肥大细胞活化中mass相关G蛋白偶联受体x2的配体和信号传导。

2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Yan-Ni Mi, Na-Na Ping, Yong-Xiao Cao
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引用次数: 7

摘要

肥大细胞相关G蛋白偶联受体x2 (MRGPRX2)被认为是一种激活肥大细胞(MCs)的新型受体。MRGPRX2具有促进mc依赖性宿主防御和免疫调节的双重作用,参与假性过敏药物反应、疼痛、瘙痒和炎症性疾病的发病机制。在本文中,我们讨论了MRGPRX2介导MCs激活的可能信号通路,并对MRGPRX2在MCs激活中的激动剂和抑制剂进行了总结和分类。MRGPRX2是一种低亲和力和低选择性受体,这使得它可以与多种配体相互作用。多种MRGPRX2配体利用其跨膜结构域的保守残基和羧基端Ser/Thr残基进行配体结合和G蛋白偶联。这种偶联可能启动磷酸化级联,诱导Ca2+动员,并通过MAPK和NF-κB途径引起脱颗粒和细胞因子和趋化因子的产生,从而导致MCs活化。MRGPRX2对MCs的激动剂分为多肽(包括抗菌肽、神经肽、MCs脱粒肽、肽激素)和非多肽(包括fda批准的药物)。MRGPRX2的抑制剂包括非选择性GPCR抑制剂、草药提取物、小分子MRGPRX2拮抗剂和DNA适体药物。筛选和分类MRGPRX2配体,总结其信号通路,有助于我们进一步了解MRGPRX2介导的MCs生理和病理作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ligands and Signaling of Mas-Related G Protein-Coupled Receptor-X2 in Mast Cell Activation.

Mas-related G protein-coupled receptor-X2 (MRGPRX2) is known as a novel receptor to activate mast cells (MCs). MRGPRX2 plays a dual role in promoting MC-dependent host defense and immunomodulation and contributing to the pathogenesis of pseudo-allergic drug reactions, pain, itching, and inflammatory diseases. In this article, we discuss the possible signaling pathways of MCs activation mediated by MRGPRX2 and summarize and classify agonists and inhibitors of MRGPRX2 in MCs activation. MRGPRX2 is a low-affinity and low-selectivity receptor, which allows it to interact with a diverse group of ligands. Diverse MRGPRX2 ligands utilize conserved residues in its transmembrane (TM) domains and carboxyl-terminus Ser/Thr residues to undergo ligand binding and G protein coupling. The coupling likely initiates phosphorylation cascades, induces Ca2+ mobilization, and causes degranulation and generation of cytokines and chemokines via MAPK and NF-κB pathways, resulting in MCs activation. Agonists of MRGPRX2 on MCs are divided into peptides (including antimicrobial peptides, neuropeptides, MC degranulating peptides, peptide hormones) and nonpeptides (including FDA-approved drugs). Inhibitors of MRGPRX2 include non-selective GPCR inhibitors, herbal extracts, small-molecule MRGPRX2 antagonists, and DNA aptamer drugs. Screening and classifying MRGPRX2 ligands and summarizing their signaling pathways would improve our understanding of MRGPRX2-mediated physiological and pathological effects on MCs.

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来源期刊
Reviews of Physiology Biochemistry and Pharmacology
Reviews of Physiology Biochemistry and Pharmacology 医学-生化与分子生物学
CiteScore
11.40
自引率
0.00%
发文量
5
审稿时长
>12 weeks
期刊介绍: The highly successful Reviews of Physiology, Biochemistry and Pharmacology continue to offer high-quality, in-depth reviews covering the full range of modern physiology, biochemistry and pharmacology. Leading researchers are specially invited to provide a complete understanding of the key topics in these archetypal multidisciplinary fields. In a form immediately useful to scientists, this periodical aims to filter, highlight and review the latest developments in these rapidly advancing fields.
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