The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond

Recent research on mast cell biology has turned its focus on MRGPRX2, a new member of the Mas-related G protein-coupled subfamily of receptors (Mrgprs), originally described in nociceptive neurons of the dorsal root ganglia. MRGPRX2, a member of this group, is present not only in neurons but also in...

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Main Authors: Paola Leonor Leonor Quan, Marina Sabaté-Brescó, Yanru Guo, Margarita Martín, Gabriel Gastaminza
Format: Article
Language:English
Published: MDPI AG 2021-04-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/9/4421
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spelling doaj-c6d7055aac4948d3a570d2226caab0992021-04-23T23:03:21ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-04-01224421442110.3390/ijms22094421The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyondPaola Leonor Leonor Quan0Marina Sabaté-Brescó1Yanru Guo2Margarita Martín3Gabriel Gastaminza4Department of Allergy and Clinical Immunology, Clínica Universidad de Navarra, 31008 Pamplona, SpainDepartment of Allergy and Clinical Immunology, Clínica Universidad de Navarra, 31008 Pamplona, SpainBiochemistry Unit, Biomedicine Department, Faculty of Medicine, University of Barcelona, 08036 Barcelona, SpainBiochemistry Unit, Biomedicine Department, Faculty of Medicine, University of Barcelona, 08036 Barcelona, SpainDepartment of Allergy and Clinical Immunology, Clínica Universidad de Navarra, 31008 Pamplona, SpainRecent research on mast cell biology has turned its focus on MRGPRX2, a new member of the Mas-related G protein-coupled subfamily of receptors (Mrgprs), originally described in nociceptive neurons of the dorsal root ganglia. MRGPRX2, a member of this group, is present not only in neurons but also in mast cells (MCs), specifically, and potentially in other cells of the immune system, such as basophils and eosinophils. As emerging new functions for this receptor are studied, a variety of both natural and pharmacologic ligands are being uncovered, linked to the ability to induce receptor-mediated MC activation and degranulation. The diversity of these ligands, characterized in their human, mice, or rat homologues, seems to match that of the receptor’s interactions. Natural ligands include host defense peptides, basic molecules, and key neuropeptides such as substance P and vasointestinal peptide (known for their role in the transmission of pain and itch) as well as eosinophil granule-derived proteins. Exogenous ligands include MC secretagogues such as compound 48/80 and mastoparan, a component of bee wasp venom, and several peptidergic drugs, among which are members of the quinolone family, neuromuscular blocking agents, morphine, and vancomycin. These discoveries shed light on its capacity as a multifaceted participant in naturally occurring responses within immunity and neural stimulus perception, as in responses at the center of immune pathology. In host defense, the mice Mrgprb2 has been proven to aid mast cells in the detection of peptidic molecules from bacteria and in the release of peptides with antimicrobial activities and other immune mediators. There are several potential actions described for it in tissue homeostasis and repair. In the realm of pathologic response, there is evidence to suggest that this receptor is also involved in chronic inflammation. Furthermore, MRGPRX2 has been linked to the pathophysiology of non-IgE-mediated immediate hypersensitivity drug reactions. Different studies have shown its possible role in other allergic diseases as well, such as asthma, atopic dermatitis, contact dermatitis, and chronic spontaneous urticaria. In this review, we sought to cover its function in physiologic processes and responses, as well as in allergic and nonallergic immune disease.https://www.mdpi.com/1422-0067/22/9/4421mas-related G protein-coupled receptorsmas-related G protein-coupled receptor member X2 (MRGRPX2)mast cellshypersensitivity
collection DOAJ
language English
format Article
sources DOAJ
author Paola Leonor Leonor Quan
Marina Sabaté-Brescó
Yanru Guo
Margarita Martín
Gabriel Gastaminza
spellingShingle Paola Leonor Leonor Quan
Marina Sabaté-Brescó
Yanru Guo
Margarita Martín
Gabriel Gastaminza
The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
International Journal of Molecular Sciences
mas-related G protein-coupled receptors
mas-related G protein-coupled receptor member X2 (MRGRPX2)
mast cells
hypersensitivity
author_facet Paola Leonor Leonor Quan
Marina Sabaté-Brescó
Yanru Guo
Margarita Martín
Gabriel Gastaminza
author_sort Paola Leonor Leonor Quan
title The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
title_short The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
title_full The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
title_fullStr The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
title_full_unstemmed The Multifaceted Mas-Related G Protein-Coupled Receptor Member X2 in Allergic Diseases and beyond
title_sort multifaceted mas-related g protein-coupled receptor member x2 in allergic diseases and beyond
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-04-01
description Recent research on mast cell biology has turned its focus on MRGPRX2, a new member of the Mas-related G protein-coupled subfamily of receptors (Mrgprs), originally described in nociceptive neurons of the dorsal root ganglia. MRGPRX2, a member of this group, is present not only in neurons but also in mast cells (MCs), specifically, and potentially in other cells of the immune system, such as basophils and eosinophils. As emerging new functions for this receptor are studied, a variety of both natural and pharmacologic ligands are being uncovered, linked to the ability to induce receptor-mediated MC activation and degranulation. The diversity of these ligands, characterized in their human, mice, or rat homologues, seems to match that of the receptor’s interactions. Natural ligands include host defense peptides, basic molecules, and key neuropeptides such as substance P and vasointestinal peptide (known for their role in the transmission of pain and itch) as well as eosinophil granule-derived proteins. Exogenous ligands include MC secretagogues such as compound 48/80 and mastoparan, a component of bee wasp venom, and several peptidergic drugs, among which are members of the quinolone family, neuromuscular blocking agents, morphine, and vancomycin. These discoveries shed light on its capacity as a multifaceted participant in naturally occurring responses within immunity and neural stimulus perception, as in responses at the center of immune pathology. In host defense, the mice Mrgprb2 has been proven to aid mast cells in the detection of peptidic molecules from bacteria and in the release of peptides with antimicrobial activities and other immune mediators. There are several potential actions described for it in tissue homeostasis and repair. In the realm of pathologic response, there is evidence to suggest that this receptor is also involved in chronic inflammation. Furthermore, MRGPRX2 has been linked to the pathophysiology of non-IgE-mediated immediate hypersensitivity drug reactions. Different studies have shown its possible role in other allergic diseases as well, such as asthma, atopic dermatitis, contact dermatitis, and chronic spontaneous urticaria. In this review, we sought to cover its function in physiologic processes and responses, as well as in allergic and nonallergic immune disease.
topic mas-related G protein-coupled receptors
mas-related G protein-coupled receptor member X2 (MRGRPX2)
mast cells
hypersensitivity
url https://www.mdpi.com/1422-0067/22/9/4421
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