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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...

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Autores principales: Zeng, Fanning, Wind, Nicholas, Mcclenaghan, Conor, Verkuyl, J. Martin, Watson, Robert P., Nash, Mark S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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