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Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia

Transient receptor potential vanilloid 4 (TRPV4) is a polymodal Ca(2+)-permeable channel involved in various hypoxia-sensitive pathophysiological phenomena. Different tools are available to study channel activity, requiring cells to be cultured at specific optimal densities. In the present study, we...

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Autores principales: Barbeau, Solène, Joushomme, Alexandre, Chappe, Yann, Cardouat, Guillaume, Baudrimont, Isabelle, Freund-Michel, Véronique, Guibert, Christelle, Marthan, Roger, Berger, Patrick, Vacher, Pierre, Percherancier, Yann, Quignard, Jean-François, Ducret, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313184/
https://www.ncbi.nlm.nih.gov/pubmed/35883510
http://dx.doi.org/10.3390/biom12070954
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author Barbeau, Solène
Joushomme, Alexandre
Chappe, Yann
Cardouat, Guillaume
Baudrimont, Isabelle
Freund-Michel, Véronique
Guibert, Christelle
Marthan, Roger
Berger, Patrick
Vacher, Pierre
Percherancier, Yann
Quignard, Jean-François
Ducret, Thomas
author_facet Barbeau, Solène
Joushomme, Alexandre
Chappe, Yann
Cardouat, Guillaume
Baudrimont, Isabelle
Freund-Michel, Véronique
Guibert, Christelle
Marthan, Roger
Berger, Patrick
Vacher, Pierre
Percherancier, Yann
Quignard, Jean-François
Ducret, Thomas
author_sort Barbeau, Solène
collection PubMed
description Transient receptor potential vanilloid 4 (TRPV4) is a polymodal Ca(2+)-permeable channel involved in various hypoxia-sensitive pathophysiological phenomena. Different tools are available to study channel activity, requiring cells to be cultured at specific optimal densities. In the present study, we examined if cell density may influence the effect of hypoxia on TRPV4 activity. Transiently TRPV4-transfected HEK293T cells were seeded at low or high densities corresponding to non-confluent or confluent cells, respectively, on the day of experiments, and cultured under in vitro normoxia or hypoxia. TRPV4-mediated cytosolic Ca(2+) responses, single-channel currents, and Ca(2+) influx through the channel were measured using Ca(2+) imaging/microspectrofluorimetric assay, patch-clamp, and Bioluminescence Resonance Energy Transfer (BRET), respectively. TRPV4 plasma membrane translocation was studied using confocal microscopy, biotinylation of cell surface proteins, and BRET. Our results show that hypoxia exposure has a differential effect on TRPV4 activation depending on cell confluence. At low confluence levels, TRPV4 response is increased in hypoxia, whereas at high confluence levels, TRPV4 response is strongly inhibited, due to channel internalization. Thus, cell density appears to be a crucial parameter for TRPV4 channel activity.
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spelling pubmed-93131842022-07-26 Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia Barbeau, Solène Joushomme, Alexandre Chappe, Yann Cardouat, Guillaume Baudrimont, Isabelle Freund-Michel, Véronique Guibert, Christelle Marthan, Roger Berger, Patrick Vacher, Pierre Percherancier, Yann Quignard, Jean-François Ducret, Thomas Biomolecules Article Transient receptor potential vanilloid 4 (TRPV4) is a polymodal Ca(2+)-permeable channel involved in various hypoxia-sensitive pathophysiological phenomena. Different tools are available to study channel activity, requiring cells to be cultured at specific optimal densities. In the present study, we examined if cell density may influence the effect of hypoxia on TRPV4 activity. Transiently TRPV4-transfected HEK293T cells were seeded at low or high densities corresponding to non-confluent or confluent cells, respectively, on the day of experiments, and cultured under in vitro normoxia or hypoxia. TRPV4-mediated cytosolic Ca(2+) responses, single-channel currents, and Ca(2+) influx through the channel were measured using Ca(2+) imaging/microspectrofluorimetric assay, patch-clamp, and Bioluminescence Resonance Energy Transfer (BRET), respectively. TRPV4 plasma membrane translocation was studied using confocal microscopy, biotinylation of cell surface proteins, and BRET. Our results show that hypoxia exposure has a differential effect on TRPV4 activation depending on cell confluence. At low confluence levels, TRPV4 response is increased in hypoxia, whereas at high confluence levels, TRPV4 response is strongly inhibited, due to channel internalization. Thus, cell density appears to be a crucial parameter for TRPV4 channel activity. MDPI 2022-07-07 /pmc/articles/PMC9313184/ /pubmed/35883510 http://dx.doi.org/10.3390/biom12070954 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 Article
Barbeau, Solène
Joushomme, Alexandre
Chappe, Yann
Cardouat, Guillaume
Baudrimont, Isabelle
Freund-Michel, Véronique
Guibert, Christelle
Marthan, Roger
Berger, Patrick
Vacher, Pierre
Percherancier, Yann
Quignard, Jean-François
Ducret, Thomas
Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title_full Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title_fullStr Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title_full_unstemmed Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title_short Cell Confluence Modulates TRPV4 Channel Activity in Response to Hypoxia
title_sort cell confluence modulates trpv4 channel activity in response to hypoxia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313184/
https://www.ncbi.nlm.nih.gov/pubmed/35883510
http://dx.doi.org/10.3390/biom12070954
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