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    05 February 2015, Volume 19 Issue 6 Previous Issue    Next Issue
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    Human telomerase reverse transcriptase-mediated effects on biological characteristics of rat fetal liver stem cells
    Ren Li-gang, Dai Xiang-chen
    2015, 19 (6):  821-825.  doi: 10.3969/j.issn.2095-4344.2015.06.001
    Abstract ( 338 )   PDF (709KB) ( 512 )   Save

    BACKGROUND: Studies have shown that stem cells transfected with human telomerase reverse transcriptase (hTERT) gene can stably express high-level telomerase activity and strengthen cell proliferation, which lays the foundation to establish genetically engineered immortalized stem cell lines.
    OBJECTIVE: To explore the effects of hTERT transfection on proliferation and cell cycle of rat fetal liver stem cells in vitro.
    METHODS: Rat fetal liver stem cells cultured in vitro were transfected by recombinant adeno-associated virus carrying hTERT genes. RT-PCR and western blot assay were used to detect the expression of hTERT mRNA and protein, respectively. Cell Counting Kit-8 method and cell growth curve were used to detect cell growth and proliferation. Changes in cell cycle distribution were determined by flow cytometry.
    RESULTS AND CONCLUSION: Compared with the control group and empty virus group, in the hTERT infection group, hTERT expressed at gene and protein levels, the growth rate of the cells increased, and the number of cells at G0/G1 phase and S phase was decreased and increased, respectively. The results show that recombinant adeno-associated virus as a vector of hTERT gene used for gene transfection can promote the in vitro proliferation of rat fetal liver stem cells and play an optimal role in cell culture.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Role of hypoxia-inducible factor 1 alpha and inducible nitric oxide synthase in neural stem cells during hypoxia/reoxygenation injury
    Li Ying
    2015, 19 (6):  826-831.  doi: 10.3969/j.issn.2095-4344.2015.06.002
    Abstract ( 456 )   PDF (770KB) ( 541 )   Save

    BACKGROUND: Organism in the hypoxic state can produce hypoxia-inducible factor, but nitric oxide generated from inducible nitric oxide synthase can inhibit the activity of hypoxia-inducible factor 1α.
    OBJECTIVE: To discuss the relationship of hypoxia-inducible factor 1α and inducible nitric oxide synthase with hypoxia/reoxygenation injury in neural stem cells.
    METHODS: Under sterile conditions, Wistar rats born within 24 hours were sacrificed to separate the rat hippocampus that was used to prepare a cell suspension of brain tissue. After culture and passage, neural stem cells were divided into normoxia, hypoxia and hypoxia/reoxygenation groups. In the latter two groups, 150 μmol/L cobalt chloride solution was used to prepare hypoxia models, and in the hypoxia/reoxygenation group, the cells were reoxygenated after 4-hour hypoxia.
    RESULTS AND CONCLUSION: Under hypoxic conditions, a significant increase in mRNA expressions of hypoxia-inducible factor 1α and inducible nitric oxide synthase as well as the number of apoptotic neural stem cells. Compared with the hypoxia group, the number of apoptotic neural stem cells was higher in the hypoxia/reoxygenation group, but the mRNA expressions of hypoxia-inducible factor 1α and inducible nitric oxide synthase were lower. These findings indicate that these two factors are involved in the hypoxia/reoxygenation injury of neural stem cells.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Bone marrow mesenchymal stem cells are induced directly to differentiate into chondrocytes in osteoarthritis patients
    Guo Hong-liang, Tie Xiao-jia, Han Ya-jun, Xu Chao, Wang Zhi-zhou, Wang Xin, Wang Jun-feng, Guan Zhen-peng, Bi Xiao-juan, Yilihamu Tuoheti
    2015, 19 (6):  832-836.  doi: 10.3969/j.issn.2095-4344.2015.06.003
    Abstract ( 337 )   PDF (1830KB) ( 483 )   Save

    BACKGROUND: In recent years, many reports have focused on inflammatory cytokines, growth factors and mechanical loads affecting the cartilage and subchondral regeneration, but there is a lack of comprehensive understanding about the mechanism of osteoarthritis.
    OBJECTIVE: To explore the correlation between function status of bone marrow mesenchymal stem cells and disease progression in patients with osteoarthritis.
    METHODS: Femoral bone marrow was extracted from patients with femoral neck fractures (control group), mild (mild group) and severe (severe group) osteoarthritis to isolate and culture bone marrow mesenchymal stem cells. Cell counting kit-8 was used to detect the proliferative ability of bone marrow mesenchymal stem cells from 
    different patient groups, and passage 3 bone marrow mesenchymal stem cells were subject to 2-week chondrogenic induction followed by toluidine blue staining.
    RESULTS AND CONCLUSION: Bone marrow mesenchymal stem cells were isolated and cultured from the femoral bone marrow of different groups. The proliferative ability of cells in the control group was significantly higher than that in the mild and severe groups. After chondrogenic induction, bone marrow mesenchymal stem cells varied obviously in the morphology that was from fusiform to qusi-circular or polygon, the percentage of nucleoplasm became smaller, and cells were positive for toluidine blue staining. The number of chondrocytes generated in the severe group was less than that in the control group, but there was no great difference in cell morphology. These findings indicate that the occurrence of osteoarthritis is negatively correlated with the functional status of autologous bone marrow mesenchymal stem cells.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Effect of bone morphogenetic protein 7 adenovirus transfection on biological function of bone marrow stromal stem cells
    Pu Zhi-chao, Xie Wei-yong, Wang Yan-bin, Xue Jian, Zhang Xing-shi
    2015, 19 (6):  837-842.  doi: 10.3969/j.issn.2095-4344.2015.06.004
    Abstract ( 312 )   PDF (2459KB) ( 546 )   Save

    BACKGROUND: Gene transfer techniques have been actively used in tissue regeneration therapy. Bone morphogenetic protein 7 with osteoinductive properties can effectively promote osteoblast growth and new bone formation.
    OBJECTIVE: To explore the influence of bone morphogenetic protein 7 adenovirus gene transfection on the biological function of bone marrow stromal stem cells.
    METHODS: Goat bone marrow stromal stem cells were isolated, cultured and transfected by recombinant adenovirus containing bone morphogenetic protein 7 (Adeno-BMP7). Cell ultrastructure was observed by transmission electronic microscope, cell cycle was detected by flow cytometry, expression of bone morphogenetic protein 7 was measure by western blot assay, and Von Kossa staining was used to observe the formation of calcium nodules. Bone marrow stromal stem cells transfected for 3 days and untransfected were used to prepare coral-cell complexes that were injected subcutaneously into the back of nude mice for 4 weeks and 8 weeks, followed by gross observation and histological examination.
    RESULTS AND CONCLUSION: Adeno-BMP7-transfected bone marrow stromal stem cells appeared to have active substance synthesis and metabolism. Adeno-BMP7 transfection played no effect on the cell cycle of bone marrow stromal stem cells. Bone morphogenetic protein 7 was expressed in the transfected bone marrow stromal stem cells. Larger calcium nodules were visible after Adeno-BMP7 transfection. Adeno-BMP7-transfected bone marrow stromal stem cells showed stronger osteogenic capability and higher bone quality. These results demonstrate that Adeno-BMP7 transfection can effectively promote the osteogenic differentiation of bone marrow stromal stem cells.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Effects of stromal cell-derived factor-1 on bone marrow mesenchymal stem cells migration and skin wound repair
    Ding Yue, Xu Hai-long, Song Cong-xiao, Sun Xiao-ju
    2015, 19 (6):  843-848.  doi: 10.3969/j.issn.2095-4344.2015.06.005
    Abstract ( 346 )   PDF (2463KB) ( 585 )   Save

    BACKGROUND: Stromal cell-derived factor-1 has a strong chemotaxis to bone marrow mesenchymal stem cells, and both of them can promote wound healing. However, there are less studies on their correlation with skin wound healing.
    OBJECTIVE: To investigate the effects of stromal cell-derived factor-1 on bone marrow mesenchymal stem cells migration and skin wound repair.
    METHODS: Thirty SD rats were divided into five groups at random. Bone marrow mesenchymal stem cells labeled with PKH-26 were injected into the rat caudal vein. After 1 week, skin wound models were established. Then, different concentrations (1, 2, 10, 50 μg/L) of stromal cell-derived factor-1 were injected via multi-points on the skin wound. The skin wound healing was observed and recorded at 14 days after injection. The number and distribution of bone marrow mesenchymal stem cells were observed by the fluorescent staining at different time points. The pathological changes of wound tissue were observed by hematoxylin-eosin staining. The expression of collagen I and collagen III were detected by western blot assay.
    RESULTS AND CONCLUSION: Stromal cell-derived factor-1 at 10 μg/L could induce the largest number of bone marrow mesenchymal stem cells to the skin wound and achieve the best repair results. Stromal cell-derived factor-1 could also regulate the expression of collagen I and collagen III in the wound, and when the concentration 
    of stromal cell-derived factor-1 was 10 μg/L, the expressions of collagen I and collagen II reached the peak. These findings indicate that the appropriate concentration of stromal cell-derived factor-1 is better to promote the migration of bone marrow mesenchymal stem cells, thereby contributing to skin wound repair.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Imatinib resistance of K562 cells co-cultured with bone marrow stromal cells from patients with chronic myeloid leukemia
    Wang Ji-gang, Zhang Hai-ting, Zhou Fan, Liu Yan-qin, Bai Ying, Liu Jing-hua, Li Min-yan
    2015, 19 (6):  849-853.  doi: 10.3969/j.issn.2095-4344.2015.06.006
    Abstract ( 377 )   PDF (1862KB) ( 464 )   Save

    BACKGROUND: Imatinib resistance is a key issue in treatment of chronic myeloid leukemia. It is confirmed that the leukemia cells can obtain drug resistance phenotype mediated by adhesion to the bone marrow stromal cells (BMSCs). But, the role of BMSCs in imatinib resistance is unclear because chronic myeloid leukemia is deficient in adhesion function.
    OBJECTIVE: To in vitro simulate the bone marrow microenvironment of patients with chronic myeloid leukemia and to explore its influences on imatinib sensitivity as well as possible mechanisms.
    METHODS: BMSCs isolated from patients with chronic myeloid leukemia but not undergoing treatment were co-cultured with K562 cells to construct the BMSCs-K562 cell co-culture model in chronic myeloid leukemia 
    patients, then exposed to 0.2-3.2 μmol/L imatinib for 48 hours, and the proliferation inhibition rate of K562 cells was studied by MTT assay. The apoptosis rate of K562 cells and the expression of the CXCR4 in K562 cells exposed to
    0.5 μmol/L imatinib for 72 hours were detected by flow cytometry. The K562 cells were exposed to 0.5 μmol/L imatinib for 4 hours and labeled by Calcein-AM fluorescent labeling sytem, and then, the adhesion rate of the K562 cells was calculated based on fluorescence intensity.
    RESULTS AND CONCLUSION: The suppressing effect of imatinib (0.2-3.2 μmol/L) on the proliferation of K562 cells was weakened significantly by co-culture with the bone marrow stromal cells from patients with chronic myeloid leukemia. The apoptosis rate of K562 cells exposed to 0.5 μmol/L imatinib for 72 hours in co-culture group was significantly lower than that in the suspension culture group (P=0.020). The positive rates of CXCR4 in the co-culture group and suspension culture groups were both increased after exposure to 0.5 μmol/L imatinib for 72 hours (P=0.001). The adhesion rate of the K562 cells to the BMSCs was elevated from (32.18±6.17)% to (68.97±11.08)% when the K562 cells were exposed to 0.5 μmol/L imatinib for 4 hours, and the difference had statistical significance (P=0.022). These findings indicate that the co-culture with the BMSCs from patients with chronic myeloid leukemia can mediate K562 cells resistance to imatinib, which may be related to that the co-culture with BMSCs and exposure to imatinib can induce the K562 cells to express CXCR4. But the mechanism needs in-depth studies.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Isolation and culture of mouse adipose-derived stem cells and their homing to the intestinal tract
    Hou Xiao-lin, Yu Wei-dong, Cui Mei-hua, He Xiang-jun, Liang Jun
    2015, 19 (6):  854-860.  doi: 10.3969/j.issn.2095-4344.2015.06.007
    Abstract ( 524 )   PDF (2407KB) ( 926 )   Save

    BACKGROUND: Adipose-derived mesenchymal stem cells have gained more and more attention due to their high safety, less invasiveness, easy purification and rapid proliferation.
    OBJECTIVE: To isolate and culture adipose-derived mesenchymal stem cells efficiently and rapidly with high purity and then to explore the cell homing to the intestinal tract after fluorescence labeling.
    METHODS: Mouse adipose tissue obtained from the groin and epididymis was aseptically isolated and digested with 0.1% collagenase I. Then the digested cells and undigested adipose tissue were cultured together in the dish to harvest adipose-derived mesenchymal stem cells. The cells were identified by morphology, surface markers, growth kinetics, osteogenic and adipogenic differentiation potential, and then labeled by PKH67 before injected into ulcerative colitis mouse models through the tail vein to observe their homing to the intestinal tract. 
    RESULTS AND CONCLUSION: In vitro, adipose-derived mesenchymal stem cells isolated by this method exhibited spindle-like appearance, grew intensively and arranged in a swirling shape. Adipose-derived mesenchymal stem cells expressed CD29, CD44 and CD90, but not expressed CD45. After osteogenic induction, alkaline phosphatase staining showed black particles and alizarin red S staining showed red mineralized nodules. After adipogenic induction, oil red O staining showed many lipid droplets were dyed red. Cell growth curve showed cells at 3-5 days were in logarithmic growth phase and they were active. Under fluorescence microscopy, frozen sections of the colon were found green fluorescence points that were increased with time. Results suggest that adipose-derived mesenchymal stem cells isolated and cultured in vitro can proliferate rapidly, purify easily and can be induced to osteoblasts and adipocytes; in vivo, PKH67-labeled cells can home to and proliferate in the colon.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Role of P2X7 receptor in osteogenic differentiation of periodontal ligament stem cells
    Sun Ya-nan, Wei Jian-min, Sun Wei, Wu Jun-jie, Wu Li-an
    2015, 19 (6):  861-867.  doi: 10.3969/j.issn.2095-4344.2015.06.008
    Abstract ( 348 )   PDF (5867KB) ( 803 )   Save

    BACKGROUND: Ion channels related to the osteogenic differentiation of periodontal ligament stem cells have been studied.
    OBJECTIVE: To preliminarily investigate the effect of P2X7 receptor on the osteogenic differentiation of human periodontal ligament stem cells.
    METHODS: Human periodontal ligament stem cells were isolated and divided into four groups, cultured in
    100 nmol/L adenosine triphosphate+osteogenic medium, osteogenic medium, 100 nmol/L adenosine triphosphate, and normal culture medium (control group), respectively. After induction for 7 and 14 days, osteogenic effect was detected by alizarin red staining, and expressions of OCN, Runx2 and P2X7 receptor at mRNA and protein levels were analyzed by qRT-PCR and western blot assay, respectively.
    RESULTS AND CONCLUSION: Under alizarin red staining, the osteogenic effect of periodontal ligament stem 
    cells was better in the group of adenosine triphosphate+osteogenic medium than the osteogenic medium group at 7 days, but it was better in the osteogenic medium group than the group of adenosine triphosphate+osteogenic medium at 14 days (P < 0.05). Results from qRT-PCR showed that, in the group of adenosine triphosphate+osteogenic medium, the mRNA expression of Runx2 and OCN reached peak at 7 days, but decreased significantly at 14 days (P < 0.05). The expression of P2X7 receptor mRNA in the group of adenosine triphosphate+osteogenic medium was significantly higher than that in the adenosine triphosphate group at 7 days (P < 0.05), but significantly lower than that in the adenosine triphosphate group at 14 days (P < 0.05). There was no expression of P2X7 receptor mRNA in the osteogenic medium group and control group. Western blot assay showed that at 7 days, the expression of P2X7 receptor peaked in the adenosine triphosphate+osteogenic medium group at 7 days, which was significantly higher than that in the adenosine triphosphate group, and there was a low expression of P2X7 receptor in the osteogenic medium group and no expression in the control group; at 14 days, the expression of P2X7 receptor decreased significantly in the adenosine triphosphate+osteogenic medium group but increased in the adenosine triphosphate group. Experimental findings show that exogenous adenosine triphosphate could significantly improve the osteogenic differentiation of periodontal ligament stem cells at 7 days, but after that, inhibit the osteogenic differentiation; exogenous adenosine triphosphate could activate the expression of P2X7 receptor in periodontal ligament stem cells, and P2X7 receptor expression has positive correlation with the osteogenic differentiation of periodontal ligament stem cells.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Establishment of human induced pluripotent stem cell lines
    Shi Ying-xu, Han Yan-qiu, Xie Yin-liang, Du Hua
    2015, 19 (6):  868-875.  doi: 10.3969/j.issn.2095-4344.2015.06.009
    Abstract ( 427 )   PDF (2443KB) ( 544 )   Save

    BACKGROUND: Induced pluripotent stem cells have a generating process similar to cancer stem cells and possess stem cell characteristics extremely close to human embryonic stem cells. Therefore, studies on induced pluripotent stem cells are in favor of an increased awareness and understanding of human development and tumor occurrence.
    OBJECTIVE: To master the technology of establishing induced pluripotent stem cell lines in order to build the technology platform for reprogramming specific disease cells, thus to explore the pathogenesis of the disease using reprogramming technology.
    METHODS: Retroviruses containing Oct4, Sox2, Klf-4, and c-Myc4 transcription factors were used to transfect human skin fibroblasts (HS27 cells), and then the cells were induced to differentiate to human embryonic stem cell-like clones in the human embryonic stem cell culture conditions. The cells were picked and further amplified. After observation of clone morphology and alkaline phosphatase activity test, immunofluorescence detection was used to detect whether human embryonic stem cell markers Oct4, Sox2, c-Myc, Klf-4 expressed, the pendant-drop method was used to detect the ability of HS27-derived clones to form teratomas and verify the  differentiation into three germ layers.
    RESULTS AND CONCLUSION: After viral infection, embryonic stem cell-like clones formed and were negative for green fluorescent proteins. These clones were similar to human embryonic stem cell clones in cell morphology. After further amplification, they were positive for alkaline phosphatase. Immunofluorescence results showed that the clones expressed Oct4, Sox2, c-Myc, Klf-4, and HS27 cells-derived clones injected into immunodeficient mice could form teratomas and had the ability to differentiate into the three germ layers under hematoxylin-eosin staining. In this experiment, induced pluripotent stem cell lines were successfully constructed, laying a good experimental foundation for disease-specific cell reprogramming research.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Effect of oxygen-glucose deprivation on the proliferation, differentiation and apoptosis of neural stem cells
    Ma Jun-ning,Gao Jun-wei, Hou Bo-ru, Ren Hai-jun, Chen Si-hua, Liu Ji-xing, Yan Gui-zhong
    2015, 19 (6):  876-882.  doi: 10.3969/j.issn.2095-4344.2015.06.010
    Abstract ( 427 )   PDF (2548KB) ( 434 )   Save

    BACKGROUND: Hypoxia is one of the main pathological factors of nervous system diseases, which plays numerous regulatory roles in survival, migration, differentiation, apoptosis of endogenous neural stem cells and exogenous neural stem cells after transplantation.
    OBJECTIVE: To systematically observe the effects of oxygen-glucose deprivation on the proliferation, differentiation and apoptosis of neural stem cells.
    METHODS: Neural stem cells were isolated from the olfactory bulb of newborn Kunming mice, to establish oxygen-glucose deprivation models. Immunofluorescence technique was used to determine the differentiation ability of neural stem cells subject to oxygen-glucose deprivation, MTT method was used to measure the proliferative ability of neural stem cells under normoxic conditions after oxygen-glucose deprivation for 24 hours and 48 hours, and Hochest 33258 staining was performed to detect the apoptosis of neural stem cells after oxygen-glucose deprivation for 24 hours and 48 hours.
    RESULTS AND CONCLUSION: Passage 4 neural stem cells were positive for CD133. Compared with the normoxic group, MTT showed that the proliferation of neural stem cells was significantly lower in the oxygen-glucose deprivation group (P < 0.05), moreover, the proliferative ability of neural stem cells was lower in 
    the 48-hour oxygen-glucose deprivation group than the 24-hour oxygen-glucose deprivation group (P < 0.05). The number of GFAP and β-Tubulin III positive cells was significantly lower in the 48-hour oxygen-glucose deprivation group than the normoxic group (P < 0.05). Apoptotic rate was significantly increased after oxygen glucose deprivation for 48 hours as compared with oxygen-glucose deprivation for 24 hours (P < 0.01) and normoxic group (P < 0.01). These results indicate that oxygen-glucose deprivation have adverse effects on neural stem cell proliferation, differentiation and apoptosis, and its impact depends on the concentration and time of hypoxia as well as the ability of tolerance to hypoxia.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Bone marrow mesenchymal stem cell transplantation combined with core decompression and bone grafting in the repair of osteonecrosis of femoral head
    Zhang Yang, Wang Nan, Yang Li-feng, Ma Ji, Li Zhi
    2015, 19 (6):  883-890.  doi: 10.3969/j.issn.2095-4344.2015.06.011
    Abstract ( 351 )   PDF (442KB) ( 484 )   Save

    BACKGROUND: Core decompression alone for osteonecrosis of femoral head easily causes fovea of femoral head and collapse of inner microstructure. Therefore, autologous bone is needed for filling and supporting. Moreover, bone marrow stem cell transplantation can decrease the incidence of femoral head collapse.
    OBJECTIVE: To discuss the clinical effects of core decompression and bone grafting combined with autotransplantation of bone marrow mesenchymal stem cells for osteonecrosis of femoral head.
    METHODS: A total of 33 patients were treated by core decompression and bone grafting combined with autotransplantation of bone marrow mesenchymal stem cells in the Fourth Department of Bone Surgery, Central Hospital Affiliated to Shenyang Medical College in China from December 2012 to May 2013.
    RESULTS AND CONCLUSION: After the treatment by core decompression and bone grafting combined with autotransplantation of bone marrow mesenchymal stem cells, Harris hip function score increased and pain disappeared in patients with osteonecrosis of femoral head. They could do various labors. Radiographs or CT examination displayed normal femoral head in 30 hips, accounting for 79%. Pain significantly reduced. Normal or slight limp walking was found in 15 hips, accounting for 40%. There were 35 hips in patients, whose walking distance was extended, accounting for 92%. 24 hips dysfunction was improved markedly, accounting for 63%. All results suggested that core decompression and bone grafting combined with autotransplantation of bone marrow mesenchymal stem cells improved the local blood supply of femoral head, and played a positive role in promoting the necrotic bone absorption and bone repairing.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Autogenous bone marrow mesenchymal stem cells carrier complex for bone defect repair: a histological observation 
    Han Cao1, Ma Ning2, Li Zhong-yi1, Wang Zheng-dong3, Yan Nan3, Zhu Shi-long4
    2015, 19 (6):  891-897.  doi: 10.3969/j.issn.2095-4344.2015.06.012
    Abstract ( 381 )   PDF (1052KB) ( 663 )   Save

    BACKGROUND: Autogenous bone is the best choice for the repair of bone defects from the aspects of repair quality, immune rejection and disease transmission, but the limited sources and complications after bone collection bring a big limitation for bone defect repair and clinical application of autogenous bone graft.
    OBJECTIVE: To repair the bone defects with demineralized bone carrying autologous bone marrow mesenchymal stem cells and meanwhile to inject basic fibroblast growth factor and other factors into the micro-environment at the implant site, in order to enhance bone repair capacity and improve the repair effect.
    METHODS: Forty-five New Zealand white rabbits at an age of 3 months were selected to establish bone defect models (the lower segment of bilateral forearm bone-periosteum), and then, the animals were divided into three groups: experimental, control and blank groups. Bone marrow samples were extracted from the left iliac bone and femoral trochanter. Bone marrow mesenchymal stem cells were isolated, cultured and amplified followed by co-cultured with different materials in vitro, and then, the composite scaffolds were implanted to the bone defects of the radial shaft. In the experimental group, bone marrow mesenchymal stem cells, demineralized bone, calcium alginate, basic fibroblast growth factor, vitamin C were implanted; in the control group, bone marrow 
    mesenchymal stem cells, demineralized bone, calcium alginate were implanted; in the blank group, nothing was implanted.
    RESULTS AND CONCLUSION: At 30, 60, 90 days after implantation, there were significant differences in the new bone formation rate and new bone amount between different groups. The bone formation speed and material degradation speed were significantly faster in the experimental group than the control and blank groups, while the amount of remnants at the defect region was larger in the latter two groups. Multi-point bone formation was visible in the experimental group, while “creeping substitution” was found in the control and blank group. At 90 days after implantation, bone defects were not healed in the blank group undergoing natural healing. These findings indicate that co-transplantation of bone graft and basic fibroblast growth factor and vitamin C is beneficial to bone repair and improves bone defect healing.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Mouse embryonic stem cell transplantation for treatment of osteoporosis
    Fan Zhi-gang, Wang Dong
    2015, 19 (6):  898-902.  doi: 10.3969/j.issn.2095-4344.2015.06.013
    Abstract ( 324 )   PDF (710KB) ( 442 )   Save

    BACKGROUND: Because of poor therapeutic effects of drug treatment, stem cell transplantation has become a hot spot in the treatment of osteoporosis.
    OBJECTIVE: To investigate the therapeutic efficacy of embryonic stem cell transplantation in the treatment of estrogen deficiency-induced osteoporosis.
    METHODS: Thirty female healthy C57BL/6 mice were randomly divided into model, sham-operated, and treatment groups, with 10 mice in each group. Ovariectomized models were established. In the treatment group, embryonic stem cells were injected by tail vein at 1 day after modeling, and there was no treatment in the other two groups. After 10 hours of treatment, flow cytometry was used to detect the apoptosis of T-lymphocytes; after 3 days of treatment, ELISA assay was used to detect the level of tumor necrosis factor-α in mouse serum; after
    1 month of treatment, micro-CT was employed to determine the number of bone trabeculae and bone mineral density.
    RESULTS AND CONCLUSION: Compared with the sham-operated group, the number of bone trabeculae and bone mineral density were lower in the model group, while the serum level of tumor necrosis factor-α was higher in the model group. After embryonic stem cell transplantation via the tail vein, the number of bone trabeculae and the bone volume fraction were increased certainly, the serum level of umor necrosis factor-α was decreased, and the number of apoptotic T-lymphocytes was increased in the treatment group, which significantly differed from those in the model group (P < 0.05). These findings indicate that embryonic stem cell therapy has a certain effect on the treatment of osteoporosis, which may play a role through immune regulation.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Human telomerase reverse transcriptase transfection of bone marrow mesenchymal stem cells in the treatment of diabetic rats
    Zhao Hai-lian
    2015, 19 (6):  903-907.  doi: 10.3969/j.issn.2095-4344.2015.06.014
    Abstract ( 321 )   PDF (734KB) ( 479 )   Save

    BACKGROUND: Human telomerase reverse transcriptase (hTERT) is the first choice for regulating the proliferation and directional differentiation, with multiple biological effects.
    OBJECTIVE: To observe the therapeutic effect of hTERT-transfected bone marrow mesenchymal stem cells transplantation in diabetic rats.
    METHODS: Bone marrow mesenchymal stem cells from Sprague-Dawley rats were cultured in vitro and transfected with retrovirus PLXSN carrying hTERT. RT-PCR was used to detect the hTERT expression in the bone marrow mesenchymal stem cells before and after transfection. Sixty male Sprague-Dawley rats were selected and equally randomized into four groups: normal control group, transfection group, cell transplantation group, and model group. In the latter three groups, rats were injected with 45 mg/kg chain urea to establish diabetes models, and then injected via the tail vein with 0.2 mL hTERT-transfected bone marrow mesenchymal stem cells, 0.2 mL bone marrow mesenchymal stem cells, and 0.2 mL normal saline, respectively.
    RESULTS AND CONCLUSION: At 48 hours after hTERT transfection, the expression of hTERT mRNA was detected in the bone marrow mesenchymal stem cells, and mainly concentrated in the nuclei. At 14 days after transfection, the fasting glucose level in the model group was higher than that in the normal control group
    (P < 0.05). However, compared with the model group, the fasting glucose levels in the transfection and cell 
    transplantation groups were significantly decreased (P < 0.05); compared with the cell transplantation group, the fasting glucose level in the transfection group was also significantly decreased (P < 0.05), which was similar to that in the normal control group (P > 0.05). These findings indicate that the transplantation of hTERT-transfected bone marrow mesenchymal stem cells is effective in the treatment of diabetic rats.


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    Allogeneic hematopoietic stem cell transplantation for severe aplastic anemia
    Xi Rui, Bai Hai, Wang Cun-bang
    2015, 19 (6):  912.  doi: 10.3969/j.issn.2095-4344.2015.06.015
    Abstract ( 527 )   PDF (559KB) ( 1583 )   Save

    BACKGROUND: In recent years, with the development of hematopoietic stem cell transplantation technique and the use of immunosuppressants, the therapeutic effects on severe aplastic anemia have been improved significantly. Especially relative HLA-identical matching allogeneic hematopoietic stem cell transplantation has achieved a high cure rate.
    OBJECTIVE: To explore the feasibility of allogeneic hematopoietic stem cell transplantation for the treatment of severe aplastic anemia.
    METHODS: From 2009 to 2011, 20 patients with severe aplastic anemia received fludarabine, cyclophosphamide and antithymocyte globilin as preconditioning before allogeneic hematopoietic stem cell transplantation from 12 matched and 8 mismatched donors. Except one case undergoing unrelated peripheral blood stem cell transplantation, grafts were from mobilized peripheral blood and bone marrow in all cases. Graft versus host disease prophylaxis consisted of cyclosporine-A and short-course methotrexate in the HLA-identical patients as well as cyclosporine, methotrexate, and short-course mycophenolate mofetil in HLA-mismatched patients.
    RESULTS AND CONCLUSION: After transplantation, the time to recover the neutrophil count above > 0.5×109/L was median 12.5 days, and the time to recover the platelet count above > 20×109/L was median 18 days. Twenty patients were followed up for 24-60 months. The overall survival rate was 75% (n=15), the event-free survival rate was 70% (n=14). Five cases died. The event-free survival rate were 83% (10/12 patients) for HLA-identical patients and 50% (4/8 patients) for HLA-mismatched patients. Acute and chronic graft versus host disease was 
    found in 5 of 20 patients, severe bacterial infection in 4 of 20 patients and fungal infections in 3 of 20 patients.  Allogeneic stem cell transplantation is effective in the treatment of severe aplastic anemia, especially for HLA-identical patients.


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    Transfusion strategy to ABO-incompatible grafts in allogeneic hematopoietic stem cell transplantation
    Xu Jin-hua, Li Xiao-feng
    2015, 19 (6):  913-917.  doi: 10.3969/j.issn.2095-4344.2015.06.016
    Abstract ( 685 )   PDF (667KB) ( 1056 )   Save

    BACKGROUND: Hematopoietic stem cell transplantation is an important means for clinical cure of hematologic malignancies, congenital hereditary diseases and autoimmune diseases. Although ABO-incompatibility has no effects on the survival of transplanted hematopoietic stem cells, the transfusion strategy to ABO-incompatible grafts in allogeneic hematopoietic stem cell transplantation is worth studying. 
    OBJECTIVE: To explore the antigen-antibody changes during blood conversion after ABO-incompatible hematopoietic stem cell transplantation as well as transfusion strategies.
    METHODS: Blood grouping, antibody detection, antibody titer determination, cross-match test were employed for antigen-antibody monitoring during blood conversion and pre-transfusion compatibility detection in 24 cases undergoing ABO-incompatible allogeneic hematopoietic stem cell transplantation. Another 30 cases undergoing ABO-compatible allogeneic hematopoietic stem cell transplantation were enrolled as controls to select the appropriate blood.
    RESULTS AND CONCLUSION: All of the 24 ABO-incompatible patients developed the hematopoietic reconstitution after transplantation, but both major and major-minor ABO incompatibility were different from ABO compatibility in the time of erythrocytic recovery (P < 0.05). According to the changes of ABO antigen and antibody during the blood conversion, the patients of major ABO incompatibility were selected the red blood cells of their own type, the patients of minor ABO incompatibility were selected the red blood cells of the blood group from patients to donors gradually, and the patients of major-minor ABO incompatibility were selected the red blood cells from O-type blood to donor’s type gradually. None of the 24 recipients presented hemolytic reaction during transplantation and after transfusion. Therefore, the transfusion strategy to ABO-incompatible grafts in allogeneic hematopoietic stem cell transplantation is dynamically varied according to the changes of patient’s ABO antigen and antibody, and evaluating the recovery of erythropoietic system can guide blood component selection, avoid hemolytic transfusion reaction, and insure the safety of hematopoietic stem cell transplantation.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Transplantation of basic fibroblast growth factor-transfected bone marrow mesenchymal stem cells in the treatment of pulmonary hypertension
    Song Yan-feng, Cao Jie
    2015, 19 (6):  918-922.  doi: 10.3969/j.issn.2095-4344.2015.06.017
    Abstract ( 286 )   PDF (707KB) ( 591 )   Save

    BACKGROUND: Currently, emerging stem cell therapy and gene modification technology have the potential to get a unique effect in the treatment of pulmonary hypertension.
    OBJECTIVE: To investigate the effects of transplantation of basic fibroblast growth factor-transfected bone marrow mesenchymal stem cells on the hemodynamic changes of pulmonary hypertension rats.
    METHODS: Bone marrow mesenchymal stem cells from male Sprague-Dawley rats aged 3 weeks were cultured and purified in vitro, and then transfected with adenovirus-medicated basic fibroblast growth factor. Sixty Sprague-Dawley rats were enrolled to prepare pulmonary hypertension models through intraperitoneal injection
    of 50 mg/kg monocrotaline and then randomly assigned into three groups: model group treated with transplantation of 1 mL L-DMEM via the jugular vein, cell transplantation group treated with transplantation of 1 mL untransfected bone marrow mesenchymal stem cell suspension, and transfection group treated with transplantation of 1 mL bone marrow mesenchymal stem cell suspension transfected with basic fibroblast growth factor.
    RESULTS AND CONCLUSION: After 3 weeks of treatment, there were no differences in the arterial blood pressure of the three groups (P > 0.05); however, the systolic pressure of the pulmonary artery and mean pulmonary arterial pressure were significantly lower in the transfection group than the model group and cell transplantation group
    (P < 0.05). Hypertrophy index of the right ventricle had no difference among the three groups (P > 0.05). The level of plasma endothelin 1 was significantly lower in the transfection group than the model group and cell transplantation group (P < 0.05). Experimental findings suggest that the transplantation of basic fibroblast growth factor-transfected bone marrow mesenchymal stem cells can improve the hemodynamic levels in pulmonary blood vessels of pulmonary hypertension rats to protect vascular endothelial cells and antagonize vascular contraction.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Umbilical cord blood mesenchymal stem cells carrying human telomerase reverse transcriptase for pulmonary arterial hypertension
    Xu Ying
    2015, 19 (6):  923-927.  doi: 10.3969/j.issn.2095-4344.2015.06.018
    Abstract ( 338 )   PDF (771KB) ( 512 )   Save

    BACKGROUND: To protect the pulmonary vascular endothelial cells in the body is an important part to reduce pulmonary circulation pressure and prevent pulmonary hypertension.
    OBJECTIVE: To observe the therapeutic efficacy of umbilical cord blood mesenchymal stem cell transplantation carrying human telomerase reverse transcriptase (hTERT) in the treatment of pulmonary hypertension in rats.
    METHODS: Umbilical cord blood mesenchymal stem cells were cultured, purified and transfected with adenovirus carrying hTERT gene. Sixty Sprague-Dawley male rats were randomly divided into model group, blank adenovirus group, adenoviral delivery group, with 20 rats in each group. Then, the rats were respectively injected via the jugular vein with 1 mL L-DBEB, 1 mL umbilical cord blood mesenchymal stem cell suspension (1.5×1010/L), and 1 mL hTERT-transfected umbilical cord blood mesenchymal stem cell suspension (1.5×1010/L) after models of pulmonary hypertension were established via intraperitoneal injection of monocrotaline. After 21 days of transplantation, hemodynamic changes, plasma endothelin 1 levels and the hypertrophy index of the right ventricle were detected.
    RESULTS AND CONCLUSION: There was no difference in arterial blood pressure among the three groups
    (P < 0.05). In the adenoviral delivery group, the systolic pressure of the pulmonary artery, mean pulmonary artery pressure and plasma endothelin 1 level decreased significantly as compared with the model group, blank adenovirus group (P < 0.05); but no difference was found in the hypertrophy index of the right ventricle (P > 0.05). These findings indicate that umbilical cord blood mesenchymal stem cell transplantation carrying hTERT gene can improve the hemodynamic abnormalities in the body and also protect vascular endothelial cells in the body.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Mechanism of bone marrow mesenchymal stem cells transplantation in the treatment of limb ischemia
    Bai Chao, Yang Kun, Li Xin-xi, Wang Yang, Tian Ye, Luo Jun
    2015, 19 (6):  928-933.  doi: 10.3969/j.issn.2095-4344.2015.06.019
    Abstract ( 336 )   PDF (1703KB) ( 430 )   Save

    BACKGROUND: Bone marrow stem cell transplantation has good achievements in the treatment of lower limb ischemic disease, but it mechanism of action is still unclear.
    OBJECTIVE: To explore the mechanism of bone marrow mesenchymal stem cell transplantation for treatment of limb ischemia in Sprague-Dawley rats.
    METHODS: The abdominal aorta, iliac arteries and lumbar arteries below the renal artery were ligated to prepare hind limb ischemia models in female Sprague-Dawley rats. Bone marrow mesenchymal stem cells from male Sprague-Dawley rats were amplified, purified and injected into the rectus femoris of the ischemic right hind limb in female rat models; in the control group, equal volume of normal saline was injected. After transplantation 2, 4, 6 weeks, hematoxylin-eosin staining of the right rectus femoris, immunohistochemical staining of vascular endothelial growth factor and SRY immunohistochemical staining were performed.
    RESULTS AND CONCLUSION: After operation 2, 4, 6 weeks, the capillary count and the number of cells
    positive for vascular endothelial growth factor in the transplantation group were significantly higher than those in the control group (P < 0.01). SRY immunohistochemical staining showed positive cells appeared at the capillary wall, which scattered in the muscle tissue in the transplantation group. These findings indicate that the local injection of bone marrow mesenchymal stem cells can improve the blood supply of ischemic hind limbs in Sprague-Dawley rats. Bone marrow mesenchymal stem cells as paracrine cells can prompt the neovascularization of ischemic limbs in rats by increasing the secretion of vascular endothelial growth factor.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Co-transplantation of HLA-matched limbal stem cells and amniotic membrane for treatment of pterygium
    Yang Jie, Zhang Jin-sha, Ying Feng
    2015, 19 (6):  934-939.  doi: 10.3969/j.issn.2095-4344.2015.06.020
    Abstract ( 358 )   PDF (906KB) ( 504 )   Save

    BACKGROUND: Co-transplantation of HLA-matched limbal stem cells and amniotic membrane is a new concept for the treatment of pterygium, which is characterized as few complications, fast recovery, and low relapse rate. This treatment has been widely used because of reduced rejections.
    OBJECTIVE: To investigate the therapeutic effect of HLA-matched limbal stem cells and amniotic membrane co-transplantation in the treatment of pterygium.
    METHODS: Forty-seven patients with pterygium (47 eyes) who underwent the co-transplantation of HLA-matched limbal stem cells and amniotic membrane from March 1, 2013 to April 30, 2014 were enrolled as test group. Another 40 patients with pterygium (47 eyes) who received traditional surgical method acted as control group. Therapeutic effectiveness and relapse were compared between the two groups.
    RESULTS AND CONCLUSION: The 47 cases in the test group were successfully treated with no complications and rejections, and only one case suffered from incision infection but discharged from hospital after symptomatic treatment. After treatment, pterygium relapsed in 2 of 47 eyes in the test group and 15 of 47 eyes in the control group, and the relapse rates were 4.3% and 31.9%, respectively. Results from this study show that the co-transplantation of HLA-matched limbal stem cells and amniotic membrane for treatment of pterygium has fewer complications and lower relapse rate, which is an effective method for the treatment of pterygium.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    C57BL/6 mouse bone marrow monocytes: isolation, cultivation, purification and differentiation into osteoclasts
    Zhou Long, Chen Xi, Luo Zong-ping, Yang Hui-lin, He Fan
    2015, 19 (6):  940-944.  doi: 10.3969/j.issn.2095-4344.2015.06.021
    Abstract ( 1591 )   PDF (3885KB) ( 4060 )   Save

    BACKGROUND: Isolation and extraction of bone marrow monocytes is mostly realized via osteoclast differentiation induced by RAW264.7 cells as reported at home and abroad.
    OBJECTIVE: To explore a new method for the isolation, culture, purification and identification of C57BL/6 mouse bone marrow monocytes and to observe the growth features and osteoclast differentiation of mouse bone marrow monocytes in vitro.
    METHODS: The femurs and tibias of C57BL/6 mice were aseptically removed to extract bone marrow cells that were cultured overnight (> 16 hours). During the extraction process, erythrocyte lysate was used to remove red blood cells. At day 2, suspension cells were isolated and cultured with the medium containing macrophage colony-stimulating factor to harvest adhered mouse bone marrow monocytes. The medium was changed to purify and amplify the mouse bone marrow monocytes. Cell morphology was observed, the growth curve was tested and using flow cytometry, the cell surface antigen of primary mouse bone marrow monocytes was detected. Macrophage colony-stimulating factor and receptor activator of nuclear factor-κB ligand were added to 
    differentiate the cells into osteoclasts.   
    RESULTS AND CONCLUSION: The newly separated mouse bone marrow monocytes were circular and feelers were extended from both ends. After 5 days of culture, the cells were oval-shaped with more obvious feelers, and cell proliferation relied on macrophage colony-stimulating factor. Under the flow cytometry, isolated mouse bone marrow monocytes had high purity and could be induced to differentiate into osteoclasts. It is effective to isolate mouse bone marrow monocytes that grow stably by vigorously promoting the proliferation of monocytes by using different adherent abilities of mesenchymal stem cells and monocytes as well as macrophage colony-stimulating factor. Cultured mouse bone marrow monocytes are phenotypically stable and can be used for further research.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Ganglioside effect on Nogo-A expression of rat oligodendrocytes in vitro after carbon monoxide poisoning
    Wang Xiao-hong, Wang Hong, Che Ju-hua, Wang Su-ping, Wang Tao, Zhu Yan-ling
    2015, 19 (6):  945-949.  doi: 10.3969/j.issn.2095-4344.2015.06.022
    Abstract ( 285 )   PDF (772KB) ( 749 )   Save

    BACKGROUND: Nogo-A protein is speculated to have close relationship to delayed encephalopathy after carbon monoxide poisoning because it is a kind of neurite growth inhibitor expressing in oligodendrocytes. Monosialotetrahexosylganglioside can improve nerve damage after carbon monoxide poisoning, but no reports is concerned about whether the neuroprotective effect of ganglioside is related to Nogo-A protein.
    OBJECTIVE: To investigate the protective mechanism of ganglioside on nerve cells after carbon monoxide poisoning from the perspective of Nogo-A in oligodendrocytes.
    METHODS: Rat oligodendrocytes cultured in vitro were divided into three groups: control, carbon monoxide and monosialotetrahexosylganglioside groups. Carbon monoxide and monosialotetrahexosylganglioside groups were cultured in an airtight box containing 1% carbon monoxide. 5 mg/L monosialotetrahexosylganglioside was added into the culture medium of monosialotetrahexosylganglioside group in advance. The expression of Nogo-A mRNA and protein at 6, 24, 48 hours were detected by RT-PCR and immunohistochemistry method, respectively.
    RESULTS AND CONCLUSION: The integrated absorbance values of Nogo-A mRNA and cumulative  
    absorbance values of Nogo-A protein in the carbon monoxide group at 6, 24 and 48 hours were significantly higher than those in the control group (P < 0.05). At 24 hours after carbon monoxide treatment, the integrated absorbance value and cumulative absorbance value of Nogo-A were both higher than those in the control group (P < 0.05), but lower than those in the carbon monoxide group (P < 0.05). The integrated absorbance values of Nogo-A mRNA was significantly associated with the cumulative absorbance values of Nogo-A protein (r=0.95). These findings indicate that carbon monoxide can activate oligodendrocytes, and raise the transcription and translation levels of Nogo-A. The increase expression of Nogo-A protein was due to the high level of Nogo-A mRNA. The protective mechanism of ganglioside on nerve cells after carbon monoxide poisoning is related to inhibition of Nogo-A expression in oligodendrocytes.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Identification of novel HLA alleles: HLA-A*24:233 and HLA-A*26:89
    Liu Xiao-hua, Chi Xiao-yun, Jiao Shu-xian
    2015, 19 (6):  950-954.  doi: 10.3969/j.issn.2095-4344.2015.06.023
    Abstract ( 438 )   PDF (765KB) ( 1186 )   Save

    BACKGROUND: The discovery of novel HLA alleles is accelerated by development of molecular biology and applications of numerous new technologies. These new findings not only rich HLA family, but also find a breakthrough point for the study of genetic superiority or disappearance of national gene.
    OBJECTIVE: To identify two novel HLA-A alleles and to analysis their nucleotide sequences.
    METHODS: The two samples from two volunteers of Chinese Marrow Donor Program were detected using PCR-SBT and GSSP methods. The HLA-A locus in the two samples were both abnormal genes, and the nucleotide sequence differences were analyzed.
    RESULTS AND CONCLUSION: The sequences of the samples were different from all alleles in the HLA databases. Sample 1 was found to be different from the closet matching allele A*24:02:01 in one nucleotide substitutions, 360 G > C in exon 3, resulting in amino acid changed from glutamine to histidine at codon 96; and sample 2 differed from A*26:01:01 in one nucleotide substitution, 97 T > C in exon 2, resulting in amino acid changed from tyrosine to histidine at codon 9. The novel alleles were identified and assigned the name HLA-A*24:233 and HLA-A*26:89 officially by the WHO Nomenclature Committee.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Reduced-intensity conditioning regimen in HLA-haploidentical hematopoietic stem cell transplantation
    Yang Ting, Jiang Ming
    2015, 19 (6):  955-961.  doi: 10.3969/j.issn.2095-4344.2015.06.024
    Abstract ( 402 )   PDF (801KB) ( 1170 )   Save

    BACKGROUND: Reduced-intensity conditioning allogeneic hematopoietic stem cell transplantation (RIC-allo-HSCT) is proved being one of the effective methods to cure hematologic malignancies recently, which has been used more and more in patients with matched sibling or matched unrelated donor year by year. It is more suitable for elderly patients or younger patients combined with any organ dysfunction or complications. However, matched sibling and matched unrelated donors are not easy to be obtained for RIC-allo-HSCT. While HLA-haploidentical donor can be quickly found in family members for the patients who need receiving RIC-allo-HSCT. Fewer papers for reduced-intensity conditioning haploidentical hematopoietic stem cell transplantation (RIC-haplo-HSCT) have been reported in the world, and none in China, so the review for RIC-haplo-HSCT is necessary.
    OBJECTIVE: To reveiw the application of RIC-haplo-HSCT and its prospect.
    METHODS: Using “nonmyeloablative conditioning, reduced intensity conditioning, HLA-haploidentical, hematopoietic stem cell transplantation” as key words, we retrieved Wanfang, CNKI and PubMed databases, and foreign language search platform (1997-2014) by computer for literatures about RIC-haplo-HSCT. According to the inclusion and exclusion criteria, 25 articles in English were selected for our review ultimately.
    RESULTS AND CONCLUSION: This review shows that RIC-allo-HSCT with matched sibling and matched unrelated donor is widely used and has a better result increasingly. RIC-haplo-HSCT is carried out relatively late and less, and its engraftment, infection, transplant-related mortality, graft-versus-host disease, long-term disease-free survival and overall survival in the early period is a bit weak, but overall the situation has been recently improved significantly. Currently RIC-haplo-HSCT is feasible, especially for patients lack of matched sibling donor and matched unrelate donor, and HLA haploidentical donor becomes the most potential source of hematopoietic stem cells. RIC-haplo-HSCT retains strong graft-versus-leukemia effect, and is easy to look for donor, as well as there are sufficient cells for subsequent treatments such as donor lymphocyte infusion, which through a graft-versus-leukemia effect can eliminate the patient’s malignant cells, especially for elderly patients and younger patients combined with any organ dysfunction or complications. However, due to the relative short time to carry out RIC-haplo-HSCT, how to choice optimal RIC regimen and optimal opportunity and how to reduce transplant-related mortality, graft-versus-host disease and relapse rate require further in-depth studies.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Stem cell marker LGR5: a new target for cancer therapy
    Gao Fei, Wei Yan-cai, Yang Chen
    2015, 19 (6):  962-968.  doi: 10.3969/j.issn.2095-4344.2015.06.025
    Abstract ( 929 )   PDF (665KB) ( 3189 )   Save

    BACKGROUND: Recent studies have shown that cancer stem cells play a key role in the development of tumors, therefore, the research about cancer stem cells’ markers can deepen the understanding of the development and clinical diagnosis of the tumor.
    OBJECTIVE: To review the research progression of stem cell marker LGR5.
    METHODS: The first author retrieved PubMed database and Wanfang database for papers regarding LGR5 and stem cell/cancer stem cell published between January 1998 and December 2014 using the key Words “LGR5, stem cell, cancer stem cell” in English and Chinese, respectively. A total of 178 papers were initially retrieved. After 123 papers with independent objective and out-of-date contents were excluded, 55 papers were suitable for final analysis.
    RESULTS AND CONCLUSION: LGR5 is the surface marker of intestinal, stomach, hair follicle stem cells, which has a great relationship with occurrence, development and prognosis of colorectal cancer, stomach cancer, lung cancer, ovarian cancer, liver cancer, basal cell carcinoma. As a candidate marker of cancer stem cells, LGR5 can be the new treatment target. Studies have shown that R-spondins (RSPOs) is a high affinity ligand of LGR5. They participate in the Wnt signaling pathway, regulating cell proliferation and differentiation.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Induced differentiation of adipose-derived stem cells
    Zhao Na
    2015, 19 (6):  969-975.  doi: 10.3969/j.issn.2095-4344.2015.06.026
    Abstract ( 673 )   PDF (895KB) ( 1219 )   Save

    BACKGROUND: Adipose-derived stem cells are pluripotent stem cells developed from the mesoderm, which can differentiate into different lineages induced by specific growth factors and under certain environmental conditions.
    OBJECTIVE: To describe the induced differentiation and identification of adipose-derived stem cells in detail.
    METHODS: A computer-based search of Wanfang and PubMed databases was performed for relevant articles published from 2005 to 2014 using the keywords of “adipose derived stem cells, induced, differentiation” in Chinese and English, respectively. According to inclusion and exclusion criteria, 37 articles were selected in result analysis.
    RESULTS AND CONCLUSION: Adipose-derived stem cells can differentiate into chondrocytes under the induction of ascorbic acid, insulin, dexamethasone, and transforming growth factor β. Recipe for adipogenic induction medium consists of 3-isobutyl-1-methylxanthine (IBMX), insulin, dexamethasone, indomethacin; and commonly used inducers for osteogenic differentiation include dexamethasone or vitamin D3, ascorbic acid, β-glycerophosphate. Basic fibroblast growth factor, epidermal growth factor and vitamin B27 may be combined to induce the differentiation of adipose-derived stem cells into neurons. 5-Azacytidine acts as a commonly used factor for inducing the differentiation of adipose-derived stem cells into cardiomyocytes. Combination of vascular endothelial growth factor and basic fibroblast growth factor can induce adipose-derived stem cells to differentiate into vascular endothelial cells. With the rapid development of molecular biology and cell biology, research on the differentiation of adipose-derived stem cells will be more in-depth. Based on the current observation of  adipose-derived stem cell differentiation, internal molecular mechanism as well as genes and proteins for regulation of adipose-stem cell plasticity should be explored in depth.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Stem cells and stem cell therapy for diabetes mellitus: Chinese clinical trial registration information analysis
    Liu Hong-juan
    2015, 19 (6):  975-979.  doi: 10.3969/j.issn.2095-4344.2015.06.027
    Abstract ( 538 )   PDF (704KB) ( 793 )   Save

    BACKGROUND: The Chinese Clinicaltrial Register publishes the study design information and internationally harmonized registration number, reviews study design, and randomly assigns in order to protect the quality of registration.
    OBJECTIVE: To analyze the current situation of stem cells and stem cell therapy for diabetes mellitus in Chinese Clinical Trial Registry.
    METHODS: We searched the Chinese Clinical Trial Register (2008-2014) for stem cell research, and summarized these studies from the aspects of type of disease, study type, registration date, registration units, geographical distribution. Then, clinical trials about stem cells in the Chinese Clinical Trial Register were further analyzed.
    RESULTS AND CONCLUSION: There are 82 studies about stem cells, which mainly focus on blood disorders (32/39.0%), neurological disorders (20/24.4%), liver (9/11.0%), diabetes (5/6.1%). The registration date is mainly in 2012, and the main registration units are General Hospital of Armed Police Forces, Peking University People’s Hospital and the First Affiliated Hospital of Zhejiang University, which are mainly in Beijing and Zhejiang Province.There are five clinical trials about stem cell therapy for diabetes mellitus, which are umbilical cord mesenchymal stem cell transplantation for diabetes from the General Hospital of Armed Police Forces, therapeutic efficacy and safety of mesenchymal stem cell transplantation for diabetes from Xinqiao Hospital, and autologous bone marrow stem cell transplantation for the treatment of diabetes from the 452nd Hospital of Chinese PLA. There are no enough trails about stem cells and stem cell therapy for diabetes in the Chinese Clinical Trial Register, and to improve clinical trial registration number and specification is the future direction of development.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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    Hematopoietic stem cell transplantation: psychological characteristics and psychological support in recipients
    Zhao Yan-jie
    2015, 19 (6):  980-984.  doi: 10.3969/j.issn.2095-4344.2015.06.028
    Abstract ( 428 )   PDF (667KB) ( 527 )   Save

    BACKGROUND: Hematopoietic stem cell transplantation is the main treatment for leukemia, lymphoma and other blood diseases, but there are various negative factors during the transplantation process that have important implications for the success of hematopoietic stem cell transplantation.
    OBJECTIVE: To analyze the psychological characteristics of patients undergoing hematopoietic stem cell transplantation and to focus on the implementation effects of psychological intervention.
    METHODS: From January 2012 to December 2013, totally 92 patients were admitted at the Hematopoietic Stem Cell Transplantation Center, the majority of whom had received autologous peripheral blood stem cell transplantation. Fifty-five of 92 patients were subjected to allogeneic stem cell transplantation, including 48 cases of relative sources and 7 of unrelated peripheral blood stem cell transplantation. Bone marrow suppression and composite grafting were carried out in some patients. According to the characteristics of negative factors at the different stages of stem cell transplantation, targeted interventional measures were performed, including psychological supports, prevention, observation and treatment of complications, and whole environmental protection programs.
    RESULTS AND CONCLUSION: Hematopoietic stem cell transplantation was successfully implemented in all patients who had good compliance behaviors (medication, diet, and daily schedule), and had no the following adverse events: psychological stress, out of emotional control, destroying objects. No significant difference was found in the incidence of complications, the incidence of adverse events, and patient satisfaction rate during 2012-2013 (P > 0.05). Because the hematopoietic stem cell transplantation has strong specificity, patients need to strictly comply with the treatment path, stay long in laminar flow wards longer, and bear a greater psychological and physiological burden, whose behaviors are severely restricted. We should strictly implement aseptic standards, strengthen ward management and provide good guidance and support for patients, so as to reduce post-transplantation complications and ensure the successful completion of hematopoietic stem cell transplantation.


    中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程


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