The TGFβ superfamily in cardiac dysfunction
Author(s) -
Jian Wu,
Olan JacksonWeaver,
Jian Xu
Publication year - 2018
Publication title -
acta biochimica et biophysica sinica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.771
H-Index - 57
eISSN - 1745-7270
pISSN - 1672-9145
DOI - 10.1093/abbs/gmy007
Subject(s) - bone morphogenetic protein , growth differentiation factor , transforming growth factor , angiogenesis , cardiac fibrosis , transforming growth factor beta , bone morphogenetic protein 2 , microbiology and biotechnology , fibrosis , biology , myofibroblast , cancer research , endocrinology , medicine , genetics , gene , in vitro
TGFβ superfamily includes the transforming growth factor βs (TGFβs), bone morphogenetic proteins (BMPs), growth and differentiation factors (GDFs) and Activin/Inhibin families of ligands. Among the 33 members of TGFβ superfamily ligands, many act on multiple types of cells within the heart, including cardiomyocytes, cardiac fibroblasts/myofibroblasts, coronary endothelial cells, smooth muscle cells, and immune cells (e.g. monocytes/macrophages and neutrophils). In this review, we highlight recent discoveries on TGFβs, BMPs, and GDFs in different cardiac residential cellular components, in association with functional impacts in heart development, injury repair, and dysfunction. Specifically, we will review the roles of TGFβs, BMPs, and GDFs in cardiac hypertrophy, fibrosis, contractility, metabolism, angiogenesis, and regeneration.
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