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G蛋白偶联受体在缺氧介导信号传导中作用的最新进展

Recent Advances on the Role of G Protein-Coupled Receptors in Hypoxia-Mediated Signaling.

作者信息

Lappano Rosamaria, Rigiracciolo Damiano, De Marco Paola, Avino Silvia, Cappello Anna Rita, Rosano Camillo, Maggiolini Marcello, De Francesco Ernestina Marianna

机构信息

Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, Via Bucci, 87036, Rende, CS, Italy.

UOS Proteomics IRCCS AOU San Martino-IST National Institute for Cancer Research, Largo R. Benzi 10, 16132, Genoa, Italy.

出版信息

AAPS J. 2016 Mar;18(2):305-10. doi: 10.1208/s12248-016-9881-6. Epub 2016 Feb 10.

DOI:10.1208/s12248-016-9881-6
PMID:26865461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4779097/
Abstract

G protein-coupled receptors (GPCRs) are cell surface proteins mainly involved in signal transmission; however, they play a role also in several pathophysiological conditions. Chemically heterogeneous molecules like peptides, hormones, lipids, and neurotransmitters activate second messengers and induce several biological responses by binding to these seven transmembrane receptors, which are coupled to heterotrimeric G proteins. Recently, additional molecular mechanisms have been involved in GPCR-mediated signaling, leading to an intricate network of transduction pathways. In this regard, it should be mentioned that diverse GPCR family members contribute to the adaptive cell responses to low oxygen tension, which is a distinguishing feature of several illnesses like neoplastic and cardiovascular diseases. For instance, the G protein estrogen receptor, namely G protein estrogen receptor (GPER)/GPR30, has been shown to contribute to relevant biological effects induced by hypoxia via the hypoxia-inducible factor (HIF)-1α in diverse cell contexts, including cancer. Likewise, GPER has been found to modulate the biological outcome of hypoxic/ischemic stress in both cardiovascular and central nervous systems. Here, we describe the role exerted by GPCR-mediated signaling in low oxygen conditions, discussing, in particular, the involvement of GPER by a hypoxic microenvironment.

摘要

G蛋白偶联受体(GPCRs)是主要参与信号传导的细胞表面蛋白;然而,它们在多种病理生理状况中也发挥作用。肽、激素、脂质和神经递质等化学性质各异的分子通过与这些与异源三聚体G蛋白偶联的七跨膜受体结合,激活第二信使并诱导多种生物学反应。最近,其他分子机制也参与了GPCR介导的信号传导,形成了一个复杂的转导途径网络。在这方面,应该提到的是,不同的GPCR家族成员有助于细胞对低氧张力的适应性反应,这是肿瘤和心血管疾病等多种疾病的一个显著特征。例如,G蛋白雌激素受体,即G蛋白雌激素受体(GPER)/GPR30,已被证明在包括癌症在内的多种细胞环境中,通过缺氧诱导因子(HIF)-1α,对缺氧诱导的相关生物学效应有贡献。同样,已发现GPER在心血管系统和中枢神经系统中均能调节缺氧/缺血应激的生物学结果。在此,我们描述了GPCR介导的信号传导在低氧条件下所发挥的作用,尤其讨论了缺氧微环境对GPER的影响。

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本文引用的文献

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GPER is involved in the stimulatory effects of aldosterone in breast cancer cells and breast tumor-derived endothelial cells.G蛋白偶联雌激素受体(GPER)参与醛固酮对乳腺癌细胞和乳腺肿瘤来源的内皮细胞的刺激作用。
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HIF hydroxylase pathways in cardiovascular physiology and medicine.心血管生理学与医学中的低氧诱导因子羟化酶途径。
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Activation of novel estrogen receptor GPER results in inhibition of cardiocyte apoptosis and cardioprotection.新型雌激素受体GPER的激活导致心肌细胞凋亡的抑制和心脏保护作用。
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