| Literature DB >> 36068469 |
Jordana I Borges1, Alexandra M Carbone1, Natalie Cora1, Anastasiya Sizova1, Anastasios Lymperopoulos2.
Abstract
α2-Adrenergic receptors (ARs) mediate many cellular actions of epinephrine and norepinephrine, including inhibition of their secretion (sympathetic inhibition) from adrenal chromaffin cells. Like many other G protein-coupled receptors (GPCRs), they undergo agonist-dependent phosphorylation and desensitization by GPCR kinases (GRKs), a phenomenon recently shown to play a major role in the sympathetic overdrive that accompanies and aggravates chronic heart failure. A three-glutamic acid deletion polymorphism in the human α2B-AR subtype gene (Glu301-303) causes impaired agonist-promoted receptor phosphorylation and desensitization, resulting in enhanced signaling to inhibition of cholinergic-induced catecholamine secretion in adrenal chromaffin cells. One of the various pharmacological assays that can be used to quantify and quantitatively compare the degrees of agonist-dependent desensitization, i.e., G protein decoupling, of these two polymorphic α2B-AR variants (or of any two GPCRs for that matter) is the guanosine-5'-O-3-thiotriphosphate (GTPγS) assay that can directly quantify heterotrimeric G protein activation.Entities:
Keywords: Agonist-dependent desensitization; G protein-coupled receptor; GTPγS assay; Heterotrimeric G protein; Polymorphic α2B-adrenergic receptor; Signal transduction
Mesh:
Substances:
Year: 2022 PMID: 36068469 DOI: 10.1007/978-1-0716-2573-6_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745