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Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor
The main inhibitory neurotransmitter, GABA, acts on both ligand-gated and G protein-coupled receptors, the GABA(A/C) and GABA(B) receptors, respectively. The later play important roles in modulating many synapses, both at the pre- and post-synaptic levels, and are then still considered as interestin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920572/ https://www.ncbi.nlm.nih.gov/pubmed/24575041 http://dx.doi.org/10.3389/fphar.2014.00012 |
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author | Xu, Chanjuan Zhang, Wenhua Rondard, Philippe Pin, Jean-Philippe Liu, Jianfeng |
author_facet | Xu, Chanjuan Zhang, Wenhua Rondard, Philippe Pin, Jean-Philippe Liu, Jianfeng |
author_sort | Xu, Chanjuan |
collection | PubMed |
description | The main inhibitory neurotransmitter, GABA, acts on both ligand-gated and G protein-coupled receptors, the GABA(A/C) and GABA(B) receptors, respectively. The later play important roles in modulating many synapses, both at the pre- and post-synaptic levels, and are then still considered as interesting targets to treat a number of brain diseases, including addiction. For many years, several subtypes of GABA(B) receptors were expected, but cloning revealed only two genes that work in concert to generate a single type of GABA(B) receptor composed of two subunits. Here we will show that the signaling complexity of this unit receptor type can be largely increased through various ways, including receptor stoichiometry, subunit isoforms, cell-surface expression and localization, crosstalk with other receptors, or interacting proteins. These recent data revealed how complexity of a receptor unit can be increased, observation that certainly are not unique to the GABA(B) receptor. |
format | Online Article Text |
id | pubmed-3920572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39205722014-02-26 Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor Xu, Chanjuan Zhang, Wenhua Rondard, Philippe Pin, Jean-Philippe Liu, Jianfeng Front Pharmacol Pharmacology The main inhibitory neurotransmitter, GABA, acts on both ligand-gated and G protein-coupled receptors, the GABA(A/C) and GABA(B) receptors, respectively. The later play important roles in modulating many synapses, both at the pre- and post-synaptic levels, and are then still considered as interesting targets to treat a number of brain diseases, including addiction. For many years, several subtypes of GABA(B) receptors were expected, but cloning revealed only two genes that work in concert to generate a single type of GABA(B) receptor composed of two subunits. Here we will show that the signaling complexity of this unit receptor type can be largely increased through various ways, including receptor stoichiometry, subunit isoforms, cell-surface expression and localization, crosstalk with other receptors, or interacting proteins. These recent data revealed how complexity of a receptor unit can be increased, observation that certainly are not unique to the GABA(B) receptor. Frontiers Media S.A. 2014-02-11 /pmc/articles/PMC3920572/ /pubmed/24575041 http://dx.doi.org/10.3389/fphar.2014.00012 Text en Copyright © 2014 Xu, Zhang, Rondard, Pin and Liu. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Xu, Chanjuan Zhang, Wenhua Rondard, Philippe Pin, Jean-Philippe Liu, Jianfeng Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title | Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title_full | Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title_fullStr | Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title_full_unstemmed | Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title_short | Complex GABA(B) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
title_sort | complex gaba(b) receptor complexes: how to generate multiple functionally distinct units from a single receptor |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920572/ https://www.ncbi.nlm.nih.gov/pubmed/24575041 http://dx.doi.org/10.3389/fphar.2014.00012 |
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