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Acid-Sensing Ion Channel 2: Function and Modulation

Acid-sensing ion channels (ASICs) have an important influence on human physiology and pathology. They are members of the degenerin/epithelial sodium channel family. Four genes encode at least six subunits, which combine to form a variety of homotrimers and heterotrimers. Of these, ASIC1a homotrimers...

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Autores principales: Sivils, Andy, Yang, Felix, Wang, John Q., Chu, Xiang-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880099/
https://www.ncbi.nlm.nih.gov/pubmed/35207035
http://dx.doi.org/10.3390/membranes12020113
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author Sivils, Andy
Yang, Felix
Wang, John Q.
Chu, Xiang-Ping
author_facet Sivils, Andy
Yang, Felix
Wang, John Q.
Chu, Xiang-Ping
author_sort Sivils, Andy
collection PubMed
description Acid-sensing ion channels (ASICs) have an important influence on human physiology and pathology. They are members of the degenerin/epithelial sodium channel family. Four genes encode at least six subunits, which combine to form a variety of homotrimers and heterotrimers. Of these, ASIC1a homotrimers and ASIC1a/2 heterotrimers are most widely expressed in the central nervous system (CNS). Investigations into the function of ASIC1a in the CNS have revealed a wealth of information, culminating in multiple contemporary reviews. The lesser-studied ASIC2 subunits are in need of examination. This review will focus on ASIC2 in health and disease, with discussions of its role in modulating ASIC function, synaptic targeting, cardiovascular responses, and pharmacology, while exploring evidence of its influence in pathologies such as ischemic brain injury, multiple sclerosis, epilepsy, migraines, drug addiction, etc. This information substantiates the ASIC2 protein as a potential therapeutic target for various neurological, psychological, and cerebrovascular diseases.
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spelling pubmed-88800992022-02-26 Acid-Sensing Ion Channel 2: Function and Modulation Sivils, Andy Yang, Felix Wang, John Q. Chu, Xiang-Ping Membranes (Basel) Review Acid-sensing ion channels (ASICs) have an important influence on human physiology and pathology. They are members of the degenerin/epithelial sodium channel family. Four genes encode at least six subunits, which combine to form a variety of homotrimers and heterotrimers. Of these, ASIC1a homotrimers and ASIC1a/2 heterotrimers are most widely expressed in the central nervous system (CNS). Investigations into the function of ASIC1a in the CNS have revealed a wealth of information, culminating in multiple contemporary reviews. The lesser-studied ASIC2 subunits are in need of examination. This review will focus on ASIC2 in health and disease, with discussions of its role in modulating ASIC function, synaptic targeting, cardiovascular responses, and pharmacology, while exploring evidence of its influence in pathologies such as ischemic brain injury, multiple sclerosis, epilepsy, migraines, drug addiction, etc. This information substantiates the ASIC2 protein as a potential therapeutic target for various neurological, psychological, and cerebrovascular diseases. MDPI 2022-01-19 /pmc/articles/PMC8880099/ /pubmed/35207035 http://dx.doi.org/10.3390/membranes12020113 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sivils, Andy
Yang, Felix
Wang, John Q.
Chu, Xiang-Ping
Acid-Sensing Ion Channel 2: Function and Modulation
title Acid-Sensing Ion Channel 2: Function and Modulation
title_full Acid-Sensing Ion Channel 2: Function and Modulation
title_fullStr Acid-Sensing Ion Channel 2: Function and Modulation
title_full_unstemmed Acid-Sensing Ion Channel 2: Function and Modulation
title_short Acid-Sensing Ion Channel 2: Function and Modulation
title_sort acid-sensing ion channel 2: function and modulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880099/
https://www.ncbi.nlm.nih.gov/pubmed/35207035
http://dx.doi.org/10.3390/membranes12020113
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