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ASIC subunit ratio and differential surface trafficking in the brain

BACKGROUND: Acid-sensing ion channels (ASICs) are key mediators of acidosis-induced responses in neurons. However, little is known about the relative abundance of different ASIC subunits in the brain. Such data are fundamental for interpreting the relative contribution of ASIC1a homomers and 1a/2 he...

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Autores principales: Wu, Junjun, Xu, Yuanyuan, Jiang, Yu-Qing, Xu, Jiangping, Hu, Youjia, Zha, Xiang-ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706662/
https://www.ncbi.nlm.nih.gov/pubmed/26746198
http://dx.doi.org/10.1186/s13041-016-0185-7
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author Wu, Junjun
Xu, Yuanyuan
Jiang, Yu-Qing
Xu, Jiangping
Hu, Youjia
Zha, Xiang-ming
author_facet Wu, Junjun
Xu, Yuanyuan
Jiang, Yu-Qing
Xu, Jiangping
Hu, Youjia
Zha, Xiang-ming
author_sort Wu, Junjun
collection PubMed
description BACKGROUND: Acid-sensing ion channels (ASICs) are key mediators of acidosis-induced responses in neurons. However, little is known about the relative abundance of different ASIC subunits in the brain. Such data are fundamental for interpreting the relative contribution of ASIC1a homomers and 1a/2 heteromers to acid signaling, and essential for designing therapeutic interventions to target these channels. We used a simple biochemical approach and semi-quantitatively determined the molar ratio of ASIC1a and 2 subunits in mouse brain. Further, we investigated differential surface trafficking of ASIC1a, ASIC2a, and ASIC2b. RESULTS AND CONCLUSIONS: ASIC1a subunits outnumber the sum of ASIC2a and ASIC2b. There is a region-specific variation in ASIC2a and 2b expression, with cerebellum and striatum expressing predominantly 2b and 2a, respectively. Further, we performed surface biotinylation and found that surface ASIC1a and ASIC2a ratio correlates with their total expression. In contrast, ASIC2b exhibits little surface presence in the brain. This result is consistent with increased co-localization of ASIC2b with an ER marker in 3T3 cells. Our data are the first semi-quantitative determination of relative subunit ratio of various ASICs in the brain. The differential surface trafficking of ASICs suggests that the main functional ASICs in the brain are ASIC1a homomers and 1a/2a heteromers. This finding provides important insights into the relative contribution of various ASIC complexes to acid signaling in neurons.
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spelling pubmed-47066622016-01-10 ASIC subunit ratio and differential surface trafficking in the brain Wu, Junjun Xu, Yuanyuan Jiang, Yu-Qing Xu, Jiangping Hu, Youjia Zha, Xiang-ming Mol Brain Research BACKGROUND: Acid-sensing ion channels (ASICs) are key mediators of acidosis-induced responses in neurons. However, little is known about the relative abundance of different ASIC subunits in the brain. Such data are fundamental for interpreting the relative contribution of ASIC1a homomers and 1a/2 heteromers to acid signaling, and essential for designing therapeutic interventions to target these channels. We used a simple biochemical approach and semi-quantitatively determined the molar ratio of ASIC1a and 2 subunits in mouse brain. Further, we investigated differential surface trafficking of ASIC1a, ASIC2a, and ASIC2b. RESULTS AND CONCLUSIONS: ASIC1a subunits outnumber the sum of ASIC2a and ASIC2b. There is a region-specific variation in ASIC2a and 2b expression, with cerebellum and striatum expressing predominantly 2b and 2a, respectively. Further, we performed surface biotinylation and found that surface ASIC1a and ASIC2a ratio correlates with their total expression. In contrast, ASIC2b exhibits little surface presence in the brain. This result is consistent with increased co-localization of ASIC2b with an ER marker in 3T3 cells. Our data are the first semi-quantitative determination of relative subunit ratio of various ASICs in the brain. The differential surface trafficking of ASICs suggests that the main functional ASICs in the brain are ASIC1a homomers and 1a/2a heteromers. This finding provides important insights into the relative contribution of various ASIC complexes to acid signaling in neurons. BioMed Central 2016-01-08 /pmc/articles/PMC4706662/ /pubmed/26746198 http://dx.doi.org/10.1186/s13041-016-0185-7 Text en © Wu et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wu, Junjun
Xu, Yuanyuan
Jiang, Yu-Qing
Xu, Jiangping
Hu, Youjia
Zha, Xiang-ming
ASIC subunit ratio and differential surface trafficking in the brain
title ASIC subunit ratio and differential surface trafficking in the brain
title_full ASIC subunit ratio and differential surface trafficking in the brain
title_fullStr ASIC subunit ratio and differential surface trafficking in the brain
title_full_unstemmed ASIC subunit ratio and differential surface trafficking in the brain
title_short ASIC subunit ratio and differential surface trafficking in the brain
title_sort asic subunit ratio and differential surface trafficking in the brain
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4706662/
https://www.ncbi.nlm.nih.gov/pubmed/26746198
http://dx.doi.org/10.1186/s13041-016-0185-7
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