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Free keywords:
INTEGRIN ACTIVATION; MYOSIN-II; FIBRONECTIN; TALIN; EXPRESSION;
ADHESOME; BETA(1); IDENTIFICATION; CRISPR-CAS9; DYNAMICS
Abstract:
Haematopoietic cells and platelets employ G-protein-coupled receptors (GPCRs) to sense extracellular information and respond by initiating integrin-mediated adhesion. So far, such processes have not been demonstrated in non-haematopoietic cells. Here, we report that the activation of protease-activated receptors PAR1 and PAR2 induce multiple signalling pathways to establish alpha(5)beta(1)-integrin-mediated adhesion. First, PARs signal via G beta gamma and PI3K to alpha(5)beta(1)-integrins to adopt a talin- and kindlin-dependent high-affinity conformation, which triggers fibronectin binding and initiates cell adhesion. Then, within 60 s, PARs signal via G alpha(13), G alpha(i), ROCK and Src to strengthen the alpha(5)beta(1)-integrin-mediated adhesion. Furthermore, PAR signalling changes the abundance of numerous proteins in the adhesome assembled by alpha(5)beta(1)-integrins, including G alpha(13), vacuolar protein-sorting-associated protein 36, and band 4.1-like protein 4B or 5, and accelerates cell adhesion maturation, spreading and migration. The mechanistic insights describe how agonist binding to PAR employs GPCR and integrin-signalling pathways to initiate and regulate adhesion and to guide physiological responses of non-haematopoietic cells.
As in haematopoietic cells and platelets, agonist binding to protease-activated receptors PAR1 and PAR2 in non-haematopoietic cells also triggers signalling pathways that lead to alpha(5)beta(1)-integrin-mediated cell adhesion.
