A Role for Partial Endothelial-Mesenchymal Transitions in Angiogenesis?

被引:154
|
作者
Welch-Reardon, Katrina M. [1 ]
Wu, Nan [1 ]
Hughes, Christopher C. W. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Dept Mol Biol & Biochem, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biomed Engn, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Edwards Lifesci Ctr Adv Cardiovasc Technol, Irvine, CA 92697 USA
基金
美国国家卫生研究院;
关键词
angiogenesis; EMT; endothelial; transcription factor; GROWTH-FACTOR-BETA; TGF-BETA; CARDIAC FIBROSIS; VALVE DEVELOPMENT; KIDNEY FIBROSIS; BHLH FACTORS; E-CADHERIN; IN-VITRO; NOTCH; CELLS;
D O I
10.1161/ATVBAHA.114.303220
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The contribution of epithelial-to-mesenchymal transitions (EMT) in both developmental and pathological conditions has been widely recognized and studied. In a parallel process, governed by a similar set of signaling and transcription factors, endothelial-to-mesenchymal transitions (EndoMT) contribute to heart valve formation and the generation of cancer-associated fibroblasts. During angiogenic sprouting, endothelial cells express many of the same genes and break down basement membrane; however, they retain intercellular junctions and migrate as a connected train of cells rather than as individual cells. This has been termed a partial endothelial-to-mesenchymal transition. A key regulatory check-point determines whether cells undergo a full or a partial epithelial-to-mesenchymal transitions/endothelial-to-mesenchymal transition; however, very little is known about how this switch is controlled. Here we discuss these developmental/pathological pathways, with a particular focus on their role in vascular biology.
引用
收藏
页码:303 / 308
页数:6
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