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人胚胎脐血间质干细胞生物学特性研究
引用本文:朱美玲,那晓东,雷俊霞,刘华,胡燕芬,黄玲惠,黄伟花,张秀明,李树浓. 人胚胎脐血间质干细胞生物学特性研究[J]. 中国病理生理杂志, 2004, 20(6): 1003-1008
作者姓名:朱美玲  那晓东  雷俊霞  刘华  胡燕芬  黄玲惠  黄伟花  张秀明  李树浓
作者单位:1. 中山大学中山医学院病理生理学教研室, 广东 广州 510089;
2. 深圳市宝安区血站脐血库, 广东 深圳 518101;
3. 深圳市宝安区西乡人民医院, 广东 深圳 518102
基金项目:国家重点基础研究项目 (No .2 0 0 1CB5 0 990 4 ),广东省十五重大攻关项目资助 (2 0 0 1A30 2 0 10 1)
摘    要:目的:研究人中期胚胎脐血间质干细胞生物学特性,探讨其在自体宫内基因转移/治疗(IUGT)领域的应用前景。方法: 采用L-DMEM完全培养液培养中期胚胎脐血间质干细胞(MSC);流式细胞仪技术检测细胞表面标记;地塞米松/胰岛素等作为脂肪细胞诱导液,β-甘油磷酸钠/抗坏血酸等作为成骨细胞诱导液分别诱导细胞分化;将携带有绿色荧光蛋白的重组腺病毒转染MSC,荧光显微镜下检测MSC表达转基因特性;F344新生大鼠肝内注射MSC,免疫荧光检测6周后不同组织器官中人MSC存在;非肥胖型糖尿病/重症联合免疫缺陷性小鼠(NOD/SCID)皮下注射MSC,病理切片检测第30 d细胞体内成瘤性。 结果:3 mL人中期胚胎脐血可以分离、培养出MSC,细胞均一地表达CD29、CD44、CD59、CD105、CD166,不表达CD34、CD45、CD80、CD86、CD42a、HLA-DR分子,体外培养中具有成脂、成骨能力;细胞表达转基因产物绿色荧光蛋白阳性率高达56.32%±3.28%;在新生大鼠体内,人中期胚胎脐血来源的MSC能向多个不同组织器官迁移,在NOD/SCID小鼠内不具有成瘤性。结论:人中期胚胎脐血MSC适合中、晚期胚胎自体IUGT靶细胞。

关 键 词:胎血  间质干细胞  基因疗法  基因转移  水平  
文章编号:1000-4718(2004)06-1003-06
收稿时间:2003-09-23
修稿时间:2003-12-23

Biological characterics of human fetal cord blood mesenchymal stem cells
ZHU Mei-ling,NA Xiao-dong,LEI Jun-xia,LIU Hua,HU Yan-fen,HUANG Ling-hui,HUANG Wei-hua,ZHANG Xiu-ming,LI Shu-nong. Biological characterics of human fetal cord blood mesenchymal stem cells[J]. Chinese Journal of Pathophysiology, 2004, 20(6): 1003-1008
Authors:ZHU Mei-ling  NA Xiao-dong  LEI Jun-xia  LIU Hua  HU Yan-fen  HUANG Ling-hui  HUANG Wei-hua  ZHANG Xiu-ming  LI Shu-nong
Affiliation:1. Department of Pathophysiology, Sun Yat-sen Medical College, Zhongshan University, Guangzhou 510089, China;
2. Shenzhen Baoan Blood Center and Cord Blood Bank, Shenzhen 518101, China;
3. Shenzhen Baoan Xixiang Hospital, Shenzhen 518101, China
Abstract:AIM: To investigate the biological characterics of human second-trimester fetal cord blood mesenchymal stem cells (MSC) and its application prospects in utero gene transfer/therapy (IUGT). METHODS: Nuclear cells separated from cord blood were cultured in DMEM medium. Surface antigens of the MSC were analyzed by the FACScan flow cytometry. Adipogenic and osteogenic mediums were used to assess the differentiation ability of the cells. Adenovirus vector deliver green fluorescent protein gene (Ad-GFP) was used to transfected the MSC and the expressing of GFP was detected by fluorescent microscope. The MSC were injected into the liver of newborn rat. The immunofluorescence analysis was conducted to determine the presence of double-positive CD105+/CD166+ cells in different organs of rats. MSC were subcutaneous injected into the human-nonobese diabetes/severe combined immunodeficiency disease (NOD/SCID) mice and carcinogenesises of the MSC in vivo were detected by pathological diagnosis. RESULTS: MSC could be separated from fetal cord blood. These cells were uniformly positive for CD29, CD44, CD59, CD105, CD166 and negative for CD34, CD45, CD80, CD86, HLA-DR. The cells had the abilities to differentiate into adipogenic and osteogenic cells in vitro, expressed the GFP at high levels (56.32%±3.28%). The MSC were located at different organs after injected into the newborn rats and didn't have carcinogenicity in vivo. CONCLUSION: Human second-trimester fetal cord blood MSC is an promising target cells in fetal IUGT.
Keywords:Fetal blood  Mesenchymal stem cells  Gene therapy  Gene transfer   horizontal
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