王冬月, 王昭领, 朱国雄, 吴高义, 周楠, 张飞龙, 陈海英. 碱性成纤维细胞生长因子对类雪旺细胞形成及增殖的影响[J]. 解放军医学院学报, 2016, 37(6): 630-633. DOI: 10.3969/j.issn.2095-5227.2016.06.027
引用本文: 王冬月, 王昭领, 朱国雄, 吴高义, 周楠, 张飞龙, 陈海英. 碱性成纤维细胞生长因子对类雪旺细胞形成及增殖的影响[J]. 解放军医学院学报, 2016, 37(6): 630-633. DOI: 10.3969/j.issn.2095-5227.2016.06.027
WANG Dongyue, WANG Zhaoling, ZHU Guoxiong, WU Gaoyi, ZHOU Nan, ZHANG Feilong, CHEN Haiying. Effect of basic fibroblast growth factor on formation and proliferation of Schwann-like cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(6): 630-633. DOI: 10.3969/j.issn.2095-5227.2016.06.027
Citation: WANG Dongyue, WANG Zhaoling, ZHU Guoxiong, WU Gaoyi, ZHOU Nan, ZHANG Feilong, CHEN Haiying. Effect of basic fibroblast growth factor on formation and proliferation of Schwann-like cells[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2016, 37(6): 630-633. DOI: 10.3969/j.issn.2095-5227.2016.06.027

碱性成纤维细胞生长因子对类雪旺细胞形成及增殖的影响

Effect of basic fibroblast growth factor on formation and proliferation of Schwann-like cells

  • 摘要: 目的 探讨碱性成纤维细胞生长因子(basic fibroblast growth factor,b-FGF)在人脐带间充质干细胞(human umbilical cord mesenchymal stem cells,hUCMSCs)向类雪旺细胞诱导过程中的作用及其对类雪旺细胞增殖的影响。 方法 培养鉴定hUCMSCs,经预诱导后将细胞分组,继续培养7 d。A1组为普通培养基组,B1组为普通培养基+ b-FGF组,C1组为普通培养基+经典诱导成分组,D1组为C1组基础上剔除b-FGF,通过形态学及S100免疫荧光对类雪旺细胞进行鉴定,并记录各组类雪旺细胞数目及S100阳性率,分析b-FGF在诱导过程中的作用。将诱导的类雪旺细胞经纯化后分组培养2 d、4 d、6 d:A2组为普通培养基组,B2组为普通培养基+ b-FGF组,检测b-FGF对类雪旺细胞增殖的影响。 结果 在诱导实验中,A1组未见明显类雪旺细胞,S100染色阴性,B1、C1、D1组均可见类雪旺细胞形态,S100染色阳性。类雪旺细胞数目及S100阳性率:A1组< B1组< C1组(P< 0.05),D1组< C1组(P< 0.05)。在促增殖实验中,各时间点OD值:B2组> A2组(P< 0.05)。 结论 b-FGF可促进hUCMSCs向类雪旺细胞转化,并可促进诱导后类雪旺细胞的增殖。

     

    Abstract: Objective To investigate the function of basic fibroblast growth factor (b-FGF) in the process of human umbilical cord mesenchymal stem cells (HUCMSCs) differentiating to Schwann-like cells, and its effect on proliferation of Schwann-like cells. Methods HUCMSCs were cultured and identified.After pre-induction, the cells were randomly divided into four groups and cultured continuously for 7 days (normal medium as group A1, normal medium with bFGF as group B1, normal medium with the classic cytokine cocktail as group C1 and C1 minus b-FGF as group D1).Schwann-like cells were identified by morphology and S100 immunofluorescence.Then the number of Schwann-like cells in each group was counted and the positive rate of S100 was calculated to analyze the role of b-FGF in the induction process; The Schwann-like cells were divided into two groups (normal medium as group A2, normal medium with bFGF as group B2) and cultured to observe the influence of b-FGF on proliferation of Schwann-like cells at day 2, 4, 6. Results In the experiments of induction, Schwann-like cells were not obvious in group A1 with S100 showing negative, and the cells were found in group B1, C1 and D1 with S100 showing positive.The number of Schwann-like cells and expression of S100 in each group were A1< B1< C1 (P< 0.05), D1< C1 (P< 0.05).In the experiments of proliferation, OD value at different time points in two groups were B2> A2 (P< 0.05). Conclusion b-FGF can not only promote hUCMSCs transform into Schwann-like cells, but also be in favor of the proliferation of Schwann-like cells.

     

/

返回文章
返回