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RAS Proteins and Their Regulators in Human Disease.人类疾病中的RAS蛋白及其调节因子
Cell. 2017 Jun 29;170(1):17-33. doi: 10.1016/j.cell.2017.06.009.
2
Methodological advances: the unsung heroes of the GPCR structural revolution.方法学进展:GPCR 结构革命的无名英雄。
Nat Rev Mol Cell Biol. 2015 Feb;16(2):69-81. doi: 10.1038/nrm3933. Epub 2015 Jan 15.
3
Circulating follicular helper-like T cells in systemic lupus erythematosus: association with disease activity.循环滤泡辅助样 T 细胞在系统性红斑狼疮中的作用:与疾病活动的相关性。
Arthritis Rheumatol. 2015 Apr;67(4):988-99. doi: 10.1002/art.39020.
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G protein-coupled receptor mutations and human genetic disease.G蛋白偶联受体突变与人类遗传疾病。
Methods Mol Biol. 2014;1175:153-87. doi: 10.1007/978-1-4939-0956-8_8.
5
The deficiency of Gαq leads to enhanced T-cell survival.Gαq的缺乏导致T细胞存活率提高。
Immunol Cell Biol. 2014 Oct;92(9):781-90. doi: 10.1038/icb.2014.53. Epub 2014 Jun 24.
6
Chemokine (C-X-C motif) ligand (CXCL)10 in autoimmune diseases.趋化因子(C-X-C 基序)配体(CXCL)10 在自身免疫性疾病中的作用。
Autoimmun Rev. 2014 Mar;13(3):272-80. doi: 10.1016/j.autrev.2013.10.010. Epub 2013 Nov 2.
7
CCR5-Delta32: implications in SLE development.CCR5-Delta32:在系统性红斑狼疮发病机制中的意义。
Int J Immunogenet. 2014 Jun;41(3):236-41. doi: 10.1111/iji.12094. Epub 2013 Oct 29.
8
The regulating function of heterotrimeric G proteins in the immune system.异三聚体 G 蛋白在免疫系统中的调节功能。
Arch Immunol Ther Exp (Warsz). 2013 Aug;61(4):309-19. doi: 10.1007/s00005-013-0230-5. Epub 2013 Apr 7.
9
Gαq gene promoter polymorphisms and rheumatoid arthritis in the Han Chinese population are not associated.汉族人群中Gαq基因启动子多态性与类风湿关节炎不相关。
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10
G protein-coupled receptors--recent advances.G蛋白偶联受体——最新进展
Acta Biochim Pol. 2012;59(4):515-29. Epub 2012 Dec 18.

G蛋白:健康与疾病中的二元开关

G proteins: binary switches in health and disease.

作者信息

Afzal Muhammad Sohail

机构信息

Department of Life Sciences, School of Science, University of Management and Technology (UMT), Lahore, Pakistan.

出版信息

Cent Eur J Immunol. 2020;45(3):364-367. doi: 10.5114/ceji.2020.101271. Epub 2020 Nov 1.

DOI:10.5114/ceji.2020.101271
PMID:33437192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7789995/
Abstract

Cell signaling plays critical role in health and disease. The normal functioning of body depends on the homeostasis of immunity players. One of the very important cell signaling participants is G protein-coupled receptor (GPCR). GPCRs transduce extracellular signals into target cell by binding to and activating different G proteins (G , families Gi, Gs, Gq/11, G12/13) leading to range of different functions. Abnormal GPCRs signaling leads to various abnormalities, including but not limited to, cancer, pain, cardiac problems, and asthma. Mutations, which lead to activation or inactivation of GPCR pathways, permanently alter the pathways controlled by these receptors. A large number of human cancer incidence is a consequence of genetic abnormalities in signaling pathways, which influence cell division. Some bacteria and pathogens may interfere with the GPCR signaling pathways for their survival and immune evasion. Inhibition of GPCR signaling by small inhibitors is a novel way to treat various pathological conditions. There are several types of GPCRs in human genome, which due to their central role in health and disease, are the target of many commercially available drugs. Importantly, GPCRs have huge impact on drug discovery and approximately 30% of current drug targets are GPCRs. There is a need of further studies to explore more the role of G protein and the GPCRs in human health and how certain mutations can lead to disease state. Such studies may be important to adjust the signaling pathways for health improvement.

摘要

细胞信号传导在健康和疾病中起着关键作用。身体的正常功能依赖于免疫相关分子的稳态。G蛋白偶联受体(GPCR)是非常重要的细胞信号传导参与者之一。GPCR通过与不同的G蛋白(Gα家族,包括Gi、Gs、Gq/11、G12/13)结合并激活,将细胞外信号转导至靶细胞,从而导致一系列不同的功能。GPCR信号异常会导致各种异常情况,包括但不限于癌症、疼痛、心脏问题和哮喘。导致GPCR信号通路激活或失活的突变会永久性地改变这些受体所控制的信号通路。大量人类癌症的发生是信号通路中基因异常的结果,这些异常影响细胞分裂。一些细菌和病原体可能会干扰GPCR信号通路以实现其生存和免疫逃逸。用小分子抑制剂抑制GPCR信号传导是治疗各种病理状况的一种新方法。人类基因组中有几种类型的GPCR,由于它们在健康和疾病中的核心作用,是许多市售药物的靶点。重要的是,GPCR对药物研发有巨大影响,目前约30%的药物靶点是GPCR。需要进一步研究以更深入地探索G蛋白和GPCR在人类健康中的作用,以及某些突变如何导致疾病状态。此类研究对于调整信号通路以改善健康可能很重要。