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    05 November 2011, Volume 15 Issue 45 Previous Issue    Next Issue
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    Multipotent differentiation status of rat bone marrow mesenchymal stem cells in vitro after shear stress loading
    Liu Lin, Yang Si-yuan, Hu Xuan-yi, Lin Ke, Shi Ying-kang
    2011, 15 (45):  8361-8365.  doi: 10.3969/j.issn.1673-8225.2011.45.001
    Abstract ( 288 )   PDF (1652KB) ( 317 )   Save

    BACKGROUND: The number of mesenchymal stem cells in the bone marrow of adult animals is little.
    OBJECTIVE: To investigate whether shear stress could modify the abilities of growth, amplification and multi-potent differentiation of bone marrow mesenchymal stem cells or not.
    METHODS: SD rat bone marrow mesenchymal stem cells were isolated, cultured and amplified in vitro by Percoll density gradient centrifugation and adherent culture. 1 Pa shear stress was loaded on primary passage mesenchymal stem cells with a flow chamber system for osteogenic and adipogenic differentiation.
    RESULTS AND CONCLUSION: The primary cells were mostly spindle-like in shape, like the fibroblast cells, and formatted clones. After the cells were loaded with shear stress and then passaged, they grew faster and bigger, and had the same morphologic characters similar as primary mesenchymal stem cells. The growth curves showed the growth regularity of all passage cells was similar, the laser scanning confocal microscope showed the CD41 and CD90 were positive, CD31 and CD45 were negative. After the cells were induced for 14 days, the results of Von Kossa strain and oil red O strain were both positive. The abilities of growth, amplification and multi-potent differentiation of bone marrow mesenchymal stem cells maintained after shear stress loading.

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    Effect of hydrostatic compressive loading on the cytoskeletal structure of human bone marrow mesenchymal stem cells
    He Chuan, Liang Jing, Deng Lian-fu, Yang Qing-ming
    2011, 15 (45):  8366-8370.  doi: 10.3969/j.issn.1673-8225.2011.45.002
    Abstract ( 329 )   PDF (1550KB) ( 376 )   Save

    BACKGROUND: Although little is known about the molecular mechanisms by which mechanical signals regulate mesenchymal stem cells (MSCs) differentiation, cytoskeleton may play an important role in procedure of intracellular mechanical signal delivering.
    OBJECTIVE: To investigate the change of the spatial structure of filamentous actin (F-actin), a cytoskeleton protein, under the continuous hydrostatic pressure and the effects of ERK1/2 signaling pathway or integrin α2β1 block on the above-mentioned process.
    METHODS: In vitro cultured hBMSCs were incubated under continuous pressure of 40 or 80 kPa for 1 or 4 hours by hydraulic pressure controlled cellular strain unit, with or without blocking the ERK1/2 signaling pathway by 10 mmol/L U0126 or by 10 mg/L anti-integrin α2β1 antibody.
    RESULTS AND CONCLUSION: The actin filaments of the strained BMSCs were more flimsy and tenuous than untreated osteoblasts and unlike the normal distribution of bundles or membrane-like of the control group, and they were arranged without direction. But after stained for 4 hours cells showed an arrangement more near the unstained cells than after stained for 1 hour. The U0126 interrupted the rearrangement phenomenon of BMSCs under hydraulic pressure more severely than the anti-integrin α2β1 antibody did. BMSCs under hydrostatic compressive loading lead to cytoskeletal reorganization and rearrangement; The ERK1/2 signaling pathway plays an important role in the process.

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    Effect of bone marrow mesenchymal stem cells on down-regulation of Toll-like receptor 8 and Toll-like receptor 9 in spleen mononuclear cells in collagen-induced arthritis mice
    Mao Fei, Qian Hui, Zhu Wei, Yan Yong-min, Gao Shuo, Xu Wen-rong
    2011, 15 (45):  8371-8375.  doi: 10.3969/j.issn.1673-8225.2011.45.003
    Abstract ( 365 )   PDF (706KB) ( 359 )   Save

    BACKGROUND: Mesenchymal stem cells (MSCs) can attenuate the symptoms of collagen-induced arthritis (CIA) mice but the mechanism of which is not clear.
    OBJECTIVE: To explore the effect of MSCs on the expression of Toll-like receptor 8 (TLR8), Toll-like receptor 9 (TLR9) and so on in spleen mononuclear cells in CIA mice.
    METHODS: DBA/1J mice were randomly divided into sham-operation group, positive control group and test group. Chicken Ⅱ collagen was used to establish the model of CIA in mice. Rat MSCs were administered into the test group through intravenous injection.
    RESULTS AND CONCLUSION: The joint diameter of the test mice decreased obviously compared with that of positive control group. Severe inflammation was detected in the positive group mice by histological analysis, which was not seen in the test group and negative group. The expression levels of TLR8, TLR9 and interleukin-1β in spleen mononuclear cells from the test group were decreased compared with those from the positive group which were higher than that from the negative group (P < 0.01, P < 0.05). Statistical analysis showed that there was no correlation between the expression of TLR8 and TLR9 in the positive control group and test group (P > 0.05). The expression of TLR8 and TLR9 in spleen mononuclear cells from CIA mice were decreased by MSCs, and there was no correlation between the expression of TLR8 and TLR9.

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    Biological characteristics of chronic myelogenous leukemia-derived Flk1+CD31-CD34- bone marrow mesenchemal stem cells
    Huang Dong, Li Wei, Liu Yu, Zhu Xi-shan
    2011, 15 (45):  8376-8380.  doi: 10.3969/j.issn.1673-8225.2011.45.004
    Abstract ( 241 )   PDF (1468KB) ( 274 )   Save

    BACKGROUND: We identified a kind of adherent cells from the fetal bone marrow mesenchymal stem cell culture system, which have been confirmed that they can differentiate into hematopoietic and endothelial cells at the single cell level.
    OBJECTIVE: To detect the biological characteristics of bone marrow mesenchymal stem cells so as to provide the direct evidence for treatment of chronic myelogenous leukemia.
    METHODS: We isolated and cultured Flk1+CD31-CD34- cells from chronic myelogenous leukemia patients. Firstly, we study the growth pattern and fluorescence-activated cell sorter of the expanded cells. The expression of the BCR/ABL fusion gene was assayed by nested RT-PCR and FISH.
    RESULTS AND CONCLUSION: Bone marrow mesenchymal stem cells from chronic myelogenous leukemia patients gave rise to a population of adherent cells with a fibroblast like morphology and had high expansion potential. Cell cycle analysis revealed most of these cells were in the G0/G1 phases. We also showed that more than 90% of these cells were positive stained by FITC labeled Flk1, CD13, CD29, CD44, and negative stained by FITC labeled CD31, CD34, CD45. We could identify the expression of BCR/ABL fusion gene by nested RT-PCR and FISH. These findings provide the direct evidence that rearrangement of BCR/ABL gene might happen at least, but not restrict to the level of hemangioblastic progenitor cells, which are responsible for BCR/ABL fusion gene seen in both hematopoietic cells and endothelial cells.

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    Treatment of growth plate defects in rabbits with adipose derived mesenchymal stem cells and small intestinal submucosa composites
    Yang Hao, Zhu Xiao-song, Li Shi-he, Wu Di
    2011, 15 (45):  8381-8385.  doi: 10.3969/j.issn.1673-8225.2011.45.005
    Abstract ( 361 )   PDF (1408KB) ( 295 )   Save

    BACKGROUND: Small intestinal submucosa (SIS) has good biocompatibility, associated with high conservation and rapid degradation of its main component collage.
    OBJECTIVE: To observe reparative effect of adipose derived mesenchymal stem cells (ADSCs)-SIS composites induced by chondrogenic medium in vitro on growth plate defects in rabbits.
    METHODS: Thirty-six New Zealand rabbits of 6-8 weeks old were divided into 3 groups randomly, and 50% of medial growth plate in proximal right tibia was excised. The defects of growth plates in blank group were not filled, the defects of growth plates in control group were filled with SIS without cells, and the defects of growth plates in experimental group were filled with ADSCs-SIS composites induced by chondrogenic medium in vitro for 14 days. rabbits of each group were sacrificed at 4, 8 and 16 weeks, leg bones of both sides were taken off, fixed with 10% formalin solution, X ray photographs were taken to measure tibial length and proximal tibial articular surface angle(PTAS angle). Calculated the differences of PTAS angle and length of left and right tibias of each rabbit, and compared the differences. Paraffin slices stained with HE were used to observe reparative effect of ADSCs-SIS composites on growth plate cartilage.
    RESULTS AND CONCLUSION: Comparison of X ray photograph measurement among 3 groups showed that 16 weeks after operation, proximal tibial articular surface (PTAS) angle difference of the blank group was larger than that of the control group (P < 0.05) and that of the experimental group (P < 0.05), and PTAS angle difference of the control group was larger than that of the experimental group (P < 0.05). Tibial length difference of the blank group was larger than that of the control group (P < 0.05) and that of the experimental group (P < 0.05), and tibial length difference of the control group was larger than that of the experimental group (P < 0.05). Paraffin slices stained with hematoxylin-eosin showed that, 16 weeks after operation, bone bridges could be seen in growth plates of the blank group and control group, and cartilages rearranged like column in the medial half of growth plates in the experimental group. ADSCs-SIS composites induced by chondrogenic medium in vitro could prevent angular deformity and length discrepancy of the tibia effectively after being implanted into medial growth plate defects of the proximal tibia, and could repair cartilage of growth plates.

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    Bone morphogenetic protein-2 combined with adipose derived stem cells for treatment of avascular necrosis of the femoral head in rabbits
    Qi Xin-wen, Wang Zhao-jie, Chen Jun-ping, Zhao Jun-yan, An Rong-ze
    2011, 15 (45):  8386-8390.  doi: 10.3969/j.issn.1673-8225.2011.45.006
    Abstract ( 280 )   PDF (1597KB) ( 341 )   Save

    BACKGROUND: Adipose derived stem cells (ADSCs) and bone morphogenetic protein-2 (BMP-2) have a strong osteogenic capability that is important for the repair of avascular necrosis of the femoral head.
    OBJECTIVE: To observe the combined effects of ADSCs and BMP-2 on avascular necrosis of the femoral head.
    METHODS: The avascular femoral head necrosis models were established in 48 rabbits using liquid nitrogen. The rabbits were divided into control group, core decompression group, ADSCs group and BMP-2+ADSCs group randomly. 
    RESULTS AND CONCLUSION: Tissue repair of femoral head necrosis in ADSCs group and BMP-2+ADSCs group was vigorous. There were more newly formed trabeculae, which were strengthened. X-ray showed no obvious cystic degeneration and collapse of the femoral head. The growth of trabeculae and bone marrow in BMP-2+ADSCs group was more vigorous than that in ADSCs group at 8 weeks. It is indicated that BMP-2 combined with ADSCs have a stronger repairable ability in necrosis of the femoral head necrosisl.

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    Chondrogenic differentiation of rabbit adipose-derived stem cells in culture medium containing transforming factors and transferrin
    Yang Guo-qing, Wang Zhao-jie, An Rong-ze, Zhao Jun-yan, Qi Xin-wen
    2011, 15 (45):  8391-8394.  doi: 10.3969/j.issn.1673-8225.2011.45.007
    Abstract ( 241 )   PDF (1203KB) ( 320 )   Save

    BACKGROUND: The choice of seed cells is a key factor to the cartilage tissue engineering.
    OBJECTIVE: To explore the chondrogenic potential of adipose-derived stem cells (ADSCs) in culture medium containing transforming factors and transferring.
    METHODS: ADSCs were obtained from the subcutaneous adipose tissue of 6-month-old New Zealand white rabbits’ neck back by mechanical digestion and enzyme digestion, and then cultured and amplified in vitro. The adhesion and growth of cells were observed using inverted phase contrast microscope. Two weeks after the cells were cultured in chondrogenic medium, collagen type Ⅱ expression was detected by immunohistochemistry staining.
    RESULTS AND CONCLUSION: The primary stem cells isolated from adipose tissue adhered on the plate in 24 hours, and reached 90% confluence in single layers after 96 hours. The cartilage nodules were observed at 7 days after ADSCs were cultured under chondrogenic medium, while collagen type Ⅱ was positive 14 days later. ADSCs of rabbits can express chondrogenic phenotype when they were cultured in chondrogenic medium, which proves the ADSCs can be one of the options for cartilage tissue engineering.

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    The growth of nasopharyngeal cancer stem cell SP18 affected by carboxy terminal activating region-3 of the Epstein-Barr virus encoded latent membrane protein 1
    Quan Sheng, Zhuang Ying-zhi, Zhang Zhi-wei, Liu Zhong-yuan, Jiang Hao, Zhao Qiang, Zhu Jian-si, Dong Lin
    2011, 15 (45):  8395-8398.  doi: 10.3969/j.issn.1673-8225.2011.45.008
    Abstract ( 283 )   PDF (1063KB) ( 282 )   Save

    BACKGROUND: Carboxy terminal activating region-3 of the Epstein-Barr virus encoded latent membrane protein 1 (LMP1-CTAR3) has been constructed in the previous studies. CTAR3 plays an important role in LMP1.
    OBJECTIVE: To observe the effect of LMP1-CTAR3 on the growth of nasopharyngeal cancer stem cell SP18.
    METHODS: We adopted the method of retroviruses infection and established the nasopharyngeal cancer stem cell SP18 of stable expression LMP1 and LMP1△232-351. Then, we made use of cell growth curve, plate clone formation and soft agar colony experiment to observe the growth of nasopharyngeal cancer stem cell SP18 affected by LMP1△232-351. Meanwhile, we detected the cycle of SP18-LMP1△232-351 cell by flow cytometry and calculated cellular proliferation index. In addition, Western-blot detection was used to determine phosphorylation JAK3 protein.
    RESULTS AND CONCLUSION: Compared with SP18-LMP1 cells, the growth velocity and proliferation index of SP18-LMP1△232-351 cells obviously decreased (P < 0.01). The expression of phosphorylation JAK3 protein in SP18-LMP1△232-351 cells was lower than that in SP18-LMP1 cells. LMP1-CTAR3 probably affected the expression of phosphorylation JAK3 protein in SP18 to decrease cellular proliferation index and reduce the ability of cell proliferation promoted by LMP1.

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    Immuno-modulatory effect of cancer stem cells from chronic myeloid leukemia patients
    Li Ji-hong, Huang Ai-ben, Ma Ying-min
    2011, 15 (45):  8399-8403.  doi: 10.3969/j.issn.1673-8225.2011.45.009
    Abstract ( 198 )   PDF (527KB) ( 335 )   Save

    BACKGROUND: Studies have suggested that mesenchymal stem cells may be immune protection sites consisting of the bone marrow micro-environment. As chronic myeloid leukemia hematopoietic microenvironment abnormalities and immune abnormalities exist, mesenchymal stem cells in chronic myelogenous leukemia presumably play an important role in the pathological process.
    OBJECTIVE: To observe the immunological characteristics and the existence of immune dysfunction of bone marrow-derived cancer stem cells from chronic myeloid leukemia in comparison with normal mesenchymal stem cells.
    METHODS: Bone marrow mesenchymal stem cells were separated from the normal subjects and patients with chronic myeloid leukemia to detect the effect on T cell cycle, activation, inhibition and proliferation.
    RESULTS AND CONCLUSION: There were no differences between mesenchymal stem cell from chronic myeloid leukemia patients and normal volunteers in cell morphology and phenotype, but the ability of mesenchymal stem cells from chronic myelogenous leukemia patients was decreased in inhibiting T cell proliferation, T cell cycle and activation and increased in T cell apoptosis. All these indicate that mesenchymal stem cells from chronic myelogenous leukemia patients have obvious immune function defects, which are not a preferred choice for autologous mesenchymal stem cell transplantation. Allogeneic mesenchymal stem cell transplantation is the best method to be used in patients with myelodysplastic syndrome.

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    Proliferation characteristics of tumor stem cells in MCF7 cell line
    Huang Ming-wei, Lu Yun-fei
    2011, 15 (45):  8404-8407.  doi: 10.3969/j.issn.1673-8225.2011.45.010
    Abstract ( 461 )   PDF (745KB) ( 279 )   Save

    BACKGROUND: The hypothesis of tumor stem cells posited that tumor stem cells are the root of tumor proliferation constantly and closely related to tumor biological behaviors such as infiltration, metastasis and drug-resistant.
    OBJECTIVE: To investigate the proliferation characteristics of tumor stem cells in MCF7 cell line in vitro by studying the tumorigenic-colony forming rate at single cell level.
    METHODS: Tumor stem cells proportion in MCF7 cell line was detected at series timing after passaged culture by single-cell-transplanting and tumorigenic-colony forming assay. The proportion of the CD44+/CD24-/low subset was detected by flow cytometry at the same time.
    RESULTS AND CONCLUSION: The proportion of tumor stem cells and the CD44+/CD24-/low subset in MCF7cell line both varied regularly after passaged culture. But the variation of CD44+/CD24-/low (from 36.84% to 81.95%) subset was more drastic than that of tumor stem cells proportion,which only fluctuated in a limited range from 38.54% to 47.39%. The proportion of tumor stem cells was steady in MCF7 cell line after passaged culture, owing to the property of tumor stem cells to modulate and balance the proportion by itself. CD44+/CD24-/low subset neither represented nor enriched tumor stem cells subset in MCF7 cell line.  

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    Immunological characteristics of human umbilical cord derived mesenchymal stem cells transplanted in vivo and vitro
    Ye Xiang-yang, Xu Yan, Bi Wei-wei, Guo Li-bin, Li Xiang-jun, Liu Jian-guo
    2011, 15 (45):  8408-8412.  doi: 10.3969/j.issn.1673-8225.2011.45.011
    Abstract ( 340 )   PDF (727KB) ( 363 )   Save

    BACKGROUND: Human umbilical cord derived mesenchymal stem cells (HUC-MSCs) have been confirmed to have the characteristics of immunologic tolerance in vitro, but there are no relevant allogenic research in vivo. The results and mechanism are lack of consistency.
    OBJECTIVE: To cultivate HUC-MSCs and research the immunological characteristics of implanted HUC-MSCs in vivo and in vitro.
    METHODS: HUC-MSCs were obtained by using tissue adhesion method. Mixed-leukocyte reaction (MLR) was performed to evaluate immunologic tolerance in vitro, flow cytometry applied to detect the changes of CD4 and CD8 expression as well as ratio of CD4 to CD8, and ELISA used to detect interleukin 2 (IL-2), IL-10, γ-interferon (IFN-γ) levels.
    RESULTS AND CONCLUSION: MLR results showed a similar trend in the concentration changes of cytokines: the level of IL-10 slightly increased after MLR reaction (P < 0.05), while the level of IFN-γ decreased (P < 0.05). The ratio of CD4+/CD8+ in T cell subsets was decreased to a slight extent after cell transplantation, indicating that HUC-MSCs possessed the characteristics of allogeneic immunological tolerance and immunoloregulation effect.

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    Effects of multi-intravenous transplantation of human cord blood mononuclear cells on the remodeling of cardiac collagen after myocardial infarction in rabbits
    Li Wen-bin, Yu Guo-long, Yuan Chun-ju, Yang Tian-lun
    2011, 15 (45):  8413-8417.  doi: 10.3969/j.issn.1673-8225.2011.45.012
    Abstract ( 263 )   PDF (1600KB) ( 320 )   Save

    BACKGROUND: In previous studies, the treatment of myocardial infarction by using stem cell transplantation was done via single intravenous or coronary injection transplantation.
    OBJECTIVE: To investigate the effects of multi-intravenous transplantation of human cord blood mononuclear cells (HCBMCs) on the remodeling of cardiac collagen and heart function after myocardial infarction in rabbits.
    METHODS: Forty-five Chinese rabbits underwent ligation of the left anterior coronary artery for the preparation of myocardial infarction models. They were randomly divided into three groups. ①Multi-transplantation group: They were intravenously injected with HCBMCs labeled with bromodexyuridine (BrdU) and normal saline at 7, 9, 11 and 13 days post-operation. ②Single cell transplantation group: They were intravenously injected with HCBMCs labeled with BrdU at 7 days post-operation and normal saline at 9, 11, and 13 days post-operation. ③Control group: They were intravenously injected with normal saline at 7, 9, 11 and 13 days post-operation. In addition, five Chinese rabbits acted as the sham operation group.
    RESULTS AND CONCLUSION: Compared with the control group, left ventricular fractional shortening (LVFS) and left ventricular ejection fraction (LVEF) were improved significantly in the multi-transplantation group and single cell transplantation group (P < 0.05); while LVFS and LVEF were improved more significantly in the multi-transplantation group than in the single-transplantation group (P < 0.05); immunohistochemistry results demonstrated that BrdU positive cells were found in the peri-myocardial infarction area in the both transplanted groups at 2 and 4 weeks after the operation. Moreover, the number of BrdU positive cells in the multi-transplantation group was larger than that in the single-transplanted group. Masson's trichrome staining showed that compared with the sham operation group, the density of collagen fibers in the control group was significantly increased, and the collagen fibers were fused partially and arranged irregularly. Compared with the control group, the collagen and collagen fibers in both transplanted groups were decreased significantly, and the collagen fibers arranged more regularly after the operation. The multi-intravenous transplantation of HCBMCs for myocardial infarction is superior in improving cardiac function and inhibiting myocardial collagen remodeling, compared to single intravenously transplanted HCBMCs.

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    Angelica sinensis (oliv.) diels and lycium chinense mill preparations induce the differentiation of cord blood mononuclear cells into hepatocyts: Expression of human albumen
    Fu Jing-li, Zeng Yan, Long Ze-ling, Tang Xiao-peng
    2011, 15 (45):  8418-8423.  doi: 10.3969/j.issn.1673-8225.2011.45.013
    Abstract ( 246 )   PDF (1708KB) ( 300 )   Save

    BACKGROUND: Some traditional Chinese medicine can promote the differentiation and growth of human hematopoietic stem cells.
    OBJECTIVE: To observe the promotion effect of angelica sinensis (oliv.) diels and lycium chinense mill preparation for the differentiation of human umbilical cord blood stem cells (HUCBSCs) into hepatocytes in vitro and in vivo.
    METHODS: HUCBSCs were separated and cultured in different doses of angelica sinensis (oliv.) diels and lycium chinense mill preparation to screen the suitable dosage for HUCBSCs growth. Albumen mRNA and alpha fetoprotein mRNA expression were detected by RT-PCR. The liver failure models of rats were established after D-aminogalactose was injected intraperitoneally. The survival rats with acute hepatic injury were randomly divided into eight groups to detect the changes of liver function.
    RESULTS AND CONCLUSION: 90 mg/L angelica sinensis (oliv.) diels and 40 mg/L lycium chinense mill preparation was suitable for HUCBSCs proliferation and differentiation. Both angelica sinensis(oliv.) diels and lycium chinense mill preparation could promote and speed up the differentiation of HUCBSCs into hepatocytes, and the former one was superior to the latter one. However, there was no synergistic effect. The difference between groups treated with/without cyclophosphamide was not obvious.

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    Human umbilical cord derived mesenchymal stem cell transplantation for rat traumatic brain injury
    Yuan Yuan, Yang Shu-yuan, Zhang Jian-ning
    2011, 15 (45):  8424-8428.  doi: 10.3969/j.issn.1673-8225.2011.45.014
    Abstract ( 213 )   PDF (1895KB) ( 422 )   Save

    BACKGROUND: There are rare reports about umbilical cord derived mesenchymal stem cells (UCMSCs) transplantation in the treatment of brain injury.
    OBJECTIVE: To investigate the effects and mechanism of UCMSCs transplantation on the repair of rat brain fluid percussion injury.
    METHODS: UCMSCs were separated from new-born umbilical cord and cultured in vitro, labeled with BrdU, and transplanted into rat brain 24 hours after fluid percussion injury. There were four groups: UCMSCs transplantation group, in situ UCMSCs transplantation; control group, injected with the same volume of DMEN/F12 medium; model group, without treatment; sham-injury group, no fluid percussion injury was made.
    RESULTS AND CONCLUSION: Significant recovery of behavior was found in UCMSCs-treated rats at 1-3 weeks after transplantation. Immunohistochemical analysis showed that a small number of transplanted cells expressed neuron-specific enolase and glial fibrillary acidic protein. Compared with the control group, the expression of vascular endothelial growth factors increased in the injured region and the number of apoptotic cells decreased in the UCMSCs transplantation group. These findings show that UCMSCs transplantation can promote the early function recovery following brain fluid percussion injury through stimulating the secretion of vascular endothelial growth factors, increasing the number of microvessels in the injured region, and inhibiting cell apoptosis.

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    Optimization of separation methods and culture system of chicken embryonic stem cells in vitro
    Zhang Man-yu, Chen Zhi-cheng, Ji Hui-qin, Chen Sheng-feng, Liu Ben-jie, Deng Xian-bo, Wang Bing-yun, Yuan Li, Jiang Qing-yan
    2011, 15 (45):  8429-8433.  doi: 10.3969/j.issn.1673-8225.2011.45.015
    Abstract ( 340 )   PDF (1280KB) ( 686 )   Save

    BACKGROUND: Embryonic stem cells are undifferentiated permanent cell line derived from inner cell mass cells and primordial germ cells of animal’s early embryos. Chicken embryonic stem cells are derived from the blastodermal of a X-stage embryo.
    OBJECTIVE: To optim the separation method and in vitro cultural system of chicken embryonic stem cells.
    METHODS: The X-stage chicken embryos were isolated by using a small square of ?lter paper with a hole punched in the center, and the blastodermal cells were isolated by using the hair loop. STO cells were used to make feeder layer; at the same time, BRL-CM and cytokine were also used for chicken embryonic stem cells in vitro cultural system.
    RESULTS AND CONCLUSION: The filter paper loop and the hair loop could obtain complete the blastoderm, and the successful percentage was 75%-85%. The colony formation rate was about 50%. After culture in the BRL-CM + feeder layer + cytokine culture system, the passage of CES cells is the seventh generation; BRL-CM + feeder layer + cytokines, cultured chicken embryonic stem cells could passage to the 25th generation. Isolated chicken embryonic stem cells were in an undifferentiated state detected by alkaline phosphatase staining and SSEA-1 staining. The findings indicate that this experiment not only optimized the isolation method of chicken embryonic stem cells to obtain complete and pure embryos, but also further improved the in vitro culture system of chicken embryonic stem cells.

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    Comparison of pre-injury and improved passage methods for Schwann cells cultured in vitro
    Yang Jun, Qin Jian-qiang, Pei Guo-xian, Guo Xin-hui, Ye Han-shen, Chen Da-jun, Hong Jia-jin, Cai Wei-bin
    2011, 15 (45):  8434-8438.  doi: 10.3969/j.issn.1673-8225.2011.45.016
    Abstract ( 274 )   PDF (491KB) ( 285 )   Save

    BACKGROUND: Tissue engineering methods to construct nerve bridge graft for repairing nerve injury requires massive purified Schwann cells cultured in vitro.
    OBJECTIVE: To compare the purity and quality of Schwann cells obtained with the pre-injury method and improved passage method.
    METHODS: (1) Pre-injury method: Sciatic nerve of Sprague-Dawley neonatal rats was pre-injured for 3 days and removed, the epineurium was isolated and digested with trypsin and collagenase. Schwann cells were cultured in the culture medium after fibroblasts were eliminated with differential adhesion method. (2) Improved passage method: Sciatic nerve was directly removed from Sprague-Dawley neonatal rats and the epineurium was isolated. Double-enzyme digestion and single-enzyme digestion methods were adopted to primarily culture Schwann cells for 5-7 days. Schwann cells were purified with a single enzyme rapid digestion and centrifugation.
    RESULTS AND CONCLUSION: Both pre-injury and improved passage methods obtained 95% purity of Schwann cells cultured in vitro, with no significant difference (P > 0.05). The resultant Schwann cells obtained by two methods showed normal morphology, high quantity, high purity and productive growth. These experimental findings imply that both pre-injury and improved passage methods are ideal approaches for in vitro culture of Schwann cells with high quality and high purity.

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    Glial-derived neurotrophic factor induces the in vitro differentiation of mesencephalic neural stem cells into dopaminergic neurons under normoxic and hypoxic conditions
    Luo Te-jian, Ding Ji-gu
    2011, 15 (45):  8439-8442.  doi: 10.3969/j.issn.1673-8225.2011.45.017
    Abstract ( 238 )   PDF (1158KB) ( 252 )   Save

    BACKGROUND: Directed differentiation and proliferation of nerve stem cells are regulated by their own genes and external signals.
    OBJECTIVE: To observe the differentiation of mesencephalic neural stem cells into dopaminergic neurons under normoxic and hypoxic conditions induced by glial-derived neurotrophic factor (GDNF).
    METHODS: Under aseptic conditions, we isolated mesencephalic tissues from E12 mouse embryos. Single cell suspension was prepared by pancreas enzyme digestion and mechanical pipetting, and were cultured and proliferated in serum-free medium. Nestin immunocytochemistry staining was used to identify nerve stem cells. Purified nerve stem cells differentiated in serum medium. Neuron-specific enolase and glial fibrillary acidic protein immunocytochemistry staining methods were performed to identify neurons and astrocytes, respectively. All the cells were divided into normoxia group, normoxia+GDNF group, hypoxia group, hypoxia+GDNF group, and then cultured in serum medium.
    RESULTS AND CONCLUSION: Under the hypoxia condition, mesencephalic neural stem cells had a higher differentiated rate than that in the normoxia group. The number of differentiated cells in the hypoxia+GDNF group was higher than that of the other groups, and the differentiated cells had a mature phenotype. It is indicated that under the hypoxic condition, GDNF can extremely promote the differentiation of nerve stem cells into dopaminergic neurons with good morphology and mature function.

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    Batroxobin influences the orientated differentiation and proliferation of endothelial progenitor cells from human peripheral blood in vitro
    Wu Wei, Sun Xiao-jie, Cui Pei-yuan, Lu Zheng
    2011, 15 (45):  8443-8446.  doi: 10.3969/j.issn.1673-8225.2011.45.018
    Abstract ( 232 )   PDF (1080KB) ( 249 )   Save

    BACKGROUND: In recent years, it has been known that endothelial progenitor cells (EPCs) promote the angiogenesis of the body, but the directed differentiation and proliferation of EPCs limits their efficacy and widespread application.
    OBJECTIVE: To investigate the feasibility of inducing human peripheral blood derived EPCs into endothelial cells in vitro, and to test their phenotype and function.
    METHODS: Mononuclear cells (MNCs) were isolated from the peripheral blood by using Percoll density gradient centrifugation. The cells were then plated on fibronectin-coated culture dishes. After being cultured for 6 days, the attached cells were collected. EPCs were characterized as adherent cells double positive for DiI-LDL-uptake and lectin binding by direct flurescent staining under a laser scanning confocal microscope. The attached cells were cultured and induced by vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) in vitro. The morphological changes of the cells were observed. The cells were enumerated by flow cytometry (FCM) with CD31 monoclonal antibody and vWF monoclonal antibody. The attached cells were stimulated with DF-5201 (final concentration: 0.05, 0.1, 0.2 BU/mL) for the respective time points (6, 12, 24 and 48 hours). Proliferation ability of EPCs was assayed by MTT assay.
    RESULTS AND CONCLUSION: After induced by VEGF and bFGF in vitro, EPCs became endothelial cell like cells and CD31 and vWF were expressed. Incubation of isolated human MNCs with DF-521 dose- and time-dependently increased the number of EPCs. EPCs can differentiate into endothelial cells by the induction of VEGF and bFGF. Incubation of EPCs with DF-521 increased the proliferative ability at different concentration.

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    An exploration of the optimal conditions for isolating umbilical cord blood mononuclear cells by using two-step methods
    Guo Ji-qiang, Liu Ai-bing, Shen Dan
    2011, 15 (45):  8447-8450.  doi: 10.3969/j.issn.1673-8225.2011.45.019
    Abstract ( 322 )   PDF (1280KB) ( 423 )   Save

    BACKGROUND: It has not been deeply reported how to obtain high-purity and high-vigor stem cells as well as the standardized operation plan has not been seen, yet.
    OBJECTIVE: To explore the best condition for isolating human umbilical cord blood mononuclear cells.
    METHODS: Umbilical cord blood red blood cells precipitated by hydroxyethyl starch were observed in different time points (20, 30, 40, 50, 60, 70 minutes). The human umbilical cord blood mononuclear cells were separated in human lymphocyte separating medium (LSM) by using centrifugation method at 800, 700, 600, 500, 400 g/min for 30, 25, and 20 minutes.
    RESULTS AND CONCLUSION: The 6% hydroxyethyl starch precipitation for umbilical cord blood red blood cells was best within 60 minutes. Using the human LSM of (1.077 0±0.000 1) g/mL at 4 ℃, centrifugation at 700 g/min for 30 minutes, and rinsing for 3 times the best conditions to harvest human umbilical cord blood mononuclear cells. Under the above-mentioned conditions, not only higher umbilical cord blood mononuclear cells rate and higher mononuclear cells vigor were obtained, but fewer red blood cells and other cell fragments were seen. The best condition for isolating the human umbilical cord blood mononuclear cells using two steps methods (6% hydroxyethyl starch precipitation and LSM) at the optimal time can improve the recovery rate of human umbilical cord blood stem cells.

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    Expression of Mash-1 in hippocampal neural stem cells after cerebral ischemia/reperfusion injury in rats
    Lü Wei-li, Xing Xue-song, Zhang Ling, Zhang Min
    2011, 15 (45):  8451-8454.  doi: 10.3969/j.issn.1673-8225.2011.45.020
    Abstract ( 361 )   PDF (1046KB) ( 267 )   Save

    BACKGROUND: Mash-1 is expressed during the development of the central nervous system and peripheral nervous system, and plays an important role in neurons and glial cell differentiation.
    OBJECTIVE: To investigate the expression of Mash-1 in the hippocampus after cerebral ischemia/reperfusion in rats.
    METHODS: A novel model of cerebral ischemia/reperfusion was established with the method of middle cerebral artery occlusionin rats. The rats were divided into sham-operation group, and ischemia/reperfusion groups of 3, 7, 14, 21 and 28 days.
    RESULTS AND CONCLUSION: After 3 days, BrdU positive cells in the hippocampus were obviously increased. To the 7th day, BrdU positive cells were more than those at any time. Mash-1 reaction products were increased gradually with the time of cerebral ischemia/reperfusion, reached the peak on day 21, and then gradually decreased. The expression of Mash-1 is in a time-depended manner and corresponds to the proliferation and differentiation of neural stem cells, suggesting that Mash-1 can play the important effect in regulating the neural stem cell differentiation in the late stage.

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    Effect of bone marrow stromal cells on neurotrophic factors of rats with ischemic cerebral infarction
    Bian Ying, Sun Feng, He Zhi-yi
    2011, 15 (45):  8455-8458.  doi: 10.3969/j.issn.1673-8225.2011.45.021
    Abstract ( 234 )   PDF (1033KB) ( 256 )   Save

    BACKGROUND: Bone marrow stromal cells (BMSCs) can differentiate into neurons and astrocytes under the appropriate conditions, and secrete soluble molecules to promote neuronal survival.
    OBJECTIVE: To observe the effect of test the effect of BMSCs on neurotrophic factors and neurologic function of rats with ischemic cerebral infarction.
    METHODS: Rats were subjected to transient middle cerebral artery occlusion and intravenously injected with 3×106 BMSCs (treatment group) and 1 mL normal saline (saline group) at 24 hours after stroke. No administration was done in blank control group.
    RESULTS AND CONCLUSION: Significant recovery of neurological function was found in the treatment group at 7 and 14 days after stroke in comparison with the other two groups (P < 0.05). Nerve growth factor and brain derived neurotrophic factor had a higher expression in the treatment group than the other two groups at different time points (P < 0.05). Intravenous injection of BMSCs can improve the neurologic function of rats with ischemic cerebral infarction and the increase in the expression of nerve growth factor and brain derived neurotrophic factor in the ischemic tissue plays an important role in neurological recovery.

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    Effects of autologous olfactory mucoma combined with beta-aesine sodium on expression of matrix metalloproteinase-2 and matrix metalloproteinase-9 in rats following spinal cord injury 
    Cheng Hua, Liu Zeng-xu, Xu Nian-xiang, Luo Xiao-feng, Yu Qing, Liu Hui-fang, Liu De-ming
    2011, 15 (45):  8459-8462.  doi: 10.3969/j.issn.1673-8225.2011.45.022
    Abstract ( 279 )   PDF (1576KB) ( 270 )   Save

    BACKGROUND: After spinal cord injury, over-expression of metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) contributes to secondary tissue damage of the spinal cord.
    OJECTIVE: To study the influence of autologous olfactory mucoma combined with β-aesine sodium on expression of MMP-2, 9 and the recovery of neural function of injured spinal cord in adult rats.
    METHODS: In this study, healthy Sprague-Dawley rats with T10 spinal cord hemisection were divided into four groups as follows: control group (A), autologous olfactory mucoma transplantation group (B), β-aesine sodium group (C), combination group (D).
    RESULTS AND CONCLUSION: The BBB scales showed that rats in groups B, C and D had more improvement than those in group A at series of phases at 7 and 14 days after operation (P < 0.05), and the BBB score of group D was much higher than that of group B and group C (P < 0.05). The expression of MMP-9 and MMP-2 in injured spinal cord increased significantly at all time points. The number of positive cells in group D was less than that in groups B and C at the corresponding time points (P < 0.05), but there were no statistically significant differences between group B and C (P > 0.05). The method of treating spinal cord injury by autologous olfactory mucosa transplantation combined with β-aesine sodium has good curative effect, and can largely improve hind limbs motor function, which may be related to inhibiting the overexpression of MMP-9 and MMP-2 genes.

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    Intravenous transplantation of bone marrow mesenchymal stem cells in the treatment of spinal cord injury in rats
    Yu Chang-shen,Guan Ya-lin, Wang Shi-min, Xu Xiao-lin, Wang Xin-ping, Yan Xiao-ling, Zhang Xue-qing
    2011, 15 (45):  8463-8468.  doi: 10.3969/j.issn.1673-8225.2011.45.023
    Abstract ( 256 )   PDF (2147KB) ( 279 )   Save

    BACKGROUND: Transplantation of stem cells can rebuild the structure and function of injured central nervous system, and has attracted wide attention in recent years.
    OBJECTIVE: To explore the effects and mechanisms of bone marrow mesenchymal stem cells (BMSCs) transplanted through the vena caudalis on neurological recovery of rats with spinal cord injury.
    METHODS: BMSCs were separated with density gradient centrifugation and adherent screening methods. Forty adult female Wistar rats were used to establish the models of spinal cord injury using aneurysm clips, and then randomized into two groups: control group and BMSCs transplantation group.
    RESULTS AND CONCLUSION: The BMSCs transplantation group showed higher BBB scores than the control group (P < 0.05). Since the 30th day after injury, the motor evoked potential latency and somatosensory evoked potential P1 wave latency of the BMSCs transplantation group were shorter than those of the control group (P < 0.05), and these phenomena continued until the end of experiment. Positive cells could be noted at the sites 1 cm distant from the injured centre of the spinal cord. BMSCs transplantation via the vena caudalis can remarkably promote the recovery of neural function in rats with spinal cord injury, and the mechanism may be related to that transplanted BMSCs can survive, migrate and differentiate into neuron like cells and neuroglia like cells, and can promote the expression of neurotrophic factors.

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    Labeling and tracing bone marrow mesenchymal stem cells with PKH-26 in vivo
    Han Yun, Pang Chao-jian, Lan Ni, Tong Xiao-jie, Shi Wen-jun
    2011, 15 (45):  8469-8473.  doi: 10.3969/j.issn.1673-8225.2011.45.024
    Abstract ( 304 )   PDF (1607KB) ( 955 )   Save

    BACKGROUND: PKH-26 has been successfully applied to label bone marrow mesenchymal stem cells (BMSCs).
    OBJECTIVE: To evaluate the effect of PKH-26 on the labeling and tracing of BMSCs via tracheal transplantation and vein transplantation and to detect the migration of labeled BMSCs into the injured sites.
    METHODS: BMSCs were cultured by adherence method. PKH-26 labeled 3-5 passage BMSCs were injected into the recipient rats via the tail vein. Rats in the control groups were injected with the same amount of PBS.
    RESULTS AND CONCLUSION: After PKH-26 labeling procedure, almost all BMSCs were labeled with red fluorescence under inverted fluorescence microscope, indicating that the labeling method has high sensitivity and efficiency. In vivo tracing showed that red fluorescence was still visible at 8 weeks post-surgery at the recipient and transplanted trachea, with most red fluorescence shown at the anastomotic part. There was basically no red fluorescence visible at the recipient trachea that was further away from the anastomotic site. These indicated that BMSCs can migrate to the impaired trachea after injected via the tail vein. Also, the BMSCs can further migrate from the recipient tracheal edge to the transplanted trachea and finally locate at the implant site. The highly stable PKH-26 red fluorescence in vivo indicated that it can be used in tracing studies that need long-term observation.

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    Effects of multiple injection of bone marrow mesenchymal stem cells modified with heme oxygenase 1 on myocardial remodeling after myocardial infarction
    Zhang Jing, Li Ming-jiang, Zeng Bin
    2011, 15 (45):  8474-8478.  doi: 10.3969/j.issn.1673-8225.2011.45.025
    Abstract ( 302 )   PDF (1271KB) ( 277 )   Save

    BACKGROUND: Studies have shown that over-expression of heme oxygenase 1 (HO-1) has the effect of anti-inflammation. It is unclear whether injection of bone marrow mesenchymal stem cells (BMSCs) modified with heme oxygenase-1 (HO-1-BMSCs) in infarcted myocardium can significantly improve myocardial remodeling by regulating the ratio of matrix metalloproteinase (MMP) to tissue inhibitors of metalloproteinase (TIMP).
    OBJECTIVE: To investigate the effects of transplantation of HO-1-BMSCs on regulating collagens and myocardial remodeling after myocardial infarction.
    METHODS: BMSCs were cultured and amplificated with HO-1 adenovirus (Adv-HO-1) transfection in vitro. Myocardial infarction models in rats were established by ligating the left anterior descending coronary artery. One hour after modeling, HO-1-BMSCs and BMSCs were respectively transplanted into the infarcted myocardium of rats in a manner of multiple injections. The rats in the control group were given phosphate buffer in the same dose.
    RESULTS AND CONCLUSION: Adv-HO-l stably expressed in BMSCs after transfection, while hHO-1-mRNA only expressed in HO-1-BMSCs. The expression of MMP2/9 in the HO-1-BMSCs group was decreased compared with that in the control group (P < 0.05), the reduction in Null- BMSCs was insignificant (P > 0.05). Compared with the control group, the expression of MMP2/3 was significantly increased in the other two groups, especially in the HO-1-BMSCs group (P < 0.05), but MMP1 did not change significantly (P > 0.05). The ratio of TIMP2 to MMP2 in cell transplantation groups was significantly increased, so was the ratio of TIMP3 to MMP9. Collagen was deposition decreased and ventricular was reduced in cell transplantation groups compared with the control group. The results showed that injection of HO-1-BMSCs can normalize the ratio of MMPs/TIMPs, as well as contribute to the revision of myocardial extracelluar remodeling.

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    Isolation of side population cells in leukemia K562 cell lines and the expression of resistance protein and cell cycle in two subpopulations
    Fan Rui-hua, Li Hui-min, Guo Dian-xuan, Gao Yong, Chen Xiao-fei
    2011, 15 (45):  8479-8482.  doi: 10.3969/j.issn.1673-8225.2011.45.026
    Abstract ( 316 )   PDF (540KB) ( 308 )   Save

    BACKGROUND: It is possible that leukemia relapse is related with side population (SP) cells, which can escape cell cyles phase specific chemotherapeutic drugs .
    OBJECTIVE: To isolate and preliminarily identify whether the human chronic myeloid leukemia cell line-K562 contains SP cells or not, and to further research K562 SP cells and study the expression of multidrug resistance proteins and DNA content in two subpopulations.
    METHODS: Flow cytometry with UV excitation light was used to detect the percentage of SP cells in logarithmic growth period K562, which were then sorted by the fluorescence activating cell sorter, and then SP and non-SP subpopulations were collected. The expression of multidrug resistance proteins were examined by flow cytometry technique in two subpopulations. DNA content of two subpopulations was examined by flow cytometry.
    RESULTS AND CONCLUSION: The K562 cell line contained SP cells, and the proportion of SP cells was much lower. Although there were no differences between these two subpopulations in P-gp expression, ABCG2+ cells expression in the SP subpopulation was significant higher than that in the non-SP subpopulation (P < 0.05). The G0/G1 phase cells in the K562 SP subpopulation accounted for about 80% of the total cells. According to the significant differences in the expression of MDR proteins between the SP subpopulation and the non-SP subpopulation, and the majority in a quiescent period, it is possible that leukemia stem cells are enriched in SP cells.

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    Statistical analysis for ambiguous results of HLA-A*02 high-resolution genotyping by using PCR-SSO flow fluorescent bead method
    Zhang Rong-da, Du Juan, Ma Xiao-li, Zhang Bo-wei
    2011, 15 (45):  8483-8486.  doi: 10.3969/j.issn.1673-8225.2011.45.027
    Abstract ( 287 )   PDF (600KB) ( 378 )   Save

    BACKGROUND: Due to the complexity of the HLA typing system, ambiguous situations occur frequently during HLA typing of the donors.
    OBJECTIVE: To statistically analyze the ambiguous ratio and combined allele groups of HLA-A*02 high-resolution genotyping by using PCR-SSO flow fluorescent bead method, and to investigate the method to resolve the ambiguous results of HLA-A*02 high-resolution genotyping and improve the ratio of high-resolution genotyping.
    METHODS: 1100 pieces of HLA genotyping were collected for statistical analysis. We calculated the percentages of those combinations that contained HLA-A*02:01\02:09 ambiguity, given by the software HLA Fusion 2.0; in the other hand, we searched out those alleles which were highly correlated with A*02:09 by comparing these combination percentages with the A*02:09 genetic polymorphism distribution.
    RESULTS AND CONCLUSION: 279 out of 1039 effective samples (279/1039, 26.853%) were found for the results of having A*02:01/02:09 ambiguities that could be categorized into 19 groups in NMDP code. The most frequently groups were DMDC, DYVK, GMDD, GMDE. In another cases, 34 identified as carrying A*02:09 were analyzed appearing that A*02:09 was highly correlated to B*07:02(0.2647), DRB1*01:01(0.2647), DRB1*03:01(0.1176). We selected 38 high risky samples and tested their 4-7 exons, and confirmed by SBT, only 1 sample could be identified as A*0209, while other 241 samples lacked of A*02:09. A reasonable judgment based on statistical analysis and necessary review can effectively simplify the experimental procedures, save time, reduce costs, and increase high-resolution ratio.

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    Immunophenotype of acute lymphoblastic leukemia and detection of CD4+CD25+ regulatory T cells
    Wu Cui-ping, Qin Xi, Wu Cui-yun, Zhu Hong, Zhou Hai-yan
    2011, 15 (45):  8487-8490.  doi: 10.3969/j.issn.1673-8225.2011.45.028
    Abstract ( 296 )   PDF (510KB) ( 308 )   Save

    BACKGROUND: CD4+CD25+ regulatory T cells (Treg) may have a certain regulatory effect on immune response in the pathogenic process of acute lymphoblastic leukemia (ALL).
    OBJECTIVE: To explore the immunophenotype and the changes of Treg in the peripheral blood of patients with ALL.
    METHODS: The immunophenotype and levels of CD4+CD25+Treg in the peripheral blood were detected using flow cytometry in 35 ALL patients in comparison with the health control people.
    RESULTS AND CONCLUSION: There were 22 B-ALL cases and 13 T-ALL cases among 35 ALL patients. CD19 expression of the cases of B-ALL had the highest positive rate (100%); meanwhile, CD7 expression of the cases of T-ALL had the highest positive rate (100%). There were no significant difference between the number of CD4+CD25+ Treg cells in B-ALL and T-ALL patients (P > 0.05), but there were significant difference between the number of Treg cells in health control people and ALL patients (P < 0.05). The results show that CD19 expression of the cases of B-ALL and CD7 expression of the cases of T-ALL had the highest positive rate; the levels of CD4+CD25+ Treg cells significantly increased in the peripheral blood of ALL patients.

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    Detection of Toll-like receptor 9 in peripheral blood mononuclear cells and serum tumor necrosis factor and Fas in patients with acute myeloid leukemia
    Qiu Yuan-xiu, Mo Dong-hua, Wang Xiao-tao
    2011, 15 (45):  8491-8494.  doi: 10.3969/j.issn.1673-8225.2011.45.029
    Abstract ( 297 )   PDF (529KB) ( 279 )   Save

    BACKGROUND: Toll-like receptor 9 (TLR9), tumor necrosis factor alpha (TNF-α) and Fas may together participate in the occurrence and development of acute myeloid leukemia (AML).
    OBJECTIVE: To study the expression of TLR9 in peripheral blood mononuclear cells (PBMNCs), levels of TNF-α and apoptosis-related genes in serum of patients with acute myeloid leukemia (AML).
    METHODS: The expression of TLR9 mRNA in PBMNCs of AML patients and normal control group was detected by reverse transcription-polymerase chain reaction (RT-PCR), the serum levels of TNF-α and Fas were detected were by enzyme-linked immunosorbent assay in each group.
    RESULTS AND CONCLUSION: Compared to normal control group, the expression of TLR9 mRNA in PBMNCs of in AML patients with untreated and refractory/relapsed groups was significantly increased (P < 0.01), and complete remission group was not statistically significant (P > 0.05). The serum levels of TNF-α and Fas in AML patients were significantly higher than those in the normal control group (P > 0.01). The expression of TLR9 was positively correlated with the serum levels of TNF- α and Fas.

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    Expression of mutant human hypoxia-inducible factor 1 alpha eukaryotic expression vector in bone marrow mesenchymal stem cells
    Zhang Nan, Li Chen, Guo Tao, Liu Dan-ping
    2011, 15 (45):  8495-8498.  doi: 10.3969/j.issn.1673-8225.2011.45.030
    Abstract ( 334 )   PDF (1419KB) ( 254 )   Save

    BACKGROUND: In vivo experiments of transgenic mice have shown that recombinant hypoxia-inducible factor 1 alpha (HIF-1α) can promote angiogenesis under the conditions of normal skin morphology and function.
    OBJECTIVE: To construct a new adenovirus eukaryotic expression vector that can co-express HIF-1α mutant protein and human renilla reniformis green fluorescent protein (hrGFP) reporter molecule under normoxia conditions to transfect bone marrow mesenchymal stem cells (BMSCs) of the Sprague-Dawley rats. 
    METHODS: A successful recombinant adenovirus eukaryotic expression vector pAd-HIF1αmu-IRES-hrGFP-1 was constructed and transfected into human embryonic kidney 293A cells (HEK293A) using Lipofectamine 2 000 for packaging the virus. The recombinant adenovirus eukaryotic expression vector was transfected into BMSCs of the rats at the best value multiplicity of infection 50. Three control groups were established: positive control group transfected with Ad-CMV-HIF1α-IRES-hrGFP-1, negative control group transfected with Ad-CMV-IRES-hrGFP-1 and blank control group without transfection.
    RESULTS AND CONCLUSION: ①The adenovirus vectors were transfected into the HEK293A cells with packaging successfully and a large amount of green fluoresence expression was found in the cells. ②The protein expression in the cells transfected with mutant adenovirus HIF-1α expression vector under normoxia conditions was higher than that of the three control groups. The difference among the three control groups had no significance(P > 0.05). To transfect mutant adenovirus eukaryotic expression vector pAd-HIF1αmu-IRES-hrGFP-1 into the HEK293A cells with pakaging successfully can induce the great and efficient expression of HIF-1α gene under normoxia conditions.

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    Time- and dose-dependent immunomodulatory effect of allogeneic mesenchymal stem cells in vivo
    Zhu Xi-shan, Shi Wei, Tai Wei-ping, Zhang Ge, An Guang-yu
    2011, 15 (45):  8499-8502.  doi: 10.3969/j.issn.1673-8225.2011.45.031
    Abstract ( 288 )   PDF (1603KB) ( 280 )   Save

    BACKGROUND: Allogeneic mesenchymal stem cells transplantation is widely used in clinics, but the required dose, duration and whether the side effects exists are still a research hotspot.
    OBJECTIVE: To study the time- and dose-dependent immunomodulatory effect of allogeneic bone marrow mesenchymal stem cells in vivo. 
    METHODS: Bone marrow-derived mesenchymal stem cells were isolated from mice with normal immune system. Twenty-four BALB/c mice were randomly divided into four groups. In experimental group, each mouse was injected with 0.3 mL cells suspension containing 5×105, 5×104, 5×103 bone marrow-derived mesenchymal stem cells via the tail vein, respectively. In control group, the mice were only injected with 0.3 mL normal saline. The lymphocyte proliferation test, mixed lymphocyte reaction and experiments about the effect of bone marrow-derived mesenchymal stem cells transplantation on the immune system of allogeneic mice were performed and detected.
    RESULTS AND CONCLUSION: After cell transplantation, bone marrow-derived mesenchymal stem cells exerted the in vivo immunomodulatory effect in a dose-dependent manner. Mesenchymal stem cells could promote the allogeneic graft implantation, and the immunomodulatory effect reached the peak at the 2nd week, gradually decreased at the 1st month and disappeared at the 2nd month. It is indicated that the immunomodulatory effects of mesenchymal stem cells are presented in a dose-dependent manner, which can only be maintained for some time.

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    Human umbilical cord mesenchymal stem cells induce ossification and treat bone defects
    Qu Zhi-guo, Ye Xiang-yang, Lin Hui, Cui Zheng-hong
    2011, 15 (45):  8503-8507.  doi: 10.3969/j.issn.1673-8225.2011.45.032
    Abstract ( 310 )   PDF (1774KB) ( 362 )   Save

    BACKGROUND: Umbilical cord mesenchymal stem cells have greater expansion capacity and low immunogenicity in ossification and tissue and organ repair, and their growth potential into a colony is earlier than mesenchymal stem cells of the bone marrow and other sources.OBJECTIVE: To observe the clinical effect of umbilical cords mesenchymal stem cells on inducing ossification and treating bone defects.
    METHODS: Human umbilical cord mesenchymal stem cells were isolated by the tissue block culture. In vitro osteogenic ability was confirmed by the morphology changes of human umbilical cord mesenchymal stem cells, alizarin red staining, alkaline phosphatase staining, and type Ⅰ collagen expression. Human umbilical cord mesenchymal stem cells transplantation was performed in patients with bone defects, and conditions of callus growth were regularly reviewed after transplantation.
    RESULTS AND CONCLUSION: In vitro induction experiments confirmed that umbilical cord mesenchymal stem cells had a clear osteogenic role. Two months after cell transplantation, X-rays showed bony callus formation, fracture interspace vague. Osseous connection formation was found at 3 months after cell transplantation. It was confirmed that umbilical cord mesenchymal stem cells exerted a role of osteogenic induction, and could repair bone defects via in vivo cell transplantation.

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    Stem cell mobilization and collection for autologous peripheral blood stem cells transplantation in diabetic foot treatment
    Li Hua, Chen Xu-yan, Zhou Bin, Feng Liang-hua, Xiao Ping-ping, Wu Wan-ting
    2011, 15 (45):  8508-8512.  doi: 10.3969/j.issn.1673-8225.2011.45.033
    Abstract ( 275 )   PDF (1521KB) ( 391 )   Save

    BACKGROUND: Autologous stem cell transplantation in the treatment of lower limb ischemia has been developed extensively in domestic and overseas and achieved better clinical curative effect. 5-10 μg/(kg • d) of granulocyte colony-stimulating factor (G-CSF) mobilization is often used, and stem cells are harvested after 5 days for transplantation. Whether the above-mentioned is the optimal mobilization scheme and harvesting opportunity is not reported.
    OBJECTIVE: To explore the best mobilizing scheme and harvesting opportunity and to increase the security of the treatment.
    METHODS: Eighteen diabetes foot patients preparing for stem cell transplantation were enrolled. G-CSF of 5-10 μg/(kg • d) was used for mobilizing hematopoietic stem cells. The relations between mobilization dose and days of G-CSF and the numbers of WBC, peripheral single nuclear cells and CD34+ were analyzed. Coagulation indexes and platelet count were detected before and after mobilization and collecting. Patients’ adverse effects were observed during process of acquisition and mobilization.
    RESULTS AND CONCLUSION: The acquisition efficiency of stem cells was closely related to mobilization dose and days of G-CSF. There were no significant changes in coagulation indexes before and after mobilization and collecting. Platelet count had no change before and after mobilization, but dropped dramaticlly after collecting .There was only one patient with mild bone ache and one patient who had a fever during the mobilization. Other patients all had no obvious adverse effects. The optimal time of stem cell collecting for patient with diabetic foot is decided by the number of peripheral blood mononuclear cells and CD34+ cells, not only by mobilization days and white blood cells counts. Mobilization and collecting of stem cells has a smaller effect on patients and a higher security.

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    Allogeneic hematopoietic stem cell transplantation versus immunosuppressive therapy as frontline treatment for severe aplastic anaemia
    Xu Yong, Ouyang Jian, Chen Bing, Yang Yong-gong, Xu Jing-yan, Zhou Rong-fu, Zhang Qi-guo, Shao Xiao-yan, Guan Chao-yang
    2011, 15 (45):  8513-8517.  doi: 10.3969/j.issn.1673-8225.2011.45.034
    Abstract ( 321 )   PDF (594KB) ( 377 )   Save

    BACKGROUND: Foreign reports have suggested that allogeneic hematopoietic stem cell transplantation (HSCT) and immunosuppressive therapy (IST) for acute severe aplastic anemia (SAA) have similar clinical effectiveness and overall survival period, but there are few reports about post-treatment quality of life and treatment costs of two different therapies.
    OBJECTIVE: To summarize the outcome and survival of both HLA matched sibling donor HSCT (allo-HSCT) and IST in 23 SAA patients.
    METHODS: Totally 7 patients with SAA who received allo-HSCT and 16 patients with SAA who received IST were selected from Department of Hematology, Nanjing Drum Tower Hospital from July 2004 to October 2010. Follow-up was performed every 3 months after treatment to observe the patients' survival, quality of life, cost of hospitalization and analyze the effects.
    RESULTS AND CONCLUSION: The allo-HSCT therapy was better than the IST therapy in the neutrophil and platelets recovery speed, the time of transfusion, the overall response rate after 3 months and the complete response rate after 1 year (P < 0. 05). The overall survival rates of the two therapies were 86% and 81.3% respectively, which had no significant difference (P > 0.05). The quality of life was good at 1 year after treatment. There was no statistically significant difference between the two therapies in total efficacy rates, physiological state, psychological state, social relationships, and environmental condictions one year later. The costs of hospitalization between the two groups were similar.

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    Adult stem cells and lung regeneration
    Su Shen, Sun Hai-yan, Zhang Tong, Wu Li-jun, Yao Ji-rong
    2011, 15 (45):  8520-8524.  doi: 10.3969/j.issn.1673-8225.2011.45.036
    Abstract ( 280 )   PDF (623KB) ( 289 )   Save

    BACKGROUND: Stem cells with active homing function and regulation has a great application prospect to lung regeneration due to the lung tissue with complex structure and long disease cycle.
    OBJECTIVE: To overally understand the progress of adult stem cells in treatment of lung diseases and injury.
    METHODS: The first author retrieved PuMed for articles about adult stem cells for lung injury published before 2011. Repetitive articles were excluded.
    RESULTS AND CONCLUSION: Totally 135 articles were retrieved, and finally 50 articles were included in result analysis. Bone marrow-derived mesenchymal stem cells as the representative of adult stem cells have a strong multi-differentiation potential for the treatment of lung disease, which can involved in wound healing and tissue regeneration. However, the therapeutical mechanism and related influential factors need further studies.

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    Colon cancer stem cell surface markers and signal transduction research
    Chen Yuan-chong
    2011, 15 (45):  8525-8528.  doi: 10.3969/j.issn.1673-8225.2011.45.037
    Abstract ( 267 )   PDF (532KB) ( 450 )   Save

    BACKGROUND: In recent years, studies have shown that colon cancer stem cells are involved in tumor recurrence and metastasis, which have brought a new hope for cancer targeted therapy.
    OBJECTIVE: To investigate the isolation and identification method of colon cancer stem cell surface markers as well as relevant signal transduction pathways.
    METHODS: A computer-based search of Medline and CNKI databases (2000-01/2011-06) was performed to retrieve colon cancer stem cell surface markers and signal transduction using the keywords of “colon cancer stem cell, cancer stem cell, cell surface sign, signal transduction” in English and Chinese, respectively. Repetitive articles or Meta analyses were excluded, and finally 40 articles were included in result analysis.
    RESULTS AND CONCLUSION: CD133+ and CD44+ are used as colon cancer stem cell surface markers. Closely related to colon cancer stem cells, Wnt signaling pathway plays an important role in stem cell homeostasis, and Notch signaling pathway is a major stem cell signaling pathway. Based on studies of colon cancer stem cell surface markers, the early presence of the tumor can be detected; to grasp the biological characteristics of colon cancer stem cells and signal transduction pathway can reduce tumor recurrence, and reduce the difficulty in diagnosis and treatment of colon cancer.

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    Endothelial progenitor cells and estrogen
    Liu Teng, Zhao Qian, Wang Wen
    2011, 15 (45):  8529-8532.  doi: 10.3969/j.issn.1673-8225.2011.45.038
    Abstract ( 297 )   PDF (608KB) ( 291 )   Save

    BACKGROUND: Estrogen has obviously protective effect on vascular endothelium. Endothelial progenitor cells (EPCs), as precursors of endothelial cells, take an important role in endothelial recovery.
    OBJECTIVE: To summarize the characteristics of EPCs as well as the effect of estrogen on EPCs.
    METHODS: A computer search of PubMed database and CNKI database was performed using the keywords of “endothelial progenitor cells, estrogen” in English and Chinese, respectively, in the titles and abstracts. All articles related to the characteristics of endothelial progenitor cells and studies about the effect of estrogen on EPCs were selected.
    RESULTS AND CONCLUSION: EPCs are the precursors of endothelial cells which have the capacity of proliferation, migration, adhesion and differentiation into vascular endothelial cells. EPCs are existing in both bone marrow and peripheral blood, which has become a new therapy target of cardiovascular diseases. Studies have shown that estrogen has protective effect on EPCs: estrogen can improve the proliferation, migration, adhesion and other bioactivities of EPCs, and EPCs senescence are delayed and apoptosis of EPCs are reduced by estrogen treatment. Further research is needed to clarify the specific targets and mechanisms involved in the effect of estrogen on EPCs.

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    Research progress in biological pacemakers
    Tian Ye, Zhang Chen-yun
    2011, 15 (45):  8533-8536.  doi: 10.3969/j.issn.1673-8225.2011.45.039
    Abstract ( 320 )   PDF (583KB) ( 304 )   Save

    BACKGROUND: Biological pacemakers need not replace battery, can approach magnetic field, and has automatic reaction to the neurotransmitter inside the body. It is an effective method to treat cardiac conduction system disease.
    OBJECTIVE: From gene treatment, cell transplantation, hormone curing to acquaint the methods of building biological pacemakers.
    METHODS: Using “biological pacemaker” as a keyword in Chinese and English, a computer-based search of Wanfang and PubMed databases (2000-03/2009-03) was conducted to retrieve relevant articles. Among the 105 retrieved articles, 25 articles were included in result analysis.
    RESULTS AND CONCLUSION: Currently, there are three kinds of methods to build biological pacemakers: gene transfection, cell transplantation and hormone cure. The research of biological pacemaker is still placed in the animal experimental step, and it has a long way to go until the biological pacemakers can be used clinically, such as how to acquire safe and efficient gene vectors, the best part for cell transplantation, how to adjust the pacing function and how to handle the immunity reject reaction, etc. We believe according to the developing of cell biology, cell electricity physiology, molecular biology and genetic engineering technology, the problems that exist currently will gradually be settled and biologic pacemakers will become an effective way to treat cardiac conduction system disease.

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    Analysis of policy, funds and research and development on stem cell in U.S.A.
    Fu Jun-ying, Zhao Yun-hua
    2011, 15 (45):  8537-8541.  doi: 10.3969/j.issn.1673-8225.2011.45.040
    Abstract ( 413 )   PDF (696KB) ( 423 )   Save

    BACKGROUND: U.S.A scientists have conducted the top-level researches on stem cells all over the world; however, the related governance and policies are changed all the time.
    OBJECTIVE: To study changes on policies and investments conducted by U.S.A. governments and companies, and potential great influences on global patterns.  
    METHODS: SCI database (http://isiknowledge.com), Wanfang database (http://www.wanfangdata.com.cn), VIP database (http://www.vmis.net.cn/yixue/index.asp), official website of NIH (http://www.nih.gov/), and reports released by GBI Research, were searched by the first author. Search terms were “stem cell, USA, policy, invest” in English and “stem cell, USA” in Chinese. 128 papers related to policies and investments on stem cell in U.S.A. were retrieved, and there were 30 papers matching research requirements after excluding old, repeated and similar materials.  
    RESULTS AND CONCLUSION: Debates on policies and investments on stem cell in U.S.A. mostly focus on if federal funds could be used for research on human embryonic stem cell (hESC), and there is not much limitation on non-federal funds supporting on hESC research. The limitation on hESC research supported by federal funds has partly loosed than before after accession of President Obama, though it has not resulted in consequent and immediate effects yet. There is a promising perspective on research and industry in field of stem cell because of strong supports from local governments and individuals, as well as enormous investment from industries, though funds issued by federal government have been limited in U.S.A. And hESC may become the priority field in the future.

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    In vitro experiment of umbilical cord mesenchymal stem cells to promote bone healing and clinical application in one case
    Li Hua-tao, Bian Lin-fen, Wu Sheng-gang, Li Qiang, Wang Li-li, Dai Yu-cheng, Liu Yang
    2011, 15 (45):  8542-8546.  doi: 10.3969/j.issn.1673-8225.2011.45.041
    Abstract ( 236 )   PDF (700KB) ( 382 )   Save

    BACKGROUND: Umbilical cord mesenchymal stem cells (UCMSCs) are more original than adult ones. Studies have shown that UCMSCs have higher telomerase activity, shorter culture doubling time and wider lineage differentiation.
    OBJECTIVE: To explore the potency of UCMSCs differentiated into osteoblasts in vitro and their clinical effects on bone nonunion.
    METHODS: UCMSCs were isolated from Wharton’s jelly of human umbiIical cord; after serial subculture in vitro, MSCs were tested for their immunophenotype and osteogenic differentiation. Clinical application of UCMSCs transplantation was also performed to a patient with refractory exposed bone fracture evoked by infection.
    RESULTS AND CONCLUSION: UCMSCs exhibited fibroblastic morphology and long-term stable culture. These passaged cells presented MSCs immunophenotype and there were a great amount of calcium deposition and nodes in intracytoplasm detected by alizarin red and Von Kossa staining, respectively, after osteogenic differentiation. The patient was treated with UCMSCs suspension for four times, granulation tissue grew rapidly to fulfill the sinus tract and became epithelized. Twelve days after treatment, the fracture was healed. It indicates that UCMSCs have self-renewal and pluripotent differentiation potential and can differentiate into osteoblasts in vitro. For treatment of bone nonunion, UCMSCs has the ability to improve microenvironment.

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    Granulocyte-colony stimulating factor related lung injury in a leukemia patient during mobilization of peripheral blood stem cells
    Shi Bing, Liu Li-hui, Ye Li-ping
    2011, 15 (45):  8547-8550.  doi: 10.3969/j.issn.1673-8225.2011.45.042
    Abstract ( 295 )   PDF (558KB) ( 307 )   Save

    BACKGROUND: There are few studies about granulocyte-colony stimulating factor related lung injury during mobilization of peripheral blood stem cells, but the mechanism is unclear.
    OBJECTIVE: To explore the clinical manifestation and possible pathogenic mechanism of acute lung injury related to recombinant human granulocyte-colony stimulating factor.
    METHODS: We reported a case of sudden hemoptysis, scattered lung nodular shadows and patchy shadows in a leukemia patient following the administration of granulocyte-colony stimulating factor to mobilize peripheral blood stem cells, and related literatures were also reviewed.
    RESULTS AND CONCLUSION: Granulocyte-colony stimulating factor while mobilizing peripheral blood stem cells could induce acute lung injury, which may involve migration of neutrophils to vascular spaces, adhesion of neutrophils to endothelial cells, and potentiation of proinflammatory cytokine expression.

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