Human adipose tissue-derived stem cells differentiate into endothelial cells in vitro and improve postnatal neovascularization in vivo

被引:862
作者
Cao, Y
Sun, Z
Liao, LM
Meng, Y
Han, Q
Zhao, RCH [1 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Ctr Excellence Tissue Engn, Beijing 100730, Peoples R China
[2] Chinese Acad Med Sci, Sch Basic Med, Ctr Excellence Tissue Engn, Beijing 100730, Peoples R China
[3] Peking Union Med Coll, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
adipose; stein cells; endothelial; differentiation; inhibitor; ischemia;
D O I
10.1016/j.bbrc.2005.04.135
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this study, we isolated CD31(-), CD34(-), CD106(-) (VCAM-1(-)), and fetal liver kinase(+) (Flk1(+)) cells from adipose tissue. These cells can be induced to differentiate into cells of osteogenic and adipogenic lineages in vitro and were termed adipose derived adult stem cells (ADAS cells). We also showed that they have characteristics of endothelial progenitor cells. In vitro, ADAS cells expressed endothelial markers when cultured with VEGF. In vivo, ADAS cells can differentiate in response to local cues into endothelial cells that contributed to neoangiogenesis in hindlimb ischemia models. PI3 kinase inhibitor LY294002 blocked the differentiation of ADAS cells into endothelial cells in vitro. Because ADAS cells can be expanded in culture without obvious senescence for more than 20 population doublings, they may be a potential source of endothelial cells for cellular pro-angiogenic therapies. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:370 / 379
页数:10
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