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内皮祖细胞体外扩增的特性

Characteristics of ex vivo expansion of endothelial progenitor cells.

作者信息

Liu Chao, Sun Zongquan, Wu Yongchao, Chen Xinzhong, Feng Jian'e

机构信息

Department of Cardiac Surgery, The Affiliated First Hospital of Zhengzhou University, Zhengzhou 450052, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2006;26(4):411-3. doi: 10.1007/s11596-006-0408-8.

Abstract

The characteristics for the ex vivo expansion of the endothelial progenitor cells (EPCs) were explored. CD34+ cells were selected from umbilical cord blood mononuclear cells (MNC) by MiniMACS system, expanded under the same conditions as those for total MNC, coincubation of CD34+ and CD34- from the same donor for EPCs. In addition, the effects of vessel endothelial growth factor (VEGF) and passage on cell differentiation, expansion kinetics and apoptosis were examined. EPCs were determined and quantified by immunocytochemistry and flow cytometry. The results showed that both coculture of CD34+ and CD34- and total MNC led to a significant increase in the expansion of CD34+ cells as compared with CD34 enrichment (P < 0.05). There was a tendency toward decreased apoptosis in cultures when early passage was performed immediately after cord like structures appeared. VEGF had no significant effect on apoptosis (P > 0.05). These differentiated EPCs were positive for CD34+, von Willebrand factor (vWF), KDR, CD31 staining and phagocytized acetylated low-density lipoprotein (LDL). CD34+ cells accounted for (68.2 +/- 6.3)% of attaching (AT) cells at day 7 of culture. It was suggested the most efficient method to ex vivo expansion of EPCs was coculture of CD34+ and CD34- or total MNC. Early passage makes cell apoptosis rate decrease. VEGF had no significant effect on ex vivo expansion of EPCs.

摘要

探讨了内皮祖细胞(EPCs)体外扩增的特性。通过MiniMACS系统从脐带血单个核细胞(MNC)中筛选出CD34+细胞,在与总MNC相同的条件下进行扩增,将来自同一供体的CD34+和CD34-细胞共同培养以获得EPCs。此外,还检测了血管内皮生长因子(VEGF)和传代对细胞分化、扩增动力学及凋亡的影响。通过免疫细胞化学和流式细胞术对EPCs进行鉴定和定量。结果显示,与CD34富集相比,CD34+和CD34-细胞共培养以及总MNC培养均导致CD34+细胞的扩增显著增加(P<0.05)。当在出现条索状结构后立即进行早期传代时,培养物中的凋亡有减少趋势。VEGF对凋亡无显著影响(P>0.05)。这些分化的EPCs对CD34+、血管性血友病因子(vWF)、激酶插入区受体(KDR)、CD31染色呈阳性,并吞噬乙酰化低密度脂蛋白(LDL)。在培养第7天时,CD34+细胞占贴壁(AT)细胞的(68.2±6.3)%。提示EPCs体外扩增的最有效方法是CD34+和CD34-细胞共培养或总MNC培养。早期传代可使细胞凋亡率降低。VEGF对EPCs的体外扩增无显著影响。

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