PAR1 Scaffolds TGF?RII to Downregulate TGF-? Signaling and Activate ESC Differentiation to Endothelial Cells.

ABSTRACT: We studied the function of the G-protein-coupled receptor PAR1 in mediating the differentiation of mouse embryonic stem cells (mESCs) to endothelial cells (ECs) that are capable of inducing neovascularization. We observed that either deletion or activation of PAR1 suppressed mouse embryonic stem cell (mESC) differentiation to ECs and neovascularization in mice. This was mediated by induction of TGF?RII/TGF?RI interaction, forming an active complex, which in turn induced SMAD2 phosphorylation. Inhibition of TGF-? signaling in PAR1-deficient mESCs restored the EC differentiation potential of mESCs. Thus, PAR1 in its inactive unligated state functions as a scaffold for TGF?RII to downregulate TGF-? signaling, and thereby promote ESC transition to functional ECs. The PAR1 scaffold function in ESCs is an essential mechanism for dampening TGF-? signaling and regulating ESC differentiation.

SUBMITTER: Gong H 

PROVIDER: S-EPMC5161529 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature