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AGM区来源的基质细胞促进造血干细胞扩增的体外实验研究
引用本文:付劲蓉,刘文励,周玉峰,陈惠芹,周敦华,黄绍良.AGM区来源的基质细胞促进造血干细胞扩增的体外实验研究[J].中国病理生理杂志,2007,23(7):1373-1377.
作者姓名:付劲蓉  刘文励  周玉峰  陈惠芹  周敦华  黄绍良
作者单位:1 华中科技大学同济医学院附属同济医院血液科, 湖北 武汉 430030); 2
中山大学附属第二医院干细胞中心, 广东 广州 510120
摘    要:目的: 探讨主动脉-性腺-中肾(aorta-gonad-mesonephros,AGM)来源的基质细胞对造血干细胞(HSC)增殖的促进作用,为探寻HSC的体外扩增方法奠定实验基础。 方法: 分别从孕11 d BALB/c小鼠胚胎AGM区及6周龄小鼠骨髓分离、培养基质细胞,流式细胞仪等对基质细胞进行鉴定;利用小鼠胚胎干细胞(ESC)向造血细胞定向分化的模型,结合高增殖潜能集落(HPP-CFC)、原始细胞集落(BL-CFC)形成实验及流式细胞仪分析CD34+、CD34+Sca-1+细胞比例,对比研究AGM及骨髓基质细胞对ESC来源的HSC的扩增作用。 结果: 小鼠AGM和骨髓基质细胞在形态及表型上基本相似,均符合基质细胞的特征。AGM和骨髓基质细胞均可促进ESC来源的HPP-CFC的形成,但AGM基质细胞还可促进ESC来源的 BL-CFC的形成;流式细胞仪检测发现:在骨髓基质细胞支持下,CD34+细胞增加了3-4倍,但CD34+/Sca-1+却无明显增加;而在AGM基质细胞支持下CD34+、CD34+Sca-1+细胞均明显增加了4-5倍。 结论: AGM基质细胞在有效扩增小鼠HSC同时,能很好地维持HSC自我更新及多向分化的潜能。

关 键 词:主动脉-性腺-中肾  造血干细胞  
文章编号:1000-4718(2007)07-1373-05
收稿时间:2005-5-13
修稿时间:2005-05-132006-08-02

Supportive and expansive effects of aorta-gonad-mesonephros (AGM)-derived stromal cells on hematopoietic stem in vitro
FU Jin-rong,LIU Wen-li,ZHOU Yu-feng,CHEN Hui-qin,ZHOU Dun-hua,HUANG Shao-liang.Supportive and expansive effects of aorta-gonad-mesonephros (AGM)-derived stromal cells on hematopoietic stem in vitro[J].Chinese Journal of Pathophysiology,2007,23(7):1373-1377.
Authors:FU Jin-rong  LIU Wen-li  ZHOU Yu-feng  CHEN Hui-qin  ZHOU Dun-hua  HUANG Shao-liang
Institution:1 Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China; 2 Stem Cell Research Center, The Second Affiliated Hospital, Sun Yet-sen University, Guangzhou 510120, China. E-mail: jrfu@tjh.tjmu.edu.cn
Abstract:AIM:To explore the supportive and expansive effects of aorta-gonad-mesonephros(AGM) region derived stromal cells on hematopoietic stem cells(HSC) in vitro.METHODS:The murine stromal cells were separated and cultured from AGM region of a 11 day postcoitum(dpc) mouse embryo and 6 week mouse.After identification by Wright's staining and flow cytometry,the stromal cells were co-cultured with the embryonic stem cell(ESC)-derived,cytokine-induced HSCs,and the maintenance and expansion of HSCs were evaluated by detecting CD34 ,CD34 Sca-1 cells with flow cytometry.Blast colony-forming cell(BL-CFC) and high proliferative potential colony-forming cells(HPP-CFC) were determined by semi-solid medium clonal culture.RESULTS:AGM-derived and bone marrow(BM)-derived stromal cells were similar in morphology and phenotype,and had common character of stromal cells.Supported by AGM stromal cells or by BM stromal cells,more primitive progenitor cells HPP-CFC were expanded,but BL-CFC expansion was only detected in AGM-derived stromal cells.In the supporting of BM stromal cells CD34 hematopoietic stem/progenitor cells were expanded 3-4 times,but no significant expansion in CD34 Sca-1 cells was observed.While in the supporting of AGM stromal cells,both CD34 hematopoietic stem/progenitor cells and CD34 Sca-1 cells were expanded significantly from 4 to 5 times,respectively(P<0.05).CONCLUSION:AGM-derived stromal cells significantly support the expansion of HSC,and also maintain the self-renewal activity and multi-lineage differentiation of HSC in vitro.
Keywords:Aorta-gonad-mesonephros  Hematopoietic stem cells  Stromal cells
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