Literature DB >> 33479839

Ligands and Signaling of Mas-Related G Protein-Coupled Receptor-X2 in Mast Cell Activation.

Yan-Ni Mi1, Na-Na Ping2, Yong-Xiao Cao3.   

Abstract

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.

Entities:  

Keywords:  Agonist; Antagonist; Degranulation; Generation of cytokines and chemokines; Host defense; Inflammatory diseases; Inhibitors; Mas-related G protein-coupled receptor-X2; Mast cells; Pseudo-allergic drug reactions

Year:  2021        PMID: 33479839     DOI: 10.1007/112_2020_53

Source DB:  PubMed          Journal:  Rev Physiol Biochem Pharmacol        ISSN: 0303-4240            Impact factor:   5.545


  172 in total

1.  Naturally Occurring Missense MRGPRX2 Variants Display Loss of Function Phenotype for Mast Cell Degranulation in Response to Substance P, Hemokinin-1, Human β-Defensin-3, and Icatibant.

Authors:  Ibrahim Alkanfari; Kshitij Gupta; Tahsin Jahan; Hydar Ali
Journal:  J Immunol       Date:  2018-05-23       Impact factor: 5.422

2.  MRGPRX2 is negatively targeted by SCF and IL-4 to diminish pseudo-allergic stimulation of skin mast cells in culture.

Authors:  Magda Babina; Zhao Wang; Metin Artuc; Sven Guhl; Torsten Zuberbier
Journal:  Exp Dermatol       Date:  2018-09-03       Impact factor: 3.960

3.  Dual action of neurokinin-1 antagonists on Mas-related GPCRs.

Authors:  Ehsan Azimi; Vemuri B Reddy; Kai-Ting C Shade; Robert M Anthony; Sebastien Talbot; Paula Juliana Seadi Pereira; Ethan A Lerner
Journal:  JCI Insight       Date:  2016-10-06

4.  Activation of the inhibitory GTP-binding protein of adenylate cyclase, Gi, by beta-adrenergic receptors in reconstituted phospholipid vesicles.

Authors:  T Asano; T Katada; A G Gilman; E M Ross
Journal:  J Biol Chem       Date:  1984-08-10       Impact factor: 5.157

Review 5.  Emerging Roles for MAS-Related G Protein-Coupled Receptor-X2 in Host Defense Peptide, Opioid, and Neuropeptide-Mediated Inflammatory Reactions.

Authors:  Hydar Ali
Journal:  Adv Immunol       Date:  2017-07-24       Impact factor: 5.324

6.  Allergic FcεRI- and pseudo-allergic MRGPRX2-triggered mast cell activation routes are independent and inversely regulated by SCF.

Authors:  M Babina; S Guhl; M Artuc; T Zuberbier
Journal:  Allergy       Date:  2017-09-20       Impact factor: 13.146

7.  TRPC1 and TRPC6 channels cooperate with TRPV4 to mediate mechanical hyperalgesia and nociceptor sensitization.

Authors:  Nicole Alessandri-Haber; Olayinka A Dina; Xiaoje Chen; Jon D Levine
Journal:  J Neurosci       Date:  2009-05-13       Impact factor: 6.167

8.  C3a enhances nerve growth factor-induced NFAT activation and chemokine production in a human mast cell line, HMC-1.

Authors:  Jasimuddin Ahamed; Rampura T Venkatesha; E Berla Thangam; Hydar Ali
Journal:  J Immunol       Date:  2004-06-01       Impact factor: 5.422

Review 9.  Mast cell-orchestrated immunity to pathogens.

Authors:  Soman N Abraham; Ashley L St John
Journal:  Nat Rev Immunol       Date:  2010-06       Impact factor: 53.106

10.  MRGPR-mediated activation of local mast cells clears cutaneous bacterial infection and protects against reinfection.

Authors:  Mohammad Arifuzzaman; Yuvon R Mobley; Hae Woong Choi; Pradeep Bist; Cristina A Salinas; Zachary D Brown; Swaine L Chen; Herman F Staats; Soman N Abraham
Journal:  Sci Adv       Date:  2019-01-02       Impact factor: 14.136

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  3 in total

1.  MrgX2-SNAP-tag/cell membrane chromatography model coupled with liquid chromatography-mass spectrometry for anti-pseudo-allergic compound screening in Arnebiae Radix.

Authors:  Qianqian Jia; Jia Fu; Chunlei Gao; Hong Wang; Saisai Wang; Peida Liang; Shengli Han; Yanni Lv; Langchong He
Journal:  Anal Bioanal Chem       Date:  2022-06-13       Impact factor: 4.478

Review 2.  Mast Cell Activation Syndrome in COVID-19 and Female Reproductive Function: Theoretical Background vs. Accumulating Clinical Evidence.

Authors:  Dariusz Szukiewicz; Piotr Wojdasiewicz; Mateusz Watroba; Grzegorz Szewczyk
Journal:  J Immunol Res       Date:  2022-06-22       Impact factor: 4.493

Review 3.  Unlocking the Non-IgE-Mediated Pseudo-Allergic Reaction Puzzle with Mas-Related G-Protein Coupled Receptor Member X2 (MRGPRX2).

Authors:  Mukesh Kumar; Karthi Duraisamy; Billy-Kwok-Chong Chow
Journal:  Cells       Date:  2021-04-27       Impact factor: 6.600

  3 in total

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