Regulation of the extracellular signal-regulated kinase pathway in adult myocardium: differential roles of G q/11, G i and G 12/13 proteins in signalling by α 1-adrenergic, endothelin-1 and thrombin-sensitive protease-activated receptors

Abstract

Using adenoviruses encoding RGS2, RGS4 and Lsc (regulator of G protein signalling (RGS) domain of p115 RhoGEF), we investigated the contributions of G q/11, G i and G 12/13 proteins to G protein-coupled receptor (GPCR)-mediated activation of the extracellular signal-regulated kinase (ERK) pathway in adult rat ventricular myocytes (ARVM). Exposure to phenylephrine, endothelin-1 (ET-1) or thrombin induced significant activation of ERK1/2 and their downstream target 90 kDa ribosomal S6 kinase (p90 RSK), which was abolished by overexpression of RGS4 (inhibits signalling via G q/11 and G i) or RGS2 (inhibits signalling via G q/11). Pertussis toxin (inhibits signalling via G i) only partially attenuated the activation of ERK1/2 and p90 RSK by phenylephrine and ET-1, but abolished such activation by thrombin. Overexpression of Lsc (inhibits signalling via G 12/13) did not affect the responses to phenylephrine and ET-1, but suppressed the activation of ERK1/2 and p90 RSK by thrombin. We conclude that full activation of the ERK pathway in ARVM by α 1-adrenergic, ET-1 and thrombin receptors requires the activation of distinct families of heterotrimeric G proteins.