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Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas
Authors:Santos Robson A S  Simoes e Silva Ana C  Maric Christine  Silva Denise M R  Machado Raquel Pillar  de Buhr Insa  Heringer-Walther Silvia  Pinheiro Sergio Veloso B  Lopes Myriam Teresa  Bader Michael  Mendes Elizabeth P  Lemos Virgina Soares  Campagnole-Santos Maria Jose  Schultheiss Heinz-Peter  Speth Robert  Walther Thomas
Institution:Department of Physiology and Biophysics, Federal University of Minas Gerais, Belo Horizonte, 31270, Minas Gerais, Brazil.
Abstract:The renin-angiotensin system plays a critical role in blood pressure control and body fluid and electrolyte homeostasis. Besides angiotensin (Ang) II, other Ang peptides, such as Ang III Ang-(2-8)], Ang IV Ang-(3-8)], and Ang-(1-7) may also have important biological activities. Ang-(1-7) has become an angiotensin of interest in the past few years, because its cardiovascular and baroreflex actions counteract those of Ang II. Unique angiotensin-binding sites specific for this heptapeptide and studies with a selective Ang-(1-7) antagonist indicated the existence of a distinct Ang-(1-7) receptor. We demonstrate that genetic deletion of the G protein-coupled receptor encoded by the Mas protooncogene abolishes the binding of Ang-(1-7) to mouse kidneys. Accordingly, Mas-deficient mice completely lack the antidiuretic action of Ang-(1-7) after an acute water load. Ang-(1-7) binds to Mas-transfected cells and elicits arachidonic acid release. Furthermore, Mas-deficient aortas lose their Ang-(1-7)-induced relaxation response. Collectively, these findings identify Mas as a functional receptor for Ang-(1-7) and provide a clear molecular basis for the physiological actions of this biologically active peptide.
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