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人AGM区基质细胞对脐血LTC-IC的支持作用
引用本文:陈惠芹,张绪超,黄绍良,吴北燕,吴燕峰,包蓉. 人AGM区基质细胞对脐血LTC-IC的支持作用[J]. 中国实验血液学杂志, 2006, 14(1): 94-97
作者姓名:陈惠芹  张绪超  黄绍良  吴北燕  吴燕峰  包蓉
作者单位:中山大学附属第二医院干细胞研究中心,广州,510120
基金项目:中国科学院资助项目;高等学校博士学科点专项科研项目;国家科技攻关项目
摘    要:为探讨人主动脉-性腺-中肾(AGM)区基质细胞对脐血长期培养启动细胞(LTC-IC)的造血支持作用,建立了人AGM区基质细胞与脐血CD34+细胞体外长期共培养体系。采用免疫磁珠方法分离人脐血CD34+细胞,接种于已制备好人AGM区基质细胞(hAGMS1-S5)饲养层的24孔板中共培养,同时设无饲养层组作为对照,分别于共培养5、6、7、8周时收获细胞行造血细胞集落培养,并采用极限稀释法(LDA)检测与人AGM区基质细胞共培养后的脐血CD34+细胞的LTC-IC含量。结果表明,无饲养层的对照组培养5周后不再产生造血细胞集落,而以hAGMS1-S5作为饲养层,共培养5周后造血细胞仍具有集落形成能力。hAGMS1-S5维持LTC-IC的作用组间比较有显著性差异(P<0.05),其中以hAGMS3与S4组支持作用最强。LDA检测结果显示,hAGMS3和S4维持LTC-IC的能力无显著性差异(P>0.05);与hAGMS3和S4共培养14天后脐血CD34+细胞中的LTC-IC扩增,分别是达到(176±46)%、(187±52)%,S3和S4两组间比较无显著性差异(P>0.05)。结论:人AGM区基质细胞S1-S5对脐血LTC-IC具有维持作用,特别是hAGMS3和S4两株细胞对脐血LTC-IC具有更好的维持及扩增作用。

关 键 词:AGM区  基质细胞  长期培养启动细胞  脐血
文章编号:1009-2137(2006)01-0094-04
收稿时间:2005-06-20
修稿时间:2005-07-17

Supportive Effects of Human Aorta-Gonad-Mesonephros-Derived Stromal Cells on Umbilical Cord blood LTC-IC
CHEN Hui-Qin,ZHANG Xu-Chao,HUANG Shao-Liang,WU Bei-Yan,WU Yan-Feng,BAO Rong. Supportive Effects of Human Aorta-Gonad-Mesonephros-Derived Stromal Cells on Umbilical Cord blood LTC-IC[J]. Journal of experimental hematology, 2006, 14(1): 94-97
Authors:CHEN Hui-Qin  ZHANG Xu-Chao  HUANG Shao-Liang  WU Bei-Yan  WU Yan-Feng  BAO Rong
Affiliation:Center for Stem Cell Research, The Second Affiliated Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Abstract:The objective of this study was to explore the supportive effects of human aorta-gonad-mesonephros (AGM)-derived stromal cells on human umbilical cord blood long-term culture-initiating cells (LTC-IC). A co-culture system was established with human AGM stromal cells and umbilical cord blood CD34(+) cells. Different stromal cells derived from human AGM region (hAGM S1-S5) were plated on 24-well plates as feeder cells. CD34(+) cells were positively selected from human umbilical cord blood through immunomagnetic bead selection method, seeded on the feeder cells, and co-cultured for 8 weeks. The hematopoietic cells were collected at 5, 6, 7 and 8 weeks for CFC analysis. Frequencies of LTC-IC in umbilical cord blood CD34(+) cells after co-culture with AGM stromal cells were detected through limiting dilute analysis (LDA). The results showed that there was no any hematopoietic CFC in the feeder cell-free culture system after 5 weeks of co-culture. However, in AGM feeder cells culture systems, there were still CFCs after 5 weeks of co-culture, which indicated that human AGM stromal cells could maintain LTC-IC in vitro. In groups of hAGM feeders, hAGMS3 and S4 had better supportive effects than other AGM groups (P < 0.05). The absolute number of LTC-IC in hAGM S3 and S4 culture systems got expansion up to (176 +/- 46)% and (187 +/- 52)% respectively without significant difference between hAGMS3 and S4 (P > 0.05). It is concluded that human AGM stromal cells S1-S5 support the maintenance of umbilical blood LTC-IC in vitro, while hAGMS3 and S4 cells have better effects on maintaining LTC-IC and expansion of LTC-IC.
Keywords:AGM region    stromal cell    LTC-IC   cord blood
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