Chen Hui-qin, Zhang Xu-chao, Huang Shao-Liang, Wu Bei-yan, Wu Yan-feng, Cai Yun
Stem Cell Research Center, The Second Affiliated Hospital, Sun Yat-sen University, Guangzhou 510120, China.
Zhonghua Xue Ye Xue Za Zhi. 2006 Jun;27(6):390-3.
To explore the supportive effects of stromal cells from human aorta-gonad-mesonephros (AGM) region on umbilical cord blood CD34+ cells.
Stromal cells derived from human AGM region (hAGMS1-S5) and fetal trunk fibroblasts (hFf) were cultured on the bottom of 24-well plates as feeder cells. CD34+ cells positively selected from human umbilical cord blood through immunomagnetic beads selection method, were seeded into 24-well plates, and co-cultured for 28d. The number of total nucleated cells (TNC), CD34+ cells, CD34+ CD38- cells, and CFC were counted every week.
Stromal cells from human AGM region significantly supported proliferation of the TNC, CD34+ cells, CD34+ CD38- cells and CFC, when compared with hFT and controls without feeder cells (P < 0.05). The TNC increased (25.13 +/- 4.83)-fold (peak value) at day 21 in group of co-culture with AGM stromal cells. CD34 and CD34+ CD38- cells increased (2.68 +/- 0.51)- and (2. 38 +/- 0.45)-fold respectively at day 14 of co-culture. In colony analysis, HPP-CFU increased (2.62 +/- 0.85)-fold at day 14 of co-culture. The supportive effects of human AGM S1-S5 were significantly different, hAGM S3 and S4 were better than hAGM SI, S2, and S5 (P < 0.05).
Human AGM stromal cells S1-S5 could support the maintenance and expansion of umbilical cord blood CD34+ cells in vitro. hAGMS3, S4 cell had better effects on maintaining HSC activity, which would provide model cells and basic data for researches on hematopoiesis mechanism and hematopoietic differentiation of embryonic stem cells.
探讨人主动脉-性腺-中肾(AGM)区基质细胞对脐血CD34+细胞的支持作用。
将人AGM区来源的基质细胞(hAGMS1-S5)和胎儿躯干成纤维细胞(hFf)作为饲养细胞培养于24孔板底部。通过免疫磁珠筛选法从人脐血中阳性选择CD34+细胞,接种于24孔板中,共培养28天。每周计数总核细胞(TNC)、CD34+细胞、CD34+CD38-细胞和集落形成细胞(CFC)的数量。
与人胎儿躯干成纤维细胞及无饲养细胞的对照组相比,人AGM区基质细胞能显著支持TNC、CD34+细胞、CD34+CD38-细胞和CFC的增殖(P<0.05)。与AGM基质细胞共培养组在第21天时TNC增加了(25.13±4.83)倍(峰值)。共培养第14天时,CD34和CD34+CD38-细胞分别增加了(2.68±0.51)倍和(2.38±0.45)倍。在集落分析中,共培养第14天时高增殖潜能集落形成单位(HPP-CFU)增加了(2.62±0.85)倍。人AGM S1-S5的支持作用有显著差异,hAGM S3和S4优于hAGM S1、S2和S5(P<0.05)。
人AGM基质细胞S1-S5能在体外支持脐血CD34+细胞维持和扩增。hAGM S3、S4细胞对维持造血干细胞活性效果更好,可为胚胎干细胞造血机制及造血分化研究提供模型细胞和基础数据。