Endothelial origin of mesenchymal stem cells

被引:42
|
作者
Slukvin, Igor I. [1 ,2 ]
Vodyanik, Maxim [2 ]
机构
[1] Univ Wisconsin, Dept Pathol & Lab Med, Sch Med & Publ Hlth, Madison, WI 53706 USA
[2] Univ Wisconsin, Grad Sch, Natl Primate Res Ctr, Madison, WI 53706 USA
关键词
mesenchymoangioblast; hemangioblast; human embryonic stem cells; endothelial-mesenchymal transition; epithelial-mesenchymal transition; mesenchymal stem cells; endothelial cells; apelin receptor; FGF; AORTIC ENDOTHELIUM; STROMAL CELLS; QUAIL EMBRYO; IN-VIVO; TRANSITION; DIFFERENTIATION; VASCULOGENESIS; TISSUES; BONE; HEMATOPOIESIS;
D O I
10.4161/cc.10.9.15345
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mesenchymal stem/stromal cells (MSCs) are fibroblastoid cells capable of long-term expansion and skeletogenic differentiation. While MSCs are known to originate from neural crest and mesoderm, immediate mesodermal precursors that give rise to MSCs have not been characterized. Recently, using human embryonic stem cells (hESCs), we demonstrated that mesodermal MSCs arise from APLNR(+) precursors with angiogenic potential, mesenchymoangioblasts, which can be identified by FGF2-dependent colony-forming assay in serum-free semisolid medium. In this overview we provide additional insights on cellular pathways leading to MSC establishment from mesoderm, with special emphasis on endothelial-mesenchymal transition as a critical step in MSC formation. In addition, we highlight an essential role of FGF2 in induction of angiogenic cells with potential to transform into MSCs (mesenchymoangioblasts) or hematopoietic cells (hemangioblasts) from mesoderm, and discuss correlations of our in vitro findings with the course of angioblast development during embryogenesis.
引用
收藏
页码:1370 / 1373
页数:4
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