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

  • Robson A Santos
  • , Ana C Simoes e Silva
  • , Christine Maric
  • , Denise M Silva
  • , Raquel Pillar Machado
  • , Insa de Buhr
  • , Silvia Heringer-Walther
  • , Sergio Veloso Pinheiro
  • , Myriam Teresa Lopes
  • , Michael Bader
  • , Elizabeth P Mendes
  • , Virgina Soares Lemos
  • , Maria Jose Campagnole-Santos
  • , Heinz-Peter Schultheiss
  • , Robert Speth
  • , Thomas Walther

Research output: Contribution to journal › Article › peer-review

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.

Original languageAmerican English
Pages (from-to)8258-8263
Number of pages6
JournalProceedings of the National Academy of Sciences (PNAS)
Volume100
Issue number14
DOIs
StatePublished - Jul 8 2003
Externally publishedYes

Funding

This work was supported in part by a Deutscher Akademischer Austauschdienst/Comissao de Aperfeiçoamento de Pessoal de Nival Superior PROBRAL project, Financiadora de Estudos e Projetos-Conselho Nacional de Pesquisas PRONEX, and a grant of the Humboldt Foundation (to S.H.-W.).

Keywords

  • Angiotensin I/antagonists & inhibitors
  • Animals
  • Aorta/drug effects
  • Arachidonic Acid/metabolism
  • CHO Cells
  • COS Cells
  • Chlorocebus aethiops
  • Cricetinae
  • Cricetulus
  • Diuresis/drug effects
  • Kidney/metabolism
  • Ligands
  • Mice
  • Mice, Knockout
  • Peptide Fragments/antagonists & inhibitors
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins/deficiency
  • Receptors, G-Protein-Coupled
  • Recombinant Fusion Proteins/physiology
  • Transfection
  • Vasodilation/drug effects
  • Binding
  • Renin angiotensin system
  • Mas protooncogene

Disciplines

  • Medicine and Health Sciences
  • Pharmacy and Pharmaceutical Sciences

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