TGF-β-Induced Endothelial to Mesenchymal Transition in Disease and Tissue Engineering

被引：180

作者：

Ma, Jin ^{[1
,2
]}

Sanchez-Duffhues, Gonzalo ^{[1
]}

Goumans, Marie-Jose ^{[1
]}

ten Dijke, Peter ^{[1
,2
]}

机构：

[1] Leiden Univ, Med Ctr, Dept Cell & Chem Biol, Leiden, Netherlands

[2] Leiden Univ, Med Ctr, Oncode Inst, Leiden, Netherlands

来源：

FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | 2020年 / 8卷

关键词：

cancer-associated fibroblast; cardiovascular disease; EndMT; fibrosis; signal transduction; Smad; TGF-beta; tissue regeneration; GROWTH-FACTOR-BETA; PULMONARY ARTERIAL-HYPERTENSION; II RECEPTOR; SIGNALING PATHWAYS; CELLS; ENDMT; FIBROBLASTS; EXPRESSION; FIBROSIS; FAMILY;

D O I：

10.3389/fcell.2020.00260

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Endothelial to mesenchymal transition (EndMT) is a complex biological process that gives rise to cells with multipotent potential. EndMT is essential for the formation of the cardiovascular system during embryonic development. Emerging results link EndMT to the postnatal onset and progression of fibrotic diseases and cancer. Moreover, recent reports have emphasized the potential for EndMT in tissue engineering and regenerative applications by regulating the differentiation status of cells. Transforming growth factor beta (TGF-beta) engages in many important physiological processes and is a potent inducer of EndMT. In this review, we first summarize the mechanisms of the TGF-beta signaling pathway as it relates to EndMT. Thereafter, we discuss the pivotal role of TGF-beta-induced EndMT in the development of cardiovascular diseases, fibrosis, and cancer, as well as the potential application of TGF-beta-induced EndMT in tissue engineering.

引用

页数：14

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