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GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells
GPR39 is a GPCR implicated as a regulator of gastrointestinal motility, although the mechanism remains elusive. Here, we report that GPR39 is expressed by a specific cell population cultured from mouse small intestine muscle layers, which was subsequently identified as fibroblast-like cells (FLCs) t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485058/ https://www.ncbi.nlm.nih.gov/pubmed/23133519 http://dx.doi.org/10.1371/journal.pone.0047686 |
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author | Zeng, Fanning Wind, Nicholas Mcclenaghan, Conor Verkuyl, J. Martin Watson, Robert P. Nash, Mark S. |
author_facet | Zeng, Fanning Wind, Nicholas Mcclenaghan, Conor Verkuyl, J. Martin Watson, Robert P. Nash, Mark S. |
author_sort | Zeng, Fanning |
collection | PubMed |
description | GPR39 is a GPCR implicated as a regulator of gastrointestinal motility, although the mechanism remains elusive. Here, we report that GPR39 is expressed by a specific cell population cultured from mouse small intestine muscle layers, which was subsequently identified as fibroblast-like cells (FLCs) that have recently been shown to modulate gut motility. Application of the GPR39 agonist, Zn(2+), induced large currents and membrane depolarization in FLCs cultured from wild-type mice, but not Gpr39 (−/−) mice. This Zn(2+)-induced current could be suppressed by application of a TMEM16A antagonist, CaCC(inh)-A01, or by silencing Tmem16a expression. These data suggest that GPR39 might modulate gut motility via regulating TMEM16A function in FLCs. |
format | Online Article Text |
id | pubmed-3485058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34850582012-11-06 GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells Zeng, Fanning Wind, Nicholas Mcclenaghan, Conor Verkuyl, J. Martin Watson, Robert P. Nash, Mark S. PLoS One Research Article GPR39 is a GPCR implicated as a regulator of gastrointestinal motility, although the mechanism remains elusive. Here, we report that GPR39 is expressed by a specific cell population cultured from mouse small intestine muscle layers, which was subsequently identified as fibroblast-like cells (FLCs) that have recently been shown to modulate gut motility. Application of the GPR39 agonist, Zn(2+), induced large currents and membrane depolarization in FLCs cultured from wild-type mice, but not Gpr39 (−/−) mice. This Zn(2+)-induced current could be suppressed by application of a TMEM16A antagonist, CaCC(inh)-A01, or by silencing Tmem16a expression. These data suggest that GPR39 might modulate gut motility via regulating TMEM16A function in FLCs. Public Library of Science 2012-10-25 /pmc/articles/PMC3485058/ /pubmed/23133519 http://dx.doi.org/10.1371/journal.pone.0047686 Text en © 2012 Zeng et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zeng, Fanning Wind, Nicholas Mcclenaghan, Conor Verkuyl, J. Martin Watson, Robert P. Nash, Mark S. GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title | GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title_full | GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title_fullStr | GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title_full_unstemmed | GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title_short | GPR39 Is Coupled to TMEM16A in Intestinal Fibroblast-Like Cells |
title_sort | gpr39 is coupled to tmem16a in intestinal fibroblast-like cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485058/ https://www.ncbi.nlm.nih.gov/pubmed/23133519 http://dx.doi.org/10.1371/journal.pone.0047686 |
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