The Origin, Expression, Function and Future Research Focus of a G Protein-coupled Receptor, Mas-related Gene X2 (MrgX2)
- PMID: 26106044
- DOI: 10.1016/j.proghi.2015.06.001
The Origin, Expression, Function and Future Research Focus of a G Protein-coupled Receptor, Mas-related Gene X2 (MrgX2)
Abstract
Mas-related genes (Mrgs) belong to a large family of G protein-coupled receptor genes found in rodents. Human MRGX proteins are G protein-coupled 7-transmembrane proteins sharing 41-52% amino acid identity with each other, but have no orthologs in rodents. MrgX2 is a member of the MrgX family. MRGX2 is expressed in the small neurons of sensory ganglia and mast cells. It can interact with a series of factors and genes such as the peptides substance P, vasoactive intestinal peptide, cortistatin (CST), proadrenomedullin N-terminal peptide (PAMP), LL-37, PMX-53 and β-defensins. MRGX2 is related to nociception, adrenal gland secretion and mast cell degranulation. Recent research on MrgX2 provides insights into its role in nociception and anti-microbial activities. This article reviewed the origin, expression and function of MrgX2, and discussed possible future research focus.
Keywords: Mas-related gene X2 (MrgX2); dorsal root ganglion (DRG); immunity.; mast cell; nociception.
Copyright © 2015 The Authors. Published by Elsevier GmbH.. All rights reserved.
Similar articles
-
Mas-related gene X2 (MrgX2) is a novel G protein-coupled receptor for the antimicrobial peptide LL-37 in human mast cells: resistance to receptor phosphorylation, desensitization, and internalization.J Biol Chem. 2011 Dec 30;286(52):44739-49. doi: 10.1074/jbc.M111.277152. Epub 2011 Nov 8. J Biol Chem. 2011. PMID: 22069323 Free PMC article.
-
Expression of Mas-related gene X2 on mast cells is upregulated in the skin of patients with severe chronic urticaria.J Allergy Clin Immunol. 2014 Sep;134(3):622-633.e9. doi: 10.1016/j.jaci.2014.05.004. Epub 2014 Jun 19. J Allergy Clin Immunol. 2014. PMID: 24954276
-
G protein coupled receptor specificity for C3a and compound 48/80-induced degranulation in human mast cells: roles of Mas-related genes MrgX1 and MrgX2.Eur J Pharmacol. 2011 Oct 1;668(1-2):299-304. doi: 10.1016/j.ejphar.2011.06.027. Epub 2011 Jul 3. Eur J Pharmacol. 2011. PMID: 21741965 Free PMC article.
-
The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and Beyond.Int J Mol Sci. 2021 Apr 23;22(9):4421. doi: 10.3390/ijms22094421. Int J Mol Sci. 2021. PMID: 33922606 Free PMC article. Review.
-
Emerging Roles for MAS-Related G Protein-Coupled Receptor-X2 in Host Defense Peptide, Opioid, and Neuropeptide-Mediated Inflammatory Reactions.Adv Immunol. 2017;136:123-162. doi: 10.1016/bs.ai.2017.06.002. Epub 2017 Jul 24. Adv Immunol. 2017. PMID: 28950944 Review.
Cited by
-
Evolutionary scenarios for the specific recognition of nonhomologous endogenous peptides by G protein-coupled receptor paralogs.J Biol Chem. 2025 Feb;301(2):108125. doi: 10.1016/j.jbc.2024.108125. Epub 2024 Dec 25. J Biol Chem. 2025. PMID: 39725036 Free PMC article.
-
Involvement of Neuro-Immune Interactions in Pruritus With Special Focus on Receptor Expressions.Front Med (Lausanne). 2021 Feb 18;8:627985. doi: 10.3389/fmed.2021.627985. eCollection 2021. Front Med (Lausanne). 2021. PMID: 33681256 Free PMC article. Review.
-
MrgprF acts as a tumor suppressor in cutaneous melanoma by restraining PI3K/Akt signaling.Signal Transduct Target Ther. 2022 May 4;7(1):147. doi: 10.1038/s41392-022-00945-9. Signal Transduct Target Ther. 2022. PMID: 35504869 Free PMC article.
-
Unlocking the Non-IgE-Mediated Pseudo-Allergic Reaction Puzzle with Mas-Related G-Protein Coupled Receptor Member X2 (MRGPRX2).Cells. 2021 Apr 27;10(5):1033. doi: 10.3390/cells10051033. Cells. 2021. PMID: 33925682 Free PMC article. Review.
-
Ligands and Signaling of Mas-Related G Protein-Coupled Receptor-X2 in Mast Cell Activation.Rev Physiol Biochem Pharmacol. 2021;179:139-188. doi: 10.1007/112_2020_53. Rev Physiol Biochem Pharmacol. 2021. PMID: 33479839
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical