1. Academic Validation
  2. Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas

Angiotensin-(1-7) is an endogenous ligand for the G protein-coupled receptor Mas

  • Proc Natl Acad Sci U S A. 2003 Jul 8;100(14):8258-63. doi: 10.1073/pnas.1432869100.
Robson A S Santos 1 Ana C Simoes e Silva Christine Maric Denise M R Silva Raquel Pillar Machado Insa de Buhr Silvia Heringer-Walther Sergio Veloso B Pinheiro Myriam Teresa Lopes Michael Bader Elizabeth P Mendes Virgina Soares Lemos Maria Jose Campagnole-Santos Heinz-Peter Schultheiss Robert Speth Thomas Walther
Affiliations

Affiliation

  • 1 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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