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在过表达系统中,G 蛋白偶联受体的偏向信号丧失。

Loss of biased signaling at a G protein-coupled receptor in overexpressed systems.

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina, United States of America.

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina, United States of America.

出版信息

PLoS One. 2023 Mar 24;18(3):e0283477. doi: 10.1371/journal.pone.0283477. eCollection 2023.

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.

摘要

G 蛋白偶联受体 (GPCR) 通过与两类转导蛋白偶联来调节细胞信号通路:异三聚体 G 蛋白和β-arrestin。[Sarcosine1Ile4Ile8]-angiotensin II (SII) 是血管紧张素 II 型 1 受体 (AT1R) 的内源性配体血管紧张素 II 的类似物,在生理相关模型中无法激活 G 蛋白。尽管如此,SII 和几种衍生物仍通过β-arrestin-2 依赖性机制诱导细胞信号转导。然而,依赖于外源性 AT1R 过表达的研究表明,SII 是 G 蛋白信号的部分激动剂,缺乏β-arrestin 特有的功能特异性。我们通过使用四环素可滴定表达系统在增加 AT1R 表达水平的情况下对功能特异性的变化进行分析,从而研究了这种明显的差异,该系统受到 AngII、SII 和其他四种显示不同信号转导偏向的 AngII 类似物的刺激。在所有测试的受体浓度下,无偏和 G 蛋白偏向配体均激活了剂量依赖性的钙反应。相比之下,β-arrestin 偏向配体仅在更高的 AT1R 过表达水平下诱导剂量依赖性的钙信号。使用 G 蛋白抑制剂,我们证明了 Gq/11 介导了β-arrestin 偏向配体引起的过表达依赖性钙信号。关于β-arrestin 介导的细胞事件,β-arrestin 偏向配体 TRV026 在低生理受体水平下诱导受体内化,该水平不足以引发钙信号。相比之下,无偏的 AngII 在如此低的受体条件下,对这些结果没有相对偏好。然而,随着受体过表达,TRV026 失去了其功能选择性。这些结果表明,受体过表达错误地扭曲了 AT1R 配体的偏向性,并强调了在生理相关背景下使用过表达系统推断 GPCR 配体的信号偏向性的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4809/10038289/1b8c7c372daf/pone.0283477.g001.jpg

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