The Angiotensin AT2 Receptor: From a Binding Site to a Novel Therapeutic TargetShow others and affiliations
2022 (English)In: Pharmacological Reviews, ISSN 0031-6997, E-ISSN 1521-0081, Vol. 74, no 4, p. 1051-1135Article, review/survey (Refereed) Published
Abstract [en]
Discovered more than 30 years ago, the angiotensin AT2 receptor (AT2R) has evolved from a binding site with unknown function to a firmly established major effector within the protective arm of the renin-angiotensin system (RAS) and a target for new drugs in development. The AT2R represents an endogenous protective mechanism that can be manipulated in the majority of preclinical models to alleviate lung, renal, cardiovascular, metabolic, cutaneous, and neural diseases as well as cancer. This article is a comprehensive review summarizing our current knowledge of the AT2R, from its discovery to its position within the RAS and its overall functions. This is followed by an in-depth look at the characteristics of the AT2R, including its structure, intracellular signaling, homo- and heterodimerization, and expression. AT2R-selective ligands, from endogenous peptides to synthetic peptides and nonpeptide molecules that are used as research tools, are discussed. Finally, we summarize the known physiological roles of the AT2R and its abundant protective effects in multiple experimental disease models and expound on AT2R ligands that are undergoing development for clinical use. The present review highlights the controversial aspects and gaps in our knowledge of this receptor and illuminates future perspectives for AT2R research.
Place, publisher, year, edition, pages
American Society for Pharmacology & Experimental Therapeutics (ASPET) , 2022. Vol. 74, no 4, p. 1051-1135
National Category
Pharmacology and Toxicology
Identifiers
URN: urn:nbn:se:uu:diva-500697DOI: 10.1124/pharmrev.120.000281ISI: 000958588300007PubMedID: 36180112OAI: oai:DiVA.org:uu-500697DiVA, id: diva2:1752344
Funder
NIH (National Institutes of Health)Novo Nordisk, NNF19OC00585922023-04-212023-04-212023-04-21Bibliographically approved