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作 者:王东[1] 刘来有[1] 武展雄[1] 孙海钰[1] 刘越连[1]
机构地区:[1]山西医科大学第二临床医学院骨科,太原030001
出 处:《山西医科大学学报》2006年第5期484-488,共5页Journal of Shanxi Medical University
基 金:山西省归国留学人员科研基金资助项目(200262)
摘 要:目的体外培养骨髓间质细胞,探索大鼠骨髓间质细胞体外诱导及向神经细胞方向分化。方法分离大鼠骨髓间质细胞培养、扩增,检查细胞活力。应用脑神经营养因子(BDNF)、β-巯基乙醇(-βME)对细胞诱导分化,行大体观察,6 h后免疫组织化鉴定神经丝蛋白(NF-200)、神经烯醇化酶(NSE)、胶质纤维酸性蛋白(GFAP),并用RT-PCR鉴定NF-200、NSE和GFAP的mRNA表达情况。结果用BDNF、-βME单独或者共同诱导3 h,骨髓间质细胞形态类似神经细胞,6 h后神经细胞标记蛋白和mRNA表达阳性,而且BDNF+-βME组诱导率最高。结论BDNF和-βME能协同刺激大鼠骨髓间质细胞转化并分化为神经细胞。Objective To observe the growth and differentiation of cultured rat bone marrow cells (MSCs) to neural cells. Methods Purified MSCs were induced by β-mercaptoethanol(β-ME)alone or combination of brain derived neurotrophic factor(BDNF) with β-ME. After 6 h incubation, neuron special endolase (NSE), neurofilament (NF-200) and glial fibrillary acidic protein (GFAP) were detected by immunohistochemostry,and mRNAs of NSE, NF-200 and GFAP were detected with reverse transcriptase-polymerase chain reaction (RT-PCR) and the cells with vitality were observed. Results After induction with β-ME or BDNF alone or together, some MSCs exhibited the phenotypes of neural cells. After 6 h induction, NSE and NF-200 positive cells increased significantly. It was the same in the mRNA. Furthermore, the addition of BDNF and β-ME caused the maximal variation. Conclusion Combination of β-ME with BDNF may synergistically promote the transformation of MSCs and differentiation into neurons.
分 类 号:R329[医药卫生—人体解剖和组织胚胎学]
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