

    BACKGROUND: Neural stem cell migration plays important roles in the development and repair of the central nervous system. Although recent studies have shown that the chemokines mediate neural stem cell migration, but the mechanism is unclear.
    OBJECTIVE: To explore the effects of stromal cell-derived factor-1 (SDF-1) on migration of fetal rat hippocampus neural stem cells in vitro.
    METHODS: The fetal rat hippocampal neural stem cells were isolated, cultured and identified in serum-free medium. The expression of CXCR4 in neural stem cells was detected using immunofluorescence and RT-PCR. The under-agarose cell migration assay was used to observe the effects of SDF-1(50-500 ng/ml) on neural stem cell migration, and blocking CXCR4, the receptor of SDF-1, to identify the specificity of migration.
    RESULTS AND CONCLUSION: Immunofluorescence results showed that neural stem cells were CXCR4 positive, and RT-PCR findings showed 643 bp specific band in agarose gel electrophoresis. The Under-Agarose cell migration assay showed that: SDF-1 (50-500 ng/ml) could accelerate the migration of neural stem cells, the migration increased with the concentration, and 500 μg/L was the best. By adding anti-CXCR4 polyclonal antibodies, the migration of neural stem cells compared with SDF-1 was significantly reduced, no significant difference with the control group (P > 0.05), pointing out anti-CXCR4 polyclonal antibodies can block the effect of the migration.

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    Expression of stromal cell-derived factor-1 after articular cartilage injury
    Lu Ding-gui, Wei Qing-jun, Li Qiao-chuan, Wei Ji-hua, Xiao Shi-hui, Li Wei-an
    2011, 15 (27):  5063-5067.  doi: 10.3969/j.issn.1673-8225.2011.27.027
    Abstract ( 83 )   PDF (1593KB) ( 378 )   Save

    BACKGROUND: Studies have demonstrated that stromal cell-derived factor-1 (SDF-1) can influence the migration and aggregation of bone marrow mesenchymal stem cells (BMSCs).
    OBJECTIVE: To observe the expression of SDF-1 at lesion regions at different time after cartilage injury and to investigate the correlation between SDF-1 expression and BMSCs migration.
    METHODS: Rabbits models of articular cartilage injury were established. Focal osteochondral lesions were collected 2, 5, 7, 10, 14 and 28 days after injury. The influence of SDF-1 expression on the migration of BMSCs and chondrocytes was observed.
    RESULTS AND CONCLUSION: SDF-1 expression was significantly increased and peaked at the seventh day (P < 0.05). BMSCs migrated toward articular cartilage injury tissue, while they were significantly inhibited by the inhibitor of CXCL4. SDF-1 expression increases in the early phase after articular cartilage injury, and plays an important role in chemoattracting MSCs to injured lesions.

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    Mannitol improves the efficacy of intravenous transplantation of human umbilical cord blood CD34+ cells for cerebral infarction in hypertensive rats
    Yu Guo-long, Ou Ya-li, Yang Tian-lun, Fang Li, Hu Ke
    2011, 15 (27):  5068-5071.  doi: 10.3969/j.issn.1673-8225.2011.27.028
    Abstract ( 115 )   PDF (1273KB) ( 245 )   Save

    BACKGROUND: Intravenous transplantation of human umbilical cord blood cells (HUCBCs) in treatment of cerebral infarction is limited. Only a small fraction of the grafted cells appears to survive at the damaged brain and the behavioral recovery is only partial.
    OBJECTIVE: To evaluate the ability of Mannitol, a blood brain barrier (BBB) permeabilizer, to enhance neuroprotective effects of intravenously administered HUCBCs for cerebral infarction in spontaneous hypertensive rats.
    METHODS: CD34+ cells isolated from HUCB were transfected by GFP plasmid with liposome method. Forty-five adult male spontaneous hypertensive rats with middle cerebral artery occlusion were randomly divided into three groups at 24 hours after modeling, each of 15: Experimental group, GFP-CD34+ cells (1×106) and 20% Mannitol (2 g/kg) were administrated intravenously at 24 hours after modeling; Positive control group, GFP-CD34+ cells (1×106) were only injected intravenously at same time; Blank control group, normal saline was injected at same time.
    RESULTS AND CONCLUSION: ①The number of GFP positive cells in cerebral tissues in the experimental group was increased significantly compared to the positive control group. ②No significant difference was found in the neurologic function scores at day 7 after transplantation among the three groups; but at day 28 after transplantation, the neurologic function in the experimental group was improved significantly compared with the positive or blank control group (P < 0.05). ③The cerebral infarct volume in the experimental group was significantly decreased compared with the positive or blank control group. ④The glial cell line-derived neurotrophic factor level in cerebral tissue in the experimental group was significantly increased compared with the positive and blank control groups. The results suggested that Mannitol enhanced CD34+ cells to migrate into ischemic-injured cerebral tissues, and to improve the efficacy of CD34+ cells delivered intravenously for cerebral infarction in spontaneous hypertensive rats.

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    Regulatory effect of connexin/gap junction intercellular communication on proliferation of rat hepatic oval cells 
    Fu Hua-qun, Li Xue-dong, Wang Kai-yang, Jiang Xing-xing, Chao Ying-hui
    2011, 15 (27):  5072-5075.  doi: 10.3969/j.issn.1673-8225.2011.27.029
    Abstract ( 149 )   PDF (1196KB) ( 306 )   Save

    BACKGROUND: Gap junction intercellular communication (GJIC) mediated by connexin (CX) is the pivotal pattern of communication in multicellular organism.
    OBJECTIVE: To observe the regulatory effect of CX/GJIC on hepatic oval cell proliferation.
    METHODS: Wistar rats were assigned to four groups. Control group received normal diet. Animal models of hepatic oval cell proliferation were established in the 2-acetylaminofluorene/ partial hepatectomy (2-AAF/PH) group according to modified Solt-Farber method. Phenobarbital group received phenobarbital drinking for 7 days, and on day 8, models were established as the 2-AAF/PH group. Phenobarbital drinking lasted till the end of the test. Panax notoginseng saponins (PNS) group received PNS 25 mg/kg daily by intraperitoneal injection during model establishment as the 2-AAF/PH group, lasting till the end of the test.
    RESULTS AND CONCLUSION: The patterns of CX expression were different in spatial and temporal in the rat liver after 2-AAF/PH, decreased and then recovered. The CX43 protein was expressed in hepatic oval cells, and they were increased at first and then to recover. GJIC was inhibited by altered the spatial and temporal expression patterns of CX in the rats liver after 2-AAF/PH (with phenobarbital) that can accelerate the proliferation of hepatic oval cells. GJIC was increased by enhancing the expression level of CX in the rats liver after2-AAF/PH (with PNS) that can accurately activate hepatic oval cells proliferation. The peak of hepatic oval cells proliferation was decreased, delayed and lasted long time. To decrease the GJIC in the rat liver of 2-AAF/PH that can accelerate and enhance the proliferation of hepatic oval cells, whereas to increase the GJIC can decrease, delay and last long time the proliferation of hepatic oval cells. These suggest that the proliferation and differentiation of hepatic oval cells were modulated by CX/GJIC.

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    Effect of GinsenosideRb1 and beta-amyloid 25-35 on tau phosphorylation in differentiated neural stem cells
    Zhao Qing-xia, Liu Xiao-zhuan, Li Bo, Yan Wen-hai, Han Xue-fei, Xing Ying
    2011, 15 (27):  5076-5079.  doi: 10.3969/j.issn.1673-8225.2011.27.030
    Abstract ( 95 )   PDF (671KB) ( 655 )   Save

    BACKGROUND: Currently, neural stem cells (NSCs) transplantation effect on the treatment of Alzheimer’s disease is improved by adjusting tau protein phosphorylation level during the differentiation of NSCs.
    OBJECTIVE: To explore the effect of GinsenosideRb1 and beta-amyloid 25-35 (Aβ25-35) on tau phosphorylation after NSCs are transformed into neurons.
    METHODS: NSCs were isolated and cultured from rat hippocampus. NSCs of the third passage were induced towards neurons after one week; the expression of Tau[pS396], Tau[pS262] and GSK-3β[pTyr279, 216] were tested by the immunofluorescent cytochemical staining and western-blot.
    RESULTS AND CONCLUSION: The expression of Tau[pS396], Tau[pS262] and GSK-3β[pTyr279, 216] was found in the process of NSCs differentiation. Aβ25-35 could enhance their expression; moreover Ginsenoside Rb1 could reverse the effect of Aβ25-35. The results indicated that there was a certain level of phosphorylation in tau protein during NSCs differentiation. Aβ25-35 and GinsenosideRb1 could regulate the level of tau phosphorylation. The mechanism of its action is by adjusting GSK-3β activity.

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    Aescine sodium combined with umbilical cord mesenchymal stem cells transplantation for treatment of neurological function in rats with cerebral infarction
    Chen Xue-fei, Mo Wan-bin
    2011, 15 (27):  5080-8084.  doi: 10.3969/j.issn.1673-8225.2011.27.031
    Abstract ( 130 )   PDF (635KB) ( 396 )   Save

    BACKGROUND: The effect of single umbilical cord derived mesenchymal stem cells (UC-MSCs) transplantation repair damaged brain tissue is not very satisfactory.
    OBJECTIVE: To investigate the effect of UC-MSCs transplantation combined with aescine sodium on the treatment of cerebral infarction in rats.
    METHODS: The models of cerebral infarction were made by middle cerebral artery occlusion (MCAO). Rats were divided randomly into control group, UC-MSCs group and Aescine sodium + UC-MSCs group. The concentration of 1×1010/L UC-MSCs suspension or the concentration of 1 mL cell culture fluid was injected into MCAO models through caudal vein, at the same time,
    5 mg/(kg•d) aescine sodium aqueous solution or normal saline was injected into MCAO models through abdominal cavity, for 5 days.
    RESULTS AND CONCLUSION: The neurological dysfunction scores in aescine sodium + UC-MSCs group were significantly lower than those in UC-MSCs group and control group at 1 week after transplantation (P < 0.05). RT-PCR approved that the expression of AQP4 and AQP9 mRNA was highest in control group, a few in UC-MSCs group and lowest in aescine sodium + UC-MSCs group (P < 0.05). The number of CM-Dil-positive cells and neurons in aescine sodium + UC-MSCs group was higher than that in UC-MSCs group and control group (P < 0.05). The results suggested that UC-MSCs transplantation combined with aescine sodium can significantly improve neurological function of rats with cerebral infarction.

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    Isolation, culture and biological characteristics of cancer stem cells
    Wang Rui-hai
    2011, 15 (27):  5087-5090.  doi: 10.3969/j.issn.1673-8225.2011.27.033
    Abstract ( 97 )   PDF (565KB) ( 923 )   Save

    BACKGROUND: Cancer stem cells are a kind of seed cells with self-renewal capacity and uncertain differentiation potential, and can differentiate into tumor cells to different extents, which are the root cause of continued growth, metastasis and recurrence of malignant tumors which cannot be completely killed by traditional chemotherapy.
    OBJECTIVE: To review the isolation, culture and biological characteristics of cancer stem cells.
    METHODS: A computer retrieve of Wanfang database (1990-01/2010-12) was conducted for articles regarding the isolation, culture and biological characteristics of cancer stem cells using the keywords of “cancer stem cells, isolation and culture, biological characteristics” in Chinese. Repetitive articles, reviews and Meta analyses were excluded, and finally 22 of 45 articles were included in result analysis.
    RESULTS AND CONCLUSION: CD133 is regarded as a specific marker of cancer stem cells in various organ tumors, including lung cancer, pancreatic cancer, colon cancer, hepatocellular carcinoma, nervous system tumors. Nestin, vimentin, and CD117 express in cancer stem cells of the nervous system. Expressions of CD44 and endothelin-converting enzyme in lung cancer stem cells are of significance. CD44 and CD24 can be used as cancer stem cell surface markers for sorting human pancreatic cancer cell line PANC-1. CD166 has a high expression in colorectal cancer stem cells.

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    Research development of Hedgehog signal pathway and proliferation and differentiation of related stem cells
    Wang Li,Yang Zhi-yun, Wang Xian-bo
    2011, 15 (27):  5091-5095.  doi: 10.3969/j.issn.1673-8225.2011.27.034
    Abstract ( 85 )   PDF (680KB) ( 377 )   Save

    BACKGROUND: Hedgehog protein is morphogen, and the signal pathway which is related to Hedgehog protein takes part in the embryogenesis and proliferation and differentiation of adult tissues.
    OBJECTIVE: To review the proliferation and differentiation of stem cells related to Hedgehog signal pathway.
    METHODS: The articles related to Hedgehog signaling pathway in CNKI database and PubMed Database from January 2000 to December 2010 were retrieved with the key words of “Hedgehog signaling pathway, cell proliferation, cell differentiation, signal pathway controlling”. The articles related to the function of Hedgehog signaling pathway to several kinds of stem cells and adult organs were selected. A total of 169 literatures were obtained from computer screen, and 27 documents of them were involved for summarization according to inclusion criteria.
    RESULTS AND CONCLUSION: Stem cells with multiple differentiation potential developed into histiocytes with special biological function were regulated by stem cells or external, short-range or long-range signal. Intercellular information transfer plays an important role in the development and differentiation of cells. Hedgehog signal pathway can maintain the balance of cell proliferation, differentiation and apoptosis, and can regulate molecular difference among flanking cells, and play a crucial effect on cell differentiation.

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    Roles of MicroRNA in regulating proliferation and differentiation of stem cells
    Qi Shao-hua, Wu Dong-cheng, Li Dong-sheng
    2011, 15 (27):  5096-5099.  doi: 10.3969/j.issn.1673-8225.2011.27.035
    Abstract ( 80 )   PDF (498KB) ( 472 )   Save

    BACKGROUND: MicroRNAs (miRNAs) have an important role in regulating stem cell self-renewal and differentiation by repressing the translation of selected mRNAs in stem cells.
    OBJECTIVE: To investigate the roles of miRNAs in regulating proliferation and differentiation of stem cells.
    METHODS: The first author searched PubMed database, Elsevier database and Nature database from 2000 to 2010. Key words were “stem cell, embryonic stem cell (ESC), induced pluripotent stem cell (iPS cell), microRNA (miRNA)”. Duplicated articles were excluded. Finally, 39 articles were selected.
    RESULTS AND CONCLUSION: MicroRNAs are specifically expressed in embryonic stem cells. MiRNAs play important roles in regulating stem cell’s proliferation and differentiation. MiRNAs modulate multiple stages and cell types of hemopoietic stem cell differentiation. MiRNAs also regulate the differentiation of neural stem cells, mesenchymal stem cells and skin stem cells. Embryonic stem cell-specific miRNAs promote the efficiency of somatic cell reprogramming.

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    Platelet lysate on the proliferation and differentiation of umbilical cord mesenchymal stem cells
    Sun Wei-xue, Sun Kang, Tian Shao-qi, Xing Shi-chao
    2011, 15 (27):  5100-5103.  doi: 10.3969/j.issn.1673-8225.2011.27.036
    Abstract ( 102 )   PDF (658KB) ( 524 )   Save

    BACKGROUND: In recent years, umbilical cord mesenchymal stem cells (UCMSCs) are one of significant cells in stem cell biology. UCMSCs have a good prospect in the field of cell therapy. Platelet lysate has varying degrees of beneficial effect for proliferation and differentiation of stem cells. To a certain extent, it can replace or even is better than the serum in the culture medium.
    OBJECTIVE: To summarize the studies regarding platelet lysate combined with UCMSCs.
    METHODS: Literatures can be searched with keywords like umbilical cord, mesenchymal stem cells, platelet lysate, proliferation and differentiation in Chinese databases such as Wanfang and English databases such as PubMed. The biological characteristics and clinical practice of UCMSCs and platelet lysate were summarized. Studies regarding the effect of platelet lysate on the proliferation and differentiation of UCMSCs were included.
    RESULTS AND CONCLUSION: Platelet lysate plays a positive role on the proliferation and differentiation of UCMSCs, thus indicating a significant role in the stem cell transplantation.

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    Research progress of adipose-derived stem cells inducing epidermal cells
    Jiang Bo, Liao Yi, Tong Ting-hui
    2011, 15 (27):  5104-5107.  doi: 10.3969/j.issn.1673-8225.2011.27.037
    Abstract ( 105 )   PDF (607KB) ( 307 )   Save

    BACKGROUND: Adipose-derived stem cells inducing epidermal cells are enabled to provide ideal treatment for refractory wounds healing.
    OBJECTIVE: To analyze and sum up the research methods and ideas regarding the adipose derived stem cells in recent 10 years, in a broader attempt to summarize and explore the way how adipose derived stem cells induce epidermal cells.
    METHODS: A computer-based retrieval of VIP Periodical Full-text Database and Wanfang database from January 2001 to October 2010 was performed, with the keywords of ADSCs and adipose derived stem cells in English and Chinese. Articles related with the adipose stem cells tissue engineering were included. Those of irrelevant purpose and repetitive content were ruled out. Finally 26 literatures were summarized.
    RESULTS AND CONCLUSION: As a kind of seed cells available, adipose derived stem cells could directionally induce and differentiate to epidermal cells under some conditions, and improve the ability to induce differentiation and proliferation, thus achieving the goals of clinical usage. Adipose derived stem cells are characterized by abundant sources, easy gain, multi-directional differentiation potentials, good compatibility and small injury to patients, which make it surpass other mesenchymal stem cells. However, adipose derived stem cells manifest infinite proliferation like tumor cells in nonimmune transplanting receptors. The security after transplantation should be observed on suitable animal models in a long term before clinical trial. Moreover, there’s no secure and stable way to cultivate and induce adipose derived stem cells effectively, and how to maintain the quality of cells stable in the process of the abstracting and producing adipose derived stem cells remains further researches.

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    Isolation, cultivation and identification of bone marrow mesenchymal stem cells
    Hu Bin, Liu Xiao-hua, Zhao Lin
    2011, 15 (27):  5108-5111.  doi: 10.3969/j.issn.1673-8225.2011.27.038
    Abstract ( 123 )   PDF (601KB) ( 1024 )   Save

    BACKGROUND: Bone marrow mesenchymal stem cells (BMMSCs) are currently a hot subject of research in many fields such as tissue engineering, cells transplantation and gene therapy.
    OBJECTIVE: To review the biological property, isolation, cultivation and clinical application of BMMSCs.
    METHODS: We had retrieved 30 relevant articles from CNKI and PubMed databases with the key words of “bone marrow mesenchymal stem cells, isolation, cultivation, identification” in Chinese and English, respectively, between January 1995 to January 2010 respectively.
    RESULTS AND CONCLUSION: BMMSCs are nonhematopoietic stem cells and easy to be harvested and cultured which show varying differentiation and high proliferation potentials. BMMSCs can differentiate into osteoblasts, chondrocytes, lipocytes, myocardial cells, nerve cells and hepatocytes, and have become an important seed cells for tissue engineering.

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    Application of neural stem cell transplantation to brain injury therapy
    Chen Lan, Li Mei
    2011, 15 (27):  5112-5114.  doi: 10.3969/j.issn.1673-8225.2011.27.039
    Abstract ( 111 )   PDF (462KB) ( 371 )   Save

    BACKGROUND: Neural stem cells (NSCs), which have the potential of differentiating into neurons and various glial cells, have been isolated from corpus striatum of adult rat brain.
    OBJECTIVE: To summarize the effect and perspective of NSC transplantation in treatment of brain injury.
    METHODS: EMbase (1980-01/2011-04), Medline (1966-01/2011-04), Chinese BioMedical Literature Database (1978/2011-04) and China National Knowledge Infrastructure were retrieved for relevant articles. The key words were “neural stem cells, brain injury, stroke, cerebral infarction”, and finally 12 articles were included.
    RESULTS AND CONCLUSION: Results of animal study demonstrated that NSC transplantation could improve neural function and significantly decrease inflammatory reaction in the brain tissues. Silencing NgR gene, GDNF gene modification and combined transplantation of brain-derived neurotrophic factor could recover neural function to a greater degree. Clinical trials found that NSC transplantation could improve sequela after stroke to some degrees. These suggest that NSC transplantation obtained obvious outcomes, and could be futher utilized in clinic and for studying its clinical outcomes.

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    Neural stem cell gene therapy for exercise-induced spinal cord injury
    Liu Li-xia, Wang Yong-cheng
    2011, 15 (27):  5115-5118.  doi: 10.3969/j.issn.1673-8225.2011.27.040
    Abstract ( 92 )   PDF (603KB) ( 265 )   Save

    BACKGROUND: The neural stem cell gene therapy proposed for sports rehabilitation and treatment of spinal cord injury provides a broad application prospects and challenges.
    OBJECTIVE: To review proliferation and differentiation of neural stem cells as well as neural stem cells gene therapy effect on exercise-induced spinal cord injury.
    METHODS: Medline, VIP, and CNKI databases (1991-01/2010-12) were retrieved for articles about neural stem cell gene therapy for exercise-induced spinal cord injury. The keywords were “neural stem cells, gene therapy, exercise spinal cord injury, gene modification, gene transfection” in English, and “neural stem cells, spinal cord injury, gene therapy” in Chinese. Repetitive and old papers were excluded, and the other papers were organized and analyzed using induction and deduction methods.
    RESULTS AND CONCLUSION: Through modification of neurotrophic factors, proliferation, differentiation and transplantation, the neural stem cell gene therapy can replace necrotic and apoptotic nerve cells in the damaged area and a large number of neurotrophic factors were secreted to improve the local micro-environment for the reconstruction of neural pathways, such as the proliferation of new neurons to promote exercise-induced spinal cord injury. Meanwhile, the neural stem cell gene therapy applied to exercise-induced spinal cord injury also faces with enormous challenges, including whether the neural stem cell gene therapy is mature, high-stable transgenic expression, and other relevant problems, which still need basic research and clinical trials to be addressed.

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    Stem cells and nerve guide conduits for repair of nerve defects
    Wang Su-ping, Wang Zi-han, Peng Dao-yong, Wang Hong, Li Shu-min
    2011, 15 (27):  5119-5122.  doi: 10.3969/j.issn.1673-8225.2011.27.041
    Abstract ( 72 )   PDF (612KB) ( 596 )   Save

    BACKGROUND: Development of tissue engineering can realize the repair of nerve defects. Combination of stem cells and nerve guide conduit scaffold is the core to construct tissue-engineered nerves.
    OBJECTIVE: To investigate how to better repair nerve defects based on tissue-engineering application of stem cells and construction of nerve conduit scaffolds with good biocompatibility.
    METHODS: CNKI and Medline databases were searched for articles addressing stem cells from different sources and nerve conduit scaffolds for repair of nerve defects published from 1996-01 to 2011-01. The keywords were “stem cells, nerve damage, repair, nerve guide conduit, nerve scaffold materials” in Chinese and “stem cells, nerve damage, repair, nerve guide conduit material, scaffold materials, nerve tissue engineering” in English. Repetitive studies or Metal analysis were excluded, and finally 30 articles were included.
    RESULTS AND CONCLUSION: The transplanted neural stem cell can survive, proliferate and migrate in the nervous system, and can be differentiated into corresponding cells at different regions, which brings a new hope for nerve repair. In addition, with the development of biomaterials, nerve conduit materials have also made excellent results in the repair of nerve defects, and have a good prospect. Neural stem cells combined with biodegradable nerve conduit materials are expected to better meet the requirements of nerve scaffolds to achieve the purpose of nerve repair and reconstruction.

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    HLA-identical sibling allogeneic peripheral blood stem cell transplantation in the treatment of acute leukemia
    Chen Bo, Wang Zhi-guo, Zhang Hao, Xiao Liang, Fan Yan-ling, Xia Guo-qiang, Qiu Lin, Zhan Zhao-min, Zhang Bo-long, Ma Jun
    2011, 15 (27):  5123-5126.  doi: 10.3969/j.issn.1673-8225.2011.27.042
    Abstract ( 122 )   PDF (493KB) ( 555 )   Save

    BACKGROUND: HLA-identical sibling allogeneic peripheral blood hematopoietic stem cell transplantation (allo-PBSCT) is an effective treatment method for acute leukemia.
    OBJECTIVE: To assess the clinical efficacy and complications of HLA-identical sibling allo-PBSCT for acute leukemia.
    METHODS: A total of 25 patients with acute leukemia received HLA-identical sibling allo-PBSCT. All cases included 20 cases with acute myeloid leukemia and 5 cases with acute lymphocytic leukemia. Conditioning regimen consisted of busulphan and cyclophosphamide or cyclophosphamide and total body irradiation. Mycophenolate mofetil in combination with cyclosporine and methotrexate was used to prevent graft-versus-host disease.
    RESULTS AND CONCLUSION: Hematopoietic reconstitution was observed in all patients during the follow-ups of 2-80 months. The time of neutrophil count ≥0.5×109/L and platelet ≥20×109/L was at day 12.84 (ranged 10-18 days) and day 20.32 (ranges 10-37 days), respectively. The main complications included 12 cases of sepsis, 9 cytomegalovirus infections, 3 herpes zoster virus infections, 10 acute graft-versus-host disease, 11 chronic graft-versus-host disease and 4 hemorrhagic cystitis. After follow-ups, 17 patients (68%) were in disease-free survival and 8 cases died. HLA-identical sibling allo-PBSCT as a treatment for acute leukemia is safe and efficient.

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    Lacrimal film recovery following autologous corneal limbus stem cells transplantation for treatment of primary and recurrent pterygium
    Jin Ji, Xu Guo-xu, Zhang Ji, Wei Xiao-hong, Bu Shu-yang, Tang Hua, Ji Xiao-yan
    2011, 15 (27):  5127-5130.  doi: 10.3969/j.issn.1673-8225.2011.27.043
    Abstract ( 97 )   PDF (630KB) ( 365 )   Save

    BACKGROUND: Previous studies mainly focus on influence of different surgical methods on postoperative lacrimal film recovery.
    OBJECTIVE: To investigate the effect of one surgery, pterygium excision and autologous corneal limbus stem cells transplantation, on lacrimal film recovery between primary and recurrent pterygium.
    METHODS: A total of 32 cases (38 eyes) of primary pterygium and 28 cases (35 eyes) of recurrent pterygium were selected and all underwent pterygium excision and autologous corneal limbus stem cells transplantation. Questionnaire on dry eye, Schirmer I test and break-up time were performed before, one week and one month after operation.
    RESULTS AND CONCLUSION: One week after operation, both groups appeared dryness and shortened break-up time, which was more serious in recurrent pterygium group (P < 0.05); there was no significant difference in Schirmer I test between two groups. One month after operation only recurrent pterygium group appeared dryness and shortened break-up time compared with primary pterygium group, which was nearly recovered (P < 0.05). Results showed that the recovery of tear stability and lacrimal secretion was poorer in recurrent pterygium than in primary pterygium, which partly explains high recurrence rate of recurrent pterygium.

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