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    07 May 2013, Volume 17 Issue 19 Previous Issue    Next Issue
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    Effect of insulin-like growth factor-1 on chondrogenic differentiation of bone marrow mesenchymal stem cells and expression of matrix metalloproteinase
    Wu Bo, Ma Xu, Zhu Da-mu, Liu Su-yuan, Wang Jing-xu, Zhang Yi, Fu Ai-min, Pan Liang
    2013, 17 (19):  3421-3429.  doi: 10.3969/j.issn.2095-4344.2013.19.001
    Abstract ( 300 )   PDF (2440KB) ( 453 )   Save

    BACKGROUND: Studies have shown that insulin-like growth factor-1 serves as a helper factor and is combined combines with other factors to promote the differentiation of bone marrow mesenchymal stem
    cells into chondrocytes. However, whether insulin-like growth factor-1 alone could promote the secretion of cartilage specific collagen remains controversial, and its effect on cell proliferation and stability of cartilage collagenfiber has been rarely reported.
    OBJECTIVE: To investigate the effect of insulin-like growth factor-1 on chondrogenic differentiation and matrix metalloproteinase expression of bone marrow mesenchymal stem cells.
    METHODS: The expression vector carrying complete coding sequence of insulin-like growth factor-1 was constructed, and stably transfected to rat bone marrow mesenchymal stem cells, serving as insulin-like growth factor-1 stable transfection group. Meanwhile, the non-transfection group was taken as the control.
    RESULTS AND CONCLUSION: The 3-(4,5)-dimethylthiahiazo-2-yl-3,5-di-phenytetrazoliumromide assay showed that, insulin-like growth factor-1 stable expressing bone marrow mesenchymal stem cells was successfully established, and cell proliferation was significantly increased after 4 days of transfection (P < 0.05). Reverse transcription-polymerase chain reaction, western blot analysis and immunocytochemistry detection showed that, the mRNA and protein levels of insulin-like growth factor-1 and collagen type Ⅱ were significantly increased in the stable transfection group (P < 0.01), while mRNA levels of matrix metalloproteinase-1, -2 and -3 were significantly decreased compared with the non-transfection group (P < 0.01). Experimental findings confirm that, insulin-like growth factor-1 alone can promote the proliferation of bone marrow mesenchymal stem cells as well as chondrogenic differentiation, and maintain the stability of collagen fibers.

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    In vitro rapid culture system to induce the adipogenic differentiation of rat bone marrow mesenchymal stem cells
    Shi Xiao-qing, Hua Xian-liang, Wen Guan-mei
    2013, 17 (19):  3430-3436.  doi: 10.3969/j.issn.2095-4344.2013.19.002
    Abstract ( 685 )   PDF (2802KB) ( 1190 )   Save

    BACKGROUND: The commonly used adipogenic irritants consist of insulin, dexamethasone, 3-isobutyl-1-methylxanthine and indomethacin. The system is not conducive to the study of adipogenesis inhibitory effect due to the disadvantages of multi-processing factors, long induction period and great cytotoxicity. 
    OBJECTIVE: To develop a rapid culture method to induce adipogenic differentiation of rat bone marrow mesenchymal stem cells.
    METHODS: Rat whole bone marrow cells were primary cultured and passaged with trypsin digestion method. The homogeneous mesenchymal stem cells were enriched, and adipogenic differentiation of rat bone marrow mesenchymal stem cells were in vitro induced with thiazolidinediones (rosiglitazone and pioglitazone), the agonists of peroxisome proliferator-activated receptor γ. Glucose-free, low glucose and high glucose Dulbecco's modified Eagle's media were established, and the classic adipogenic irritants were as the positive control. Morphological observation and oil red O staining were performed to observe the differentiated cells at different time points. 
    RESULTS AND CONCLUSION: Compared with the classic adipogenic irritants, the rosiglitazone and pioglitazone could induce the rat bone marrow mesenchymal stem cells to differentiate into adipocytes, and accumulations of lipid droplets or lipid vesicles and oil red O staining positive cells could be observed after induced with pioglitazone for 48 hours and rosiglitazone for 72 hours. The optional concentration of pioglitazone and rosiglitazone for adipogenic induction was 0.125 mmol/L and 10 μmol/L, respectively. High glucose could enhance the adipogenic differentiation of rat bone marrow mesenchymal stem cells. The culture system with the adipogenic irritants of pioglitazone and rosiglitazone under the high glucose environment can rapidly induce the rat bone marrow mesenchymal stem cells to differentiate into adipocytes.

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    Bone marrow mesenchymal stem cells cultured in vitro and chemokine receptor CXCR4 expression
    Yu Gui-ping, Shen Zhen-ya, Chen Guo-qiang, Yu Yun-sheng, Guo Shi-qiang
    2013, 17 (19):  3437-3442.  doi: 10.3969/j.issn.2095-4344.2013.19.003
    Abstract ( 340 )   PDF (1473KB) ( 297 )   Save

    BACKGROUND: Experiments have demonstrated that the expression level of CXCR4 on bone marrow mesenchymal stem cells determines cell homing to targeted tissue and subsequent angiogenesis.
    OBJECTIVE: To analyze the isolation, culture, identification and multi-differentiation potential of bone marrow mesenchymal stem cells and investigate the significance of chemokine receptor CXCR4 expression on bone marrow mesenchymal stem cells in promotion of angiogenesis.
    METHODS: Under sterile condition, bone marrow mesenchymal stem cells were isolated, cultured and purified by the while bone marrow adherence method. Cell apoptosis in vitro, CXCR4 protein expression on the bone marrow mesenchymal stem cells were detected, and cell cycle was analyzed.
    RESULTS AND CONCLUSION: The isolated bone marrow mesenchymal stem cells exhibited uniform morphology. After passage, cells were spindle-shaped. Cells began to grow rapidly at about 4 days and grew stably 1 week later. Flow cytometry results showed increased CXCR4 expression on bone marrow mesenchymal stem cells. These findings suggest that bone marrow mesenchymal stem cells were successfully isolated, CXCR4 protein was highly expressed on cell surface after in vitro culture, and increased CXCR4 expression will provide theoretical evidence for bone marrow mesenchymal stem cell transplantation in promotion of angiogenesis and treatment of lower limb ischemic diseases in the clinic.

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    Bone marrow mesenchymal stem cells intervene maturation and differentiation of dendritic cells in aplastic anemia patients
    Zhang Le-qin, Xiao Yang, Jiang Zu-jun, Xiao Hao-wen, Li Li, Pang Yan
    2013, 17 (19):  3443-3448.  doi: 10.3969/j.issn.2095-4344.2013.19.004
    Abstract ( 349 )   PDF (814KB) ( 347 )   Save

    BACKGROUND: There are few reports about the influence of bone marrow mesenchymal stem cells on T cell proliferation in aplastic anemia patients in China. Besides, no study is reported in China on the topic that whether bone marrow mesenchymal stem cells affect the T cell proliferation in aplastic anemia patients by dendritic cell regulation. Therefore, its mechanism deserves further investigations.
    OBJECTIVE: To explore effects of human bone marrow mesenchymal stem cells on dendritic cell immune regulation in patients with aplastic anemia.
    METHODS: Human peripheral blood mononuclear cells-derived dendritic cells cultured for 5 days were co-cultured with human bone marrow mesenchymal stem cells at passage 3. Lipopolysaccharide and tumor necrosis factor were added to promote the maturation of dendritic cells. Flow cytometry was used to detect the expression of dendritic cell surface markers before and after coculture of bone marrow mesenchymal stem cells and immature and mature dendritic cells.
    RESULTS AND CONCLUSION: Under the induction of lipopolysaccharide, prior to and following the coculture of immature dendritic cells and bone marrow mesenchymal stem cells, no changes of the expression of CD14, CD1a, CD83 and CD80 were observed (P > 0.05). Prior to and following the coculture of mature dendritic cells and bone marrow mesenchymal stem cells, the expression of CD14, CD1a, CD83 and CD80 was decreased (P < 0.05). Results suggested that bone marrow mesenchymal stem cells can inhibit the development and maturation of dendritic cells derived from monocytes of aplastic anemia patients, and exhibit immunoregulatory effects in patients with aplastic anemia.

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    Differences of human umbilical cord blood-derived mesenchymal stem cells cultured in different media
    Zhao Xia, Lu Xi-jing, Liu Guo-qiang, Xu Min, Xing Jian, Wang Liang, Ding Hui-fang
    2013, 17 (19):  3449-3454.  doi: 10.3969/j.issn.2095-4344.2013.19.005
    Abstract ( 498 )   PDF (711KB) ( 854 )   Save

    BACKGROUND: The umbilical cord blood-derived mesenchymal stem cells are the hot spot in the field of stem cells, and there is no simple, effective culture method for the passage and amplification of umbilical cord blood-derived mesenchymal stem cells.
    OBJECTIVE: To explore a better culture method of human umbilical cord blood-derived mesenchymal stem cells in vitro with different media in the separation of mesenchymal stem cells at a confluent status.
    METHODS: Human umbilical cord blood was sterilely collected from full-term deliveries scheduled for cesarean section. They were assigned randomly into five groups: low-glucose culture medium group, high-glucose culture medium group, α-culture medium group, low-glucose culture medium + stem cell factor group, low-glucose culture medium + human marrow mesenchymal stem cells supernatant group. All culture medium used was Dulbecco’s modIfied Eagle’s medium. The cord blood mononuclear cells were isolated by lymphocyte separation medium. The monocytes of cord blood were inoculated into the culture medium containing 10% fetal bovine serum at 37 ℃ incubator with 0.05 volume fraction of CO2. Quantity and formation of cells were observed with invert microscope, and surface antigenic features were analyzed with flow cytometry.
    RESULTS AND CONCLUSION: (1) Comparison on number of adherent cells and survival rate of mesenchymal stem cells cultured for 48 hours: Number of adherent cells in the low-glucose culture medium + human marrow mesenchymal stem cells supernatant group, and low-glucose culture medium + stem cell factor group were significantly increased (P < 0.05), while the survival rate of cells was also increased compared with low-glucose culture medium group, high-glucose culture medium group and α-culture medium group (P < 0.05). (2) Comparison on growth status of mesenchymal stem cells at different culture time points: Cell proliferation in the low-glucose culture medium + human marrow mesenchymal stem cells supernatant group, and low-glucose culture medium + stem cell factor group was more rapid than that in low-glucose culture medium group, high-glucose culture medium group and α-culture medium group at 3, 6, 9, 12, 15, 18 and 21 days (P < 0.05). There was no significant difference between low-glucose culture medium + human marrow mesenchymal stem cells supernatant group and low-glucose culture medium + stem cell factor group. Experimental findings indicate that, co-culture with low-glucose culture medium + stem cell factor or human marrow mesenchymal stem cells supernatant can promote the in vitro isolation, culture and proliferation of human umbilical cord blood-derived mesenchymal stem cells.

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    In vitro radiosensitivity of brain cancer stem cells in brain glioma
    Zhao Zhong-fu, Fan Rui-tai, Yang Yong, Sun Jian-rui, Hu Xiang, Eileen Shen, Yang Bo
    2013, 17 (19):  3455-3460.  doi: 10.3969/j.issn.2095-4344.2013.19.006
    Abstract ( 398 )   PDF (746KB) ( 641 )   Save

    BACKGROUND: Radiotherapy effect on of brain glioma is not ideal, and there are various possible factors that influence the therapeutic effect.
    OBJECTIVE: To investigate the in vitro radiosensitivity of brain cancer stem cells in brain glioma.
    METHODS: Glioma cells were isolated and seeded into the serum-free medium containing growth factors for culture. Glioma cells from the most active cell site were subcultured to 3-5 generations. Glioma cell vitality was assessed to determine the optimal dose of X-ray radiation.
    RESULTS AND CONCLUSION: Distinct difference in activities of proliferation could be found among cancer stem cells from different sites of glioma. X-ray dosages above 8 Gy had notable killing effect on brain cancer stem cells. Different irradiation dosage had different influence on cancer stem cells.

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    Human umbilical cord blood mesenchymal stem cell transplantation for the treatment of hepatic cirrhosis in rats
    Zhan San-hua, Zhang Lu-feng, Yao Wei-min, Yang Ming-hui, Song Xiao-ling, Jiao Hong-liang
    2013, 17 (19):  3461-3466.  doi: 10.3969/j.issn.2095-4344.2013.19.007
    Abstract ( 396 )   PDF (665KB) ( 500 )   Save

    BACKGROUND: Studies have shown that cord blood mesenchymal stem cells can be induced into hepatocyte-like cells in a specific environment, and the transplanted cells can exercise the normal function of liver cells.
    OBJECTIVE: To establish the rat model of hepatic cirrhosis induced with carbon tetrachloride, and to observe the therapeutic effect of umbilical cord blood mesenchymal stem cell transplantation on a rat model of hepatic cirrhosis.  
    METHODS: Hepatic cirrhosis models were established through carbon tetrachloride inducing, then 20 rat models of hepatic cirrhosis were randomly divided into two groups. The control group was injected with 0.5 mL normal saline via the tail vein; the treatment group was injected with chloromethyl benzamide labeled umbilical cord blood mesenchymal stem cell suspension, and the number of the stem cells was 1×106. After 2 weeks, all animals were sacrificed. Liver tissues were obtained for the histological observation and the venous blood was collected to detected the liver function indicators.
    RESULTS AND CONCLUSION: The liver cells of the hepatic cirrhosis models were loose and cloudy swelling, part of the cells were degenerated and necrosis, the structure of the hepatic lobule was vague, and several pseudolobules with different sizes were formed which meet the diagnostic criteria of hepatic cirrhosis. Compared with the control group, the level of serum albumin in the treatment group was significantly increased (P < 0.05), while the levels of bilirubin and transaminases in the treatment group were significantly decreased (P < 0.05). There were lots of red chloromethyl benzamide labeled umbilical cord blood mesenchymal stem cells in the liver tissue of the treatment group. Human umbilical cord blood mesenchymal stem cells can effectively improve the physiological function of hepatic cirrhosis through tail vein.

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    Bone marrow mesencyhmal stem cell transplantation combined with edaravone for the treatment of cerebral infarction in rats
    Sun Jing-jing, Zhang Peng, Zhou Guo-qing
    2013, 17 (19):  3467-3473.  doi: 10.3969/j.issn.2095-4344.2013.19.008
    Abstract ( 303 )   PDF (747KB) ( 394 )   Save

    BACKGROUND: Edaravone can scavenge free radicals and inhibit lipid peroxidation, which can improve microenvironment injury after central nervous system injury.
    OBJECTIVE: To investigate the effect of bone marrow mesenchymal stem cell transplantation combined with edaravone on the treatment of cerebral infarction in rats.
    METHODS: The models of cerebral infarction were made by middle cerebral artery occlusion. Model rats were randomly divided into control group, stem cell group (bone marrow mesenchymal stem cell transplantation) and combination group (edaravone+bone marrow mesenchymal stem cell transplantation). The concentration of 2.0×106/mL bone marrow mesenchymal stem cell suspension or the concentration of 1 mL cell culture fluid was injected into the rat models through the caudal vein; at the same time, 3 mg/(kg•d) edaravone aqueous solution or normal saline was injected into the rat models through the abdominal cavity, for 5 days. The neurobehavioral scores were determined after 24 hours, 3 days and 1, 2 weeks after modeling. Aquaporin 9 and aquaporin-4 mRNA expressions were determined by reverse transcription-PCR. The rats were sacrificed for neuron and brain tissue around target morphological analysis by hematoxylin-eosin staining under a light microscopy. 
    RESULTS AND CONCLUSION: There was no difference in the neurological deficit scores among the three groups at 24 hour and 3 days after treatment (P > 0.05); while after 2 weeks, the neurological deficit score in the combination group was significantly lower than the stem cell group and control group (P < 0.05-0.01). In the stem cell group, the Aquaporin 9 and aquaporin-4 mRNA expressions were higher than the combination group but lower than the control group (P < 0.05). The number of CM-Dil-positive cells and neurons was higher in the combination group than the stem cell and control groups (P < 0.05). These findings indicate that transplanted bone marrow mesenchymal stem cells can survive and migrate to the peri-infarct region, and differentiate into neuron-like cells. Bone marrow mesencyhmal stem cell transplantation combined with edaravone can significantly improve neurological function of cerebral infarction rats.

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    Human umbilical cord-derived mesenchymal stem cell transplantation for treatment for onset type 1 diabetes mellitus
    Yu Wen-long, Xu Wei, Yu Jiang-su, Wang Li, Gao Hong, Wang Yan-gang
    2013, 17 (19):  3474-3480.  doi: 10.3969/j.issn.2095-4344.2013.19.009
    Abstract ( 364 )   PDF (1755KB) ( 398 )   Save

    BACKGROUND: Mesenchymal stem cells have self-replicating, immune tolerance and tissue repair characteristics. Type 1 diabetes mellitus is an autoimmune disease mainly resulting from islet beta-cell damage. In view of this, mesenchymal stem cells can be considered to prevent and treat type 1 diabetes mellitus.
    OBJECTIVE: To observe the effect of umbilical cord mesenchymal stem cell transplantation on the newly-onset type 1 diabetic mice (NOD mice).
    METHODS: Type 1 diabetes model mice (NOD mice) were selected and divided into control group (Group A, mice without onset were injected with normal saline 1 mL into the tail vein), interventional group (Group B, onset mice were injected with 1 mL stem cells into the tail vein, 1 × 106 cells per mouse), and group without injection of umbilical cord mesenchymal stem cells after onset (Group C, onset mice were injected with normal saline 1 mL into the tail vein). Three months later, blood glucose and daily insulin dose were detected; the number and proportion of CD4+, CD8+T cells and CD4+CD25+ regulatory T cells were determined using a flow cytometry; levels of interleukin-2, interleukin-10 and tumor necrosis factor alpha were detected using enzyme linked immunosorbent assay; and fasting and 2-hour postprandial C-peptide levels were detected using enzyme-linked immunosorbent double antibody sandwich method. Islet morphology and lymphocyte infiltration were observed based on pathological sections. The number and size of the islet α and β cells were determined by using immunohistochemical method.
    RESULTS AND CONCLUSION: (1) Compared with the group C, the immunohistochemical results confirmed that infiltration of lymphocytes in the group B was significantly reduced, the structure of islet α and β cells was more complete and the number of α and β cells was significantly increased and consistent. (2) Compared with the group C, the CD4+ T cell number and the rate of CD4+/CD8+ T cells in the group B were lower (P < 0.05), while the number of CD4+ CD25+ regulatory T cells in the group B was higher (P < 0.01). (3) Compared with the group C, the tumor necrosis factor-α level was significantly lower in the group B, but interleukin-10 level was increased in the group B (P < 0.01). (4) Compared with the group C, the group B had lower blood glucose level and insulin dose, but a higher C-peptide level (P < 0.05). It is indicated that umbilical cord-derived mesenchymal stem cells have a positive effect on the treatment of onset type 1 diabetes mellitus, which can reduce blood glucose level and insulin dose.

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    Effects of intravenous transplantation of human umbilical cord blood mononuclear cells combined with perindopril on inflammatory response of acute myocardial infarction
    Deng Liu-xia, Yu Guo-long, Ai Qi, Yuan Chun-ju
    2013, 17 (19):  3481-3487.  doi: 10.3969/j.issn.2095-4344.2013.19.010
    Abstract ( 304 )   PDF (2147KB) ( 381 )   Save

    BACKGROUND: A recent study has indicated that angiotensin-converting enzyme inhibitor, perindopril, combined with transplantation of bone marrow-derived mesenchymal stem cells can reduce inflammatory response in the injured myocardium associated with enhanced improvement of cardiac function in an animal model of acute myocardial infarction. 
    OBJECTIVE: To observe the effects of intravenous transplantation of human umbilical cord blood mononuclear cells combined with perindopril on the inflammatory responses and pro-inflammatory cytokine interleukin-6 expression as well as the cardiac function in rabbits with acute myocardial infarction, and to investigate the possible protective mechanism of the combination treatment for acute myocardial infarction.
    METHODS: The human umbilical cord blood mononuclear cells were obtained from healthy full-term delivery maternal cord blood. Sixty healthy rabbits were selected to establish the models of acute myocardial infarction, and the models were divided into four groups randomly: control group, perindopril group, simple transplantation group and combination group. Five rabbits were selected from each group to detect the cardiac function index of left ventricular ejection fraction and left ventricular fractional shortening with echocardiography at 1, 2 and 4 weeks after treatment. Hematoxylin-eosin staining was performed to observe the myocardial pathological changes and white blood cell count under light microscope. The protein expression of interleukin-6 in myocardial tissue was detected with immunohistochemistry. The number of green fluorescent protein-positive cells was observed under fluorescence microscope.
    RESULTS AND CONCLUSION: Compared with the control group, left ventricular ejection fraction and left ventricular fractional shortening were significantly improved in the perindopril group, simple transplantation group and combination group at 1, 2 and 4 weeks respectively after the treatment (P < 0.05). The improvement of cardiac function index in simple transplantation group was higher than that in the perindopril group and most significantly in the combination group among the three treatment groups (P < 0.05). Compared with the control group, the number of white blood cells and the expression of interleukin-6 were decreased significantly in the perindopril group, simple transplantation group and combination group (P < 0.05). The number of white blood cells and the expression of interleukin-6 were lower in the simple transplantation group than in the perindopril group (P < 0.05), and lowest in the combination group among the three treatment groups (P < 0.05). Green fluorescent protein-positive cells were found to distribute in the peri-myocardial infarction area in the simple transplantation group and combination group at 1, 2 and 4 weeks after treatment, and the number of the green fluorescent protein-positive cells in the combination group was more than that in the simple transplantation group. The findings indicate that the combination of intravenous transplantation of human umbilical cord blood mononuclear cells and perindopril in the treatment of rabbits with acute myocardial infarction can increase the survival rate of transplanted cells, and further enhance the improvement of the heart function. The possible mechanism may be relate to the combination treatment, which can inhibit the local myocardial inflammation response and the expression of pro-inflammatory cytokine, interleukin-6, effectively.

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    Bone marrow mesenchymal stem cell transplantation for the treatment of temporomandibular joint osteoarthrosis
    Yang Xing-hua, Peng Lin, Liu Yun-sheng, Xing Zai-chen, Li Hai-feng, Li Yu-qing, Liu Min
    2013, 17 (19):  3488-3494.  doi: 10.3969/j.issn.2095-4344.2013.19.011
    Abstract ( 372 )   PDF (1972KB) ( 517 )   Save

    BACKGROUND: With the development of stem cell technology, it is possible to repair cartilage injury using tissue engineering technology, and bone marrow mesenchymal stem cells have become the research focus because of their advantages.
    OBJECTIVE: To observe the treatment effect of stem cells on rabbit temporomandibular joint disorders throughinjection of bone marrow mesenchymal stem cells cultured in vitro into a rabbit model of temporomandibular joint disorder.
    METHODS: The bone marrow mesenchymal stem cells were cultured and identified with in vitro whole blood adherent method. Then the cells were amplified in vitro and induced to differentiate into chondrocytes for using. Intraarticular injection of type Ⅱ collagenase was performed to establish the animal model of temporomandibular joint disorder. In the experimental group, intraarticular injection of induced chondrocytes was performed; and in the control group, the rabbits were injected with un-induced cells. The treatment effect was compared between two groups through observing the chewing and tissue sections of the animals.
    RESULTS AND CONCLUSION: A small amount of colony formation could be seen in the separated cells at 7-14 days; and at 20 days, the cells covered the bottom of the bottle basically. The stro-1+ and CD44+ flow cytometry and immunohistochemical determination showed the cells had the characteristics of stem cells; strong positive type Ⅱ collagen immunohistochemical staining of cells could be seen after induced into chondrocytes. Symptoms of unilateral chewing could be observed at 2 weeks after intraarticular injection of type Ⅱ collagenase. After intraarticular injection of bone marrow mesenchymal stem cells induced chondrocytes into the animal models, the unilateral chewing in the experimental group was weaker than that in the control group. Tissue sections showed that the induced chondrocytes could promote the repair of joint injury, and the cartilage and collagen generation in the experimental group was more than that in the control group. Intraarticular injection of bone marrow mesenchymal stem cells induced chondrocytes can promote the healing of rabbit temporomandibular joint osteoarthrosis.

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    Role of transient receptor potential melastatin 7 in the proliferation of human dental pulp stem cells
    Cui Li, Xu Shuai-mei, Wu Bu-ling
    2013, 17 (19):  3495-3502.  doi: 10.3969/j.issn.2095-4344.2013.19.012
    Abstract ( 332 )   PDF (2205KB) ( 443 )   Save

    BACKGROUND: Transient receptor potential melastatin 7 channel is widely distributed in tissues and cells, and it is necessary for cell survival, proliferation and maintenance of magnesium ion balance.
    OBJECTIVE: To investigate the role of transient receptor potential melastatin 7 channel in the proliferation of human dental pulp stem cells.
    METHODS: Human dental pulp stem cells were isolated and cultured by collagenase digestion method, and were exposed for 72 hours to 2-aminoethoxydiphenyl borate (50 and 100 μmol/L), which was widely used as an inhibitor of transient receptor potential melastatin 7. The influences of 2-aminoethoxydiphenyl borate on transient receptor potential melastatin 7 protein level and proliferation of human dental pulp stem cells were detected with western blot assay and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide method, respectively. Specific lentivirus vector was constructed to inhibit the expression of transient receptor potential melastatin 7, and lentivirus was applied to transfect human dental pulp stem cells. Reverse transcription-PCR and western blot for silencing efficacy analysis were also performed. Changes of cell proliferation after specific silencing transient receptor potential melastatin 7 was examined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay at 1, 3, 5, and 7 days after culture.
    RESULTS AND CONCLUSION: The proliferation of human dental pulp stem cells and protein expression of transient receptor potential melastatin 7 were significantly inhibited by 2-aminoethoxydiphenyl borate at 50 and 100 μmol/L (P < 0.01). After specific silencing transient receptor potential melastatin 7, the proliferation capacity of human dental pulp stem cells was significantly decreased at different time poinrs (P < 0.01). Transient receptor potential melastatin 7 plays an important role in maintaining proliferation ability of human dental pulp stem cells.

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    Rat amniotic epithelial cells are induced to differentiate into neural-like stem cells in vitro
    Guo Bing, Xu Jia-jun
    2013, 17 (19):  3503-3507.  doi: 10.3969/j.issn.2095-4344.2013.19.013
    Abstract ( 302 )   PDF (1603KB) ( 394 )   Save

    BACKGROUND: Previous studies have found that Schwann cells, olfactory ensheathing cells, neural stem cells and activated macrophages may repair nerve injuries, but these cells have some deficiencies, such as source restrictions, tumorigenicity, and allograft rejection. Amniotic epithelial cells have no above-mentioned limits, and possess multiple-differentiation potential. After the induction, amniotic epithelial cells may differentiate into cardiomyocyte-like cells, neural stem cells, liver cells, osteoblasts and chondrocytes.
    OBJECTIVE: To culture rat amniotic epithelial cells which can be induced to differentiate into neural-like stem cells.
    METHODS: Rat amniotic epithelial cells were collected from late pregnancy rats using digestion method. Serum-free medium of nerve stem cells was used to induce rat amniotic epithelial cells into neural-like stem cells. Normal and induced cells were identified by immunocytochemistry and reverse transcription-PCR methods.
    RESULTS AND CONCLUSION: The morphological observation showed that amniotic epithelial cells cultured in the conditioned medium presented with cell body retraction and part of nuclei showed refractive enhancement; dendrite- and axon-like structures appeared, and these processes were woven into a mesh and adhered firmly. Immunocytochemistry results showed that the induced amniotic epithelial cells had a slightly stronger expression of Nestin and glial fibrillary acidic protein, while the pluripotent markers SSEA-4 and Vimentin expressions were weakened. Reverse transcription-PCR test showed that the induced amniotic epithelial cells had a higher mRNA expression of Nestin, glial fibrillary acidic protein and microtubule-associated protein, while the mRNA expression of mesodermal smooth muscle cell marker smooth muscle-22α and pluripotent markers Sox-2 and Nanog declined. These findings suggest that cultured rat amniotic epithelial cells can be induced to differentiate into neural-like stem cells.

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    Neural stem cell transplantation for the treatment of rat spinal cord injury in recovery period
    Li Zhe, Shen Li-fang, Wang Guo-sheng, Guo Gang-hua
    2013, 17 (19):  3508-3514.  doi: 10.3969/j.issn.2095-4344.2013.19.014
    Abstract ( 412 )   PDF (891KB) ( 479 )   Save

    BACKGROUND: Studies have found that extracellular signal-regulated kinase can up-regulate the reactive glial cells after spinal cord injury, and the number of phosphorylated extracellular signal-regulated kinase is increased.
    OBJECTIVE: To evaluate the effect of neural stem cell transplantation on motor function recoveryof rats with spinal cord injury in the recovery period, and to explore the focal differentiation and mechanism.
    METHODS: Ninety Sprague Dawley rats were randomly divided into three groups, 30 rats in each group: control group, local transplantation group and intravenous infusion group. Rats in the control group were used to establish the models but did not receive neural stem cell transplantation; rats in the local transplantation group and the intravenous infusion group received neural stem cell transplantation after modeling. Six rats were collected from each group; then Basso, Beattie and Bresnahan score and immunohistochemical staining were performed at 1, 2, 4, 12 and 24 weeks after transplantation.
    RESULTS AND CONCLUSION: After neural stem cell transplantation, Brdu positive cells could be seen in local lesions of local transplantation group and the intravenous infusion group; Basso, Beattie and Bresnahan score at 4 weeks after transplantation in the local transplantation group and the intravenous infusion group was significantly higher than that in the control group; levels of rat spinal cord glial fibrillary acidic protein and extracellular signal-regulated kinase 1/2 were gradually increased and reached peak at 4 weeks after transplantation; at 12 weeks after transplantation, the levels of spinal cord glial fibrillary acidic protein and extracellular signal-regulated kinase 1/2 were decreased (P < 0.05); the level of microtubule-associated protein 2 was increased and reached peak at 4 weeks after transplantation, and gradually decreased after 4 weeks; at 12 weeks after transplantation, there was no significant difference in microtubule-associated protein 2 level, but the microtubule-associated protein 2 level was higher than that in the control group (P < 0.01). After neural stem cell transplantation, the neural stem cells could proliferate and differentiate into neuron and neuroglial cells. There is no significant difference between the two methods. There may be a certain correlation between the glial cells regeneration process and extracellular signal-regulated kinase pathways.

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    Autologous bone marrow cell transplantation combined with hyperbaric oxygen for the treatment of bone nonunion of four limbs
    Zhang Chuan-kai, Shi Yue, Sun Yang, Feng Hui, Liu Ying, Han Bing, Liu Jun-quan
    2013, 17 (19):  3515-3520.  doi: 10.3969/j.issn.2095-4344.2013.19.015
    Abstract ( 308 )   PDF (592KB) ( 395 )   Save

    BACKGROUND: Bone nonunion due to a variety of causes after fracture is a common orthopedic complication. The existing operation therapy cannot be satisfied with the efficacy. Looking for a minimally invasive, safe and effective treatment method has become the research focus of the orthopedic scholars.
    OBJECTIVE: To observe the clinical curative effect of autologous bone marrow cell transplantation combined with hyperbaric oxygen in the treatment of nonunion of four limbs.
    METHODS: Under routine disinfection and local anesthesia, 10-20 mL bone marrow was extracted from patients to separate, condense and prepare bone marrow cell suspension 2-4 mL. The autologous bone marrow cell concentrate was injected to the nonunion site at the multi-punctures under the guidance of positioning of the C-arm X machine. Sterile dressings were performed after local compression for 3-5 minutes. Hyperbaric oxygen therapy was performed after engraftment of bone marrow cells immediately, 10 times as one course. There was an interval of 5 days between the two courses, a total of three courses.
    RESULTS AND CONCLUSION: Of 37 nonunion cases, 36 cases were healed, and the efficacy assessment was excellent in 25 cases, good in eight cases, general in three cases, and poor in one case; the average time of callus formation was (7.22±1.96) weeks, and the average healing time was (7.91±1.79) months. After bone marrow cell implantation, no serious complications occurred. Autologous bone marrow cell transplantation combined with hyperbaric oxygen for the treatment of bone nonunion can promote the healing of nonunion, which is an effective treatment method.

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    Glucocorticoid effects on adult hippocampal neural progenitor cells
    Yu Xiu-jun, Li Yi, Tai Li-wen, Chen Xiang
    2013, 17 (19):  3521-3526.  doi: 10.3969/j.issn.2095-4344.2013.19.016
    Abstract ( 467 )   PDF (632KB) ( 519 )   Save

    BACKGROUND: In vivo studies have shown that the high concentration of glucocorticoids can inhibit the proliferation of rat endogenous neural precursor cells. Neuron-glia antigen 2 proteoglycan-positive neural progenitor cells are the largest proliferating cell population in the mature central nervous system, which are pluripotent cells.
    OBJECTIVE: To investigate the effects of glucocorticoid on the survival and proliferation of the neuron-glia antigen 2 proteoglycan-positive neural progenitor cells from in vitro cultured adult rat hippocampus.
    METHODS: Neuron-glia antigen 2 proteoglycan-positive neural progenitor cells were primary cultured and sub-cultured. The passage 1 cells were treated with dexamethasone with the concentrations of 0, 0.1, 1, 10
    and 100 μmol for 48 hours, and then the cell activities were determined by lactate dehydrogenase assay, the apoptosis was detected by terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling assay, and the proliferation of the cells was identified by 5'-bromodeoxyuridine incorporation method.
    RESULTS AND CONCLUSION: Dexamethasone with the concentrations of 1, 10 and 100 μmol could decrease the number of the neuron-glia antigen 2 proteoglycan-positive neural progenitor cells, increase the number of terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling positive cells, and significantly reduce the number of BrdU positive cells. High concentration of glucocorticoid can decrease the number of the neuron-glia antigen 2 proteoglycan-positive neural progenitor cells by inhibiting the proliferation and inducing the apoptosis.

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    Synapsin expression of endogenous neural stem cell membrane in a mouse model of amyotrophic lateral sclerosis
    Ye Xue, Ma Chun-chao, Yao Yang, Zang Da-wei
    2013, 17 (19):  3527-3532.  doi: 10.3969/j.issn.2095-4344.2013.19.017
    Abstract ( 333 )   PDF (624KB) ( 418 )   Save

    BACKGROUND: Fibroblast growth factor 2 is one of the main neurotrophic factors for nervous system, has been proved to have a role in promoting the differentiation of endogenous neural stem cells.
    OBJECTIVE: To detect the improvement of motor behavior and the proliferation of endogenous neural stem cells, the level of synapsin and the correlation between the differentiation number of endogenous neural stem cells and the level of synapsin in the SOD1G93A G1H transgenic mouse model of amyotrophic lateral sclerosis after fibroblast growth factor 2 administration.
    METHODS: Sixty new born SOD1G93A G1H transgenic mice (mouse models of amyotrophic lateral sclerosis) were divided into amyotrophic lateral sclerosis group and fibroblast growth factor 2 group, 30 mice in each group. Thirty newborn wild B6SJL mice were collected as normal control group. Mice in the fibroblast growth factor 2 group received intraperitoneal injection of fibroblast growth factor 2; the mice in the amyotrophic lateral sclerosis group and the normal control group received intraperitoneal injection of placebo normal saline. The improvement of motor behavior was evaluated with Rotarod test at postnatal 60, 90 and 120 days; immunohistochemistry was used to mark the endogenous neural stem cells and count the synapsin; the correlation between the differentiation number of endogenous neural stem cells and the level of synapsin was evaluated with Spearman statistical method.
    RESULTS AND CONCLUSION: Compared with the amyotrophic lateral sclerosis group, the fibroblast growth factor 2 group showed a statistically significant improvement in the motor behavior, number of endogenous neural stem cells and level of synapsin were significantly increased. There was a negative correlation between the differentiation number of endogenous neural stem cells and level of synapsin. The neuro-protection mechanism of fibroblast growth factor 2 may be associated with the proliferation of endogenous neural stem cells and level of synapsin.

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    Alkaloids of Buyang Huanwu decoction promote the in vitro proliferation of human umbilical cord blood stem cells
    Cai Yong, Lin Jin-li, Bulinbaiyila
    2013, 17 (19):  3533-3537.  doi: 10.3969/j.issn.2095-4344.2013.19.018
    Abstract ( 267 )   PDF (644KB) ( 417 )   Save

    BACKGROUND: Studies have shown that Buyang Huanwu decoction has protection effect on various cells, but the mechanism is unclear. Some studies have speculated that the alkaloids of Buyang Huanwu decoction play a role.
    OBJECTIVE: To observe the effect of alkaloid of Buyang Huanwu decoction on the in vitro proliferation of human umbilical cord blood stem cells.
    METHODS: Fresh umbilical cord blood was obtained from healthy puerperant to prepare the human umbilical cord blood stem cells suspension, then the purified human umbilical cord blood stem cells were seeded into 40 culture dishes for passage. The cells were divided into four groups. The cells in the tetramethylpyrazine group were cultured with 100 g/L tetramethylpyrazine, the cells in the ferulic acid group were cultured with 50 g/L ferulic acid and the cells in the alkaloids group (tetramethylpyrazine+ferulic acid group) were cultured with 100 g/L tetramethylpyrazine and 50 g/L ferulic acid; cells in the control group were continuously cultured with Dulbecco’s modified Eagle’s medium containing fetal bovine serum with the volume fraction of 20%. The proliferation of human umbilical cord blood stem cells were observed after cultured for 2, 4, 6, 8 and 10 days; after cultured for 24 and 72 hours, the ratio of human umbilical cord blood stem cells in S phase was determined by flow cytometry, and after cultured for 10 days, the resting membrane potential changes were recorded with current clamp mode.
    RESULTS AND CONCLUSION: The proliferation of human umbilical cord blood stem cells in the tetramethylpyrazine group and ferulic acid group was not obvious; after cultured for 10 days, the proliferation of human umbilical cord blood stem cells in the alkaloids group was significantly higher than that in the tetramethylpyrazine group, ferulic acid group and control group (P < 0.01). After cultured for 24 and 72 hours in the alkaloids group, the number of human umbilical cord blood stem cells in S phase was increased; the resting membrane potential in the alkaloids group was higher than that in the tetramethylpyrazine group, ferulic acid group and control group (P < 0.01). The results indicate that the alkaloid of Buyang Huanwu decoction can promote the proliferation of human umbilical cord blood stem cells.

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    Adult neural stem cells and the microenvironment
    Wu Ling-feng, Wu Xiao-mu
    2013, 17 (19):  3538-3545.  doi: 10.3969/j.issn.2095-4344.2013.19.019
    Abstract ( 519 )   PDF (568KB) ( 843 )   Save

    BACKGROUND: Adult neural stem cells are widely distributed in the central nervous system, and have self-renewal and differentiation potential, which can be used as endogenous stem cells to repair injured nerve tissues.
    OBJECTIVE: To summarize the research progress of neural stem cells and the microenvironment.
    METHODS: The first author searched PubMed (1989/2012) and CNKI (2001/2012) using the key words of “neural stem cells; microenvironment; regulation” in English and Chinese, respectively. 
    RESULTS AND CONCLUSION: By screening title and abstract contents, papers with original, reliable and comprehensive analysis were selected, and repetitive research and poor quality articles were excluded. There were 379 English papers and 131 Chinese papers. Finally, only 64 papers were included in result analysis. Adult neural stem cells are closely related to the major cellular components of the microenviroment (vessels, endothelial cells, astrocytes and ependymal cells) and the extracellular matrix in which they are embedded, playing an important role in the regulation of adult neural stem cell survival, proliferation, differentiation. At the same time, the differentiation of adult neural stem cells is regulated by genes. It will produce a new direction of nerve tissue repair between the study of adult neural stem cells and the microenvironment.

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    Comparison of mesenchymal stem cells from three different perinatal tissues
    Ju Ya-ping, Zhao Qing-hua
    2013, 17 (19):  3546-3550.  doi: 10.3969/j.issn.2095-4344.2013.19.020
    Abstract ( 800 )   PDF (534KB) ( 582 )   Save

    BACKGROUND: Human perinatal tissue has drawn extensive attention as an excellent resource of mesenchymal stem cells. 
    OBJECTIVE: To compare the different characteristics of three kinds of mesenchymal stem cells from different human perinatal tissues.
    METHODS: The PudMed database was searched for the related articles published from January 2002 to April 2012 with the key words of “mesenchymal stem cells, fetal blood, umbilical cord, placenta”. The most authorized and representative articles related to mesenchymal stromal cells from the fetal blood, umbilical cord and placenta were included.
    RESULTS AND CONCLUSION: More than 248 articles were screened out by computer according to inclusive and exclusive criteria after initial search, 16 documents of which were involved for review. Articles illuminated the isolation methods and biological characteristics of mesenchymal stem cells from the three different human perinatal tissues. Compared with the mesenchymal stem cells from the fetal blood and placenta, the mesenchymal stem cells from the umbilical cord have become the relatively superior sources of mesenchymal stem cells due to the advantages of simple separation method, highs separation rate, high amplified potential, high differentiation potential and low tumorigenicity.

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    Extrinsic factors regulating apoptosis in cancer stem cells
    Jiang Xue-mei, Li Hua
    2013, 17 (19):  3551-3557.  doi: 10.3969/j.issn.2095-4344.2013.19.021
    Abstract ( 316 )   PDF (576KB) ( 376 )   Save

    BACKGROUND: Accumulative evidence shows that cancer stem cells or tumor-initiating cells are key drivers of tumor formation and progression. The conventional treatment modalities are hampered by the strong resistance of these cells. There have been a few studies addressing the therapy of oriented apoptosis of cancer stem cells. 
    OBJECTIVE: To review the extrinsic factors regulating apoptosis in cancer stem cells.
    METHODS: The first author retrieved PubMed database and Wanfang database for papers regarding cancer stem cells and stem cell apoptosis published between January 1990 and December 2011 using the key Words “cancer stem cells, apoptosis, extrinsic factors” in English and Chinese. A total of 120 papers were initially retrieved. After excluding papers with independent objective and out-of-date contents, 50 papers were suitable for final analysis.
    RESULTS AND CONCLUSION: The cancer stem cell theory has significant implications in cancer research. It is a breakthrough not only in our understanding of the behavior of malignancies but also in our ability to develop new therapeutic approaches. The extrinsic factors regulating apoptosis in cancer stem cells provided by the microenvironment include secreted survival factors, adhesion-mediated apoptosis resistance and hypoxic conditions. The potential microenvironment regulating cancer stem cells is a key filed of research and is still in research. Explaining cancer stem cell regulation using various well known mechanisms will be considered in the future study.

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    Stem cells in bone tissue engineering
    Wang Xiao-feng, Wu Yan
    2013, 17 (19):  3558-3565.  doi: 10.3969/j.issn.2095-4344.2013.19.022
    Abstract ( 484 )   PDF (787KB) ( 652 )   Save

    BACKGROUND: Seed cells suitable for bone tissue engineering can be provided by culture of the stem cells known to have the potential of osteoblast differentiation or newly found.
    OBJECTIVE: To review the isolation and culture methods, biological characteristics and markers of diverse stem cells used for bone tissue engineering.
    METHODS: A computer-based online retrieval of PubMed and CNKI databases was performed to search papers published between 1995 and 2012 using the key words “bone tissue engineering, seed cells, stem cells, osteoblast differentiation” in English and Chinese. A total of 50 papers were suitable for final analysis from three aspects including isolation and culture methods, basic characteristics of stem cells and their application in bone tissue engineering.
    RESULTS AND CONCLUSION: The isolation and culture methods, biological characteristics and marker of diverse stem cells including embryonic stem cells, bone marrow mesenchymal stem cells, synovial membrane mesenchymal stem cells, umbilical cord mesenchymal stem cells, umbilical cord mesenchymal stem cells, peripheral blood-derived multi-potent mesenchymal stem cells, adipose-derived stem cells, endometrial stem cells and dental pulp stem cells. There have been four methods used to isolate and purify bone marrow mesenchymal stem cells including density gradient centrifugation, whole bone marrow adherence method, flow cytometry and immunomagnetic bead method. These findings indicate that diverse stem cells have the capacity to differentiate into osteoblasts under specific conditions.

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    Correlation of Alzheimer’s disease with Wnt signaling pathway and neural stem cells
    Wang Wei, Zhang Hai-ting, Wang Shu-hui, Zhang Yong-bo
    2013, 17 (19):  3566-3572.  doi: 10.3969/j.issn.2095-4344.2013.19.023
    Abstract ( 394 )   PDF (584KB) ( 915 )   Save

    BACKGROUND: The pathological mechanism of Alzheimer’s disease involves inherited, environmental and immunological factors. Strong evidence exists that Wnt signaling pathway is closely related to the pathological process of Alzheimer’s disease. There is also evidence that Wnt signaling pathway plays a crucial effect on the proliferation of neural stem cells.
    OBJECTIVE: To review the relationship between pathological process of Alzheimer’s disease and Wnt signaling pathway and effects of Wnt signaling on proliferation and differentiation of neural stem cells, providing theoretical evidence for treatment of Alzheimer’s disease.
    METHODS: A computer-based online search of PubMed databases was undertaken for papers addressing the relationship of Alzheimer’s disease and Wnt signaling pathway and the correlation between Wnt signaling pathway and neural stem cells using the key words “Alzheimer’s disease, Wnt signaling pathway, NSCs, stem cell differentiation, amyloid-β protein, protein Tau”. After excluding papers with repetitive contents, 50 papers were suitable for final analysis.
    RESULTS AND CONCLUSION: Treatment of neurodegenerative diseases characterized by neuron loss using neural stem cell transplantation has become a gradually increased research area. However, how to regulate neural stem cells to differentiate into specific neurons has been proposed. Signal transduction plays an important role in the differentiation of neural stem cells and Wnt signaling pathway is an important extracellular factor of regulating the proliferation and differentiation of neural stem cells. Inactivation of Wnt signaling pathway promotes the progression of Alzheimer’s disease, and activation of Wnt signaling pathway protects hippocampal neurons and promotes the differentiation of neural stem cells. This may provide novel therapeutic methods for Alzheimer’s disease.

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    Prospects and problems of stem cells in the treatment of neurodegenerative diseases
    Xiong Jie, Ning Li-na, Wang Zai-ling, Shi Xue-min
    2013, 17 (19):  3573-3580.  doi: 10.3969/j.issn.2095-4344.2013.19.024
    Abstract ( 721 )   PDF (693KB) ( 954 )   Save

    BACKGROUND: Although the incidence of neurodegenerative diseases in various populations is high and has an upward trend, so far there is no effective treatment method. So it is a challenge for scientific community to seek effective treatment method for the treatment of neurodegenerative diseases.
    OBJECTIVE: To analyze and review the research progress and hot issues of stem cells for the treatment of neurodegenerative diseases.
    METHODS: The basic and clinical researches on stem cells for the treatment of neurodegenerative diseases were overviewed, including Alzheimer’s disease, Parkinson’s disease, stroke, Huntington’s disease, retinitis pigmentosa, amyotrophic lateral sclerosis and epilepsy, in order to investigate the feasibility, advantages and problems of stem cells in the treatment of neurodegenerative diseases.
    RESULTS AND CONCLUSION: Most of the studies on stem cells in the treatment of neurodegenerative diseases are in the stage of experimental animal models, and there is no valid evidence to support stem cell therapy. There is no exact clinical assurance and standards on the safety and efficacy of stem cells for the treatment of neurodegenerative diseases, and the clinical efficacy and adverse reactions need to be further verified with large-sample long-term clinical trials.

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    Clinical progress in olfactory ensheathing cell transplantation for treatment of chronic spinal cord injury
    Wen Jian, Wang Yan-song, Wei Li, Li Jie
    2013, 17 (19):  3581-3588.  doi: 10.3969/j.issn.2095-4344.2013.19.025
    Abstract ( 345 )   PDF (831KB) ( 471 )   Save

    BACKGROUND: A large number of in vitro and animal experiments have demonstrated the effects of olfactory ensheathing cells in the repair of spinal cord injury, but the clinical studies regarding olfactory ensheathing cell transplantation for the treatment of spinal cord injury are in infancy.
    OBJECTIVE: To investigate the clinical safety, efficacy and practicality of the olfactory ensheathing cell transplantation for treatment of chronic spinal cord injury.
    METHODS: Using “olfactory ensheathing cells, spinal cord injury, clinical research” as keywords, the first author retrieved PubMed databases and CNKI database for papers regarding clinical studies on olfactory ensheathing cell transplantation for treatment of chronic spinal cord injury as well as clinical safety and effectiveness published before May 2012.
    RESULTS AND CONCLUSION: A total of 133 papers were initially retrieved. After reading titles and abstracts, repetitive studies were excluded and 34 papers were included in the final analysis. Olfactory ensheathing cell transplantation for spinal cord injury has acquired good efficacy in in vitro and animal experiments. In the clinical trials, there are several sources of olfactory ensheathing cells used in treatment of chronic spinal cord injury: (1) embryonic olfactory ensheathing cell transplantation; (2) olfactory mucosa transplantation; (3) olfactory mucosa-derived olfactory ensheathing cell transplantation. The oval safety and efficacy of three kinds of olfactory ensheathing cell transplantation methods are 96.4% and 23.4%, respectively, but there are obvious limitations. These findings suggest that the safety and efficacy of olfactory ensheathing cell transplantation in the treatment of chronic spinal cord injury need further investigation and there is a long road ahead for clinical application.

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    Research progress in autologous cardiac stem cell transplantation for treatment of ischemic cardiomyopathy
    Hou Hong, Lü An-lin, Hou Jing, Liu Bo-wu, Da Jing, Hou Zhao-lei, Yang Na
    2013, 17 (19):  3589-3595.  doi: 10.3969/j.issn.2095-4344.2013.19.026
    Abstract ( 296 )   PDF (593KB) ( 316 )   Save

    BACKGROUND: Drugs, interventional or surgical treatment cannot fundamentally solve the loss of myocardial cells after ischemic infarction. Many studies have shown that autologous cardiac stem cells transplantation for treatment of ischemic cardiomyopathy is safe and feasible, and it can produce the neonatal cardiac myocytes, reduce the size of infarct scar, inhibit the ventricular remodeling and improve cardiac function. At present, autologous cardiac stem cells transplantation for treatment of ischemic cardiomyopathy has entered clinical trials.
    OBJECTIVE: To summarize the research progress of autologous cardiac stem cells transplantation for treatment of ischemic cardiomyopathy at home and abroad in recent years.
    METHODS: The first author retrieved PubMed database and China Academic Journal article from January 1998 to April 2012 using computer. The key words were “autologous, cardiac stem cells, ischemic cardiomyopathy, transplantation, treatment”. We retrieved 82 articles, and 57 articles were included in the review.
    RESULTS AND CONCLUSION: Transplantation of cardiac stem cells derived from autologous heart tissue to the ischemic infarction region of the heart can differentiate and generate new cardiomyocytes as well as endothelial cells, inhibit ventricular remodeling, and improve cardiac regional systolic and diastolic function. Transplantation of autologous cardiac stem cells provides a new therapeutic approach for the treatment of ischemic cardiomyopathy. Compared to other sources of stem cells, transplantation of autologous cardiac stem cells for treatment of ischemic cardiomyopathy has higher clinical value.

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    Application of dental pulp stem cells in tissue engineering
    Shang Li-juan, Wu Yan
    2013, 17 (19):  3596-3602.  doi: 10.3969/j.issn.2095-4344.2013.19.027
    Abstract ( 311 )   PDF (657KB) ( 480 )   Save

    BACKGROUND: Dental pulp stem cells is a kind of adult stem cells derived from dental pulp and possess high proliferation rate, self-renewal capability and multi-differentiation capability. Dental pulp stem cells are possible cell sources for tissue engineering and are therefore used for prevention and treatment of tooth-related diseases in the clinic.
    OBJECTIVE: To summarize the current progress of dental pulp stem cells and their application in tissue engineering.
    METHODS: A computer-based online retrieval of CNKI and PubMed databases (2000-01/2012-05) was performed to search papers regarding dental pulp stem cells by inputting “dental pulp stem cells, culture, induced, differentiation” in the title and abstract search boxes. The papers published recently or in high impact journals were selected. A total of 205 papers were initially retrieved. Forty-four papers regarding sustained-release antimicrobials were suitable for final analysis.
    RESULTS AND CONCLUSION: Compared to other adult stem cells, there are many unsolved problems regarding dental pulp stem cells. With a gradual improvement in the scientific technology, these problems will be investigated and gradually solved. Dental pulp stem cells are promising seed cells for bone tissue engineering, dental tissue engineering and nerve tissue engineering. Dental pulp stem cells hold great promise in dental pulp regeneration and dental restoration.

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    Autoantibodies on bone marrow hematopoietic stem/progenitor cells and immunorelated pancytopenia
    Dong Ting, Li Zheng-fa, Ouyang Hong-mei, Shen Xiao-mei
    2013, 17 (19):  3603-3610.  doi: 10.3969/j.issn.2095-4344.2013.19.028
    Abstract ( 460 )   PDF (741KB) ( 460 )   Save

    BACKGROUND: mmunorelated pancytopenia involves in multiple clinical disciplines and has been paid more and more attention in recent years. Autoantibodies on bone marrow hematopoietic stem cells and immune regulation function may be the crux of the problem.
    OBJECTIVE: To study the progress on the role of bone marrow hematopoietic stem cell-associated antibodies in the pathogenesis of immunorelated pancytopenia.
    METHODS: A computer retrieval of PubMed, WangFang Med Online and CHKD database was conducted for articles regarding the autoantibodies on bone marrow hematopoietic stem cells published from March 1992 to March 2012. The keywords were “immunorelated pancytopenia, bone marrow hematopoietic cells, autoantibody, T helper 17 cells”. Repetitive articles were excluded, and finally 30 articles were included in result analysis.
    RESULTS AND CONCLUSION: The production of autoantibodies on bone marrow hematopoietic cells is due to the imbalance in T lymphocyte regulation resulting in abnormal quantity and function of B lymphocyte and its subset. They destroyed or inhibited the differentiation and maturation of bone marrow hematopoietic cells, leading to a reduction of peripheral blood cells eventually. The increasing number of T helper 17 cells and the hyperfunction of T helper 17 cells may be associated with the production of autoantibodies in patients with immunorelated pancytopenia, which is an important factor for the pathogenesis of immunorelated pancytopenia.

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