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 language | American English |
|---|---|
| Pages (from-to) | 8258-8263 |
| Number of pages | 6 |
| Journal | Proceedings of the National Academy of Sciences (PNAS) |
| Volume | 100 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 8 2003 |
| Externally published | Yes |
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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