Collagen receptor cross-talk determines ?-smooth muscle actin-dependent collagen gene expression in angiotensin II-stimulated cardiac fibroblasts.

ABSTRACT: Excessive collagen deposition by myofibroblasts during adverse cardiac remodeling leads to myocardial fibrosis that can compromise cardiac function. Unraveling the mechanisms underlying collagen gene expression in cardiac myofibroblasts is therefore an important clinical goal. The collagen receptors, discoidin domain receptor 2 (DDR2), a collagen-specific receptor tyrosine kinase, and integrin-?1, are reported to mediate tissue fibrosis. Here, we probed the role of DDR2-integrin-?1 cross-talk in the regulation of collagen ?1(I) gene expression in angiotensin II (Ang II)-stimulated cardiac fibroblasts. Results from gene silencing/overexpression approaches, electrophoretic mobility shift assays, and ChIP revealed that DDR2 acts via extracellular signal-regulated kinase 1/2 mitogen-activated protein kinase (ERK1/2 MAPK)-dependent transforming growth factor-?1 (TGF-?1) signaling to activate activator protein-1 (AP-1) that in turn transcriptionally enhances the expression of collagen-binding integrin-?1 in Ang II-stimulated cardiac fibroblasts. The DDR2-integrin-?1 link was also evident in spontaneously hypertensive rats and DDR2-knockout mice. Further, DDR2 acted via integrin-?1 to regulate ?-smooth muscle actin (?-SMA) and collagen type I expression in Ang II-exposed cardiac fibroblasts. Downstream of the DDR2-integrin-?1 axis, ?-SMA was found to regulate collagen ?1(I) gene expression via the Ca2+ channel, transient receptor potential cation channel subfamily C member 6 (TRPC6), and the profibrotic transcription factor, Yes-associated protein (YAP). This finding indicated that fibroblast-to-myofibroblast conversion is mechanistically coupled to collagen expression. The observation that collagen receptor cross-talk underlies ?-SMA-dependent collagen type I expression in cardiac fibroblasts expands our understanding of the complex mechanisms involved in collagen gene expression in the heart and may be relevant to cardiac fibrogenesis.

SUBMITTER: V H 

PROVIDER: S-EPMC6926455 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature