代谢物感知G蛋白偶联受体-饮食相关免疫调节的促进者。

IF 26.9 1区 医学 Q1 IMMUNOLOGY
Jian K Tan, Craig McKenzie, Eliana Mariño, Laurence Macia, Charles R Mackay
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引用次数: 198

摘要

营养和肠道微生物组调节许多系统,包括免疫系统、代谢系统和神经系统。我们认为,宿主对饮食和细菌代谢物的缺乏(或充足)以动态的方式作出反应,以优化反应和生存。G蛋白偶联受体(gpcr)家族被称为代谢物感应gpcr结合各种代谢物并传递对适当的免疫和代谢功能很重要的信号。该家族的成员包括GPR43、GPR41、GPR109A、GPR120、GPR40、GPR84、GPR35和GPR91。此外,胆汁酸受体如GPR131 (TGR5)和质子感应受体如GPR65也表现出类似的特征。这个gpcr家族的一个一贯特征是它们提供抗炎信号;许多还调节新陈代谢和肠道平衡。这些受体代表了肠道微生物组影响脊椎动物生理的主要机制之一,它们也提供了免疫系统和代谢系统之间的联系。通过一种或多种这些代谢物感应gpcr的信号传导不足可能导致人类疾病,如哮喘、食物过敏、1型和2型糖尿病、肝脂肪变性、心血管疾病和炎症性肠病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolite-Sensing G Protein-Coupled Receptors-Facilitators of Diet-Related Immune Regulation.
Nutrition and the gut microbiome regulate many systems, including the immune, metabolic, and nervous systems. We propose that the host responds to deficiency (or sufficiency) of dietary and bacterial metabolites in a dynamic way, to optimize responses and survival. A family of G protein-coupled receptors (GPCRs) termed the metabolite-sensing GPCRs bind to various metabolites and transmit signals that are important for proper immune and metabolic functions. Members of this family include GPR43, GPR41, GPR109A, GPR120, GPR40, GPR84, GPR35, and GPR91. In addition, bile acid receptors such as GPR131 (TGR5) and proton-sensing receptors such as GPR65 show similar features. A consistent feature of this family of GPCRs is that they provide anti-inflammatory signals; many also regulate metabolism and gut homeostasis. These receptors represent one of the main mechanisms whereby the gut microbiome affects vertebrate physiology, and they also provide a link between the immune and metabolic systems. Insufficient signaling through one or more of these metabolite-sensing GPCRs likely contributes to human diseases such as asthma, food allergies, type 1 and type 2 diabetes, hepatic steatosis, cardiovascular disease, and inflammatory bowel diseases.
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来源期刊
Annual review of immunology
Annual review of immunology 医学-免疫学
CiteScore
57.20
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Immunology, in publication since 1983, focuses on basic immune mechanisms and molecular basis of immune diseases in humans. Topics include innate and adaptive immunity; immune cell development and differentiation; immune control of pathogens (viruses, bacteria, parasites) and cancer; and human immunodeficiency and autoimmune diseases. The current volume of this journal has been converted from gated to open access through Annual Reviews' Subscribe to Open program, with all articles published under a CC BY license.
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