AI Article Synopsis

  • G protein-coupled receptors (GPCRs) can activate cellular signaling through G proteins or β-arrestins, but the angiotensin II analog [Sarcosine1Ile4Ile8]-angiotensin II (SII) fails to activate G proteins in real physiological settings, instead relying on β-arrestin-2 for signaling.
  • Research shows that SII and other ligands displayed different signaling outcomes depending on the concentration of AT1R, with β-arrestin-biased ligands only showing effective signaling at higher receptor levels.
  • The findings suggest that overexpressing AT1R can distort the perceived signaling bias of GPCR ligands, indicating caution in using overexpression models to study

Article Abstract

G protein-coupled receptors (GPCRs) regulate cellular signaling pathways by coupling to two classes of transducers: heterotrimeric G proteins and β-arrestins. [Sarcosine1Ile4Ile8]-angiotensin II (SII), an analog of the endogenous ligand angiotensin II (AngII) for the angiotensin II type 1 receptor (AT1R), fails to activate G protein in physiologically relevant models. Despite this, SII and several derivatives induce cellular signaling outcomes through β-arrestin-2-dependent mechanisms. However, studies reliant on exogenous AT1R overexpression indicate that SII is a partial agonist for G protein signaling and lacks β-arrestin-exclusive functional specificity. We investigated this apparent discrepancy by profiling changes in functional specificity at increasing expression levels of AT1R using a stably integrated tetracycline-titratable expression system stimulated with AngII, SII, and four other AngII analogs displaying different signaling biases. Unbiased and G protein-biased ligands activated dose-dependent calcium responses at all tested receptor concentrations. In contrast, β-arrestin-biased ligands induced dose-dependent calcium signaling only at higher AT1R overexpression levels. Using inhibitors of G proteins, we demonstrated that both Gi and Gq/11 mediated overexpression-dependent calcium signaling by β-arrestin-biased ligands. Regarding β-arrestin-mediated cellular events, the β-arrestin-biased ligand TRV026 induced receptor internalization at low physiological receptor levels insufficient for it to initiate calcium signaling. In contrast, unbiased AngII exhibited no relative preference between these outcomes under such low receptor conditions. However, with high receptor overexpression, TRV026 lost its functional selectivity. These results suggest receptor overexpression misleadingly distorts the bias of AT1R ligands and highlight the risks of using overexpressed systems to infer the signaling bias of GPCR ligands in physiologically relevant contexts.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10038289PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0283477PLOS

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