首页 | 本学科首页   官方微博 | 高级检索  
检索        

诱导成鼠骨髓源神经干细胞的实验研究
引用本文:杜劲松,王剑,张信英.诱导成鼠骨髓源神经干细胞的实验研究[J].中国脊柱脊髓杂志,2004,14(8):483-485,i001.
作者姓名:杜劲松  王剑  张信英
作者单位:哈尔滨医科大学附属第一医院骨科,150001,黑龙江省哈尔滨市
摘    要:目的:探讨体外诱导成鼠骨髓源神经干细胞的可行性。方法:以含20ng/ml碱性成纤维生长因子(basic fibroblast growth factor,bFGF)与表皮生长因子(epidermal growth factor,EGF)的无血清培养液培养成鼠骨髓细胞,待细胞球形成后进行传代培养与单细胞克隆试验.以含100ng/ml bFGF培养液诱导分化,细胞免疫组化染色进行细胞鉴定。结果:骨髓细胞在诱导条件下形成表达Nestin抗原的细胞球.亦表达造血干细胞标志性抗原CD90。分离成单细胞后很快形成新的细胞球,并可分化出神经元与胶质细胞。结论:骨髓细胞可在体外诱导为能自我增殖的神经干细胞。

关 键 词:诱导    骨髓源  神经干细胞  实验研究
文章编号:1004-406X(2004)-08-0483-03

Study of induction of neural stem cells derived from adult rat bone marrow
DU Jinsong,WANG Jian,ZHANG Xinying.Study of induction of neural stem cells derived from adult rat bone marrow[J].Chinese Journal of Spine and Spinal Cord,2004,14(8):483-485,i001.
Authors:DU Jinsong  WANG Jian  ZHANG Xinying
Institution:DU Jinsong,WANG Jian,ZHANG Xinying Department of Orthopeadics,the First Hospital Affiliated to the Harbin Medical University,Harbin,150001,China
Abstract:Objective:To investigate induction of neural stem cells from adult rat bone marrow in vitro.Method:Bone marrow cells were cultivated in serum-free medium with 20ng/ml basic fibroblast growth factor(bFGF) and epidermal growth factor(EGF).After cellular spheres forming,primary spheres were mechanically dissociated and were cultivated or performed single-cell cloning test.Spheres were differentiated in medium with 100ng/ml bFGF,then immunocytochemistry test were performed.Result:In inductive situation,bone marrow could give rise to cellular spheres.The spheres expressed nestin,a neural stem cell marker,as well as CD90,a marker of hematopoietic stem cells.New spheres could soon form after being dissociated,and spheres could differationate into neurons and glial cells.Conclusion:Bone marrow cells can be induced to neural stem cells with self-proliferation characteristics.
Keywords:Bone marrow  Neural stem cell  Differentiation  
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国脊柱脊髓杂志》浏览原始摘要信息
点击此处可从《中国脊柱脊髓杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号