Fibroblast growth factor-transforming growth factor beta dialogues, endothelial cell to mesenchymal transition, and atherosclerosis

被引:20
|
作者
Chen, Pei-Yu [1 ]
Simons, Michael [1 ,2 ]
机构
[1] Yale Cardiovasc Res Ctr, Dept Internal Med, New Haven, CT USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
关键词
atherosclerosis; endothelial-to-mesenchymal transition; fibroblast growth factor; transforming growth factor beta; SMOOTH-MUSCLE ACTIN; TGF-BETA; GENE-EXPRESSION; B-CELLS; MECHANISMS; PATHOPHYSIOLOGY; CONTRIBUTES; DYSFUNCTION; DISRUPTION; RESPONSES;
D O I
10.1097/MOL.0000000000000542
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Purpose of review Despite much effort, atherosclerosis remains an important public health problem, leading to substantial morbidity and mortality worldwide. The purpose of this review is to provide an understanding of the role of endothelial cell fate change in atherosclerosis process. Recent findings Recent studies indicate that a process known as endothelial-to-mesenchymal transition (EndMT) may play an important role in atherosclerosis development. Transforming growth factor beta (TGFb) has been shown to be an important driver of the endothelial cell phenotype transition. Summary The current review deals with the current state of knowledge regarding EndMT's role in atherosclerosis and its regulation by fibroblast growth factor (FGF)-TGFb cross-talk. A better understanding of FGF-TGFb signaling in the regulation of endothelial cell phenotypes is key to the development of novel therapeutic agents.
引用
收藏
页码:397 / 403
页数:7
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