Cargando…

Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata

Breathing is highly sensitive to the PCO(2) of arterial blood. Although CO(2) is detected via the proxy of pH, CO(2) acting directly via Cx26 may also contribute to the regulation of breathing. Here we exploit our knowledge of the structural motif of CO(2)-binding to Cx26 to devise a dominant negati...

Descripción completa

Detalles Bibliográficos
Autores principales: van de Wiel, Joseph, Meigh, Louise, Bhandare, Amol, Cook, Jonathan, Nijjar, Sarbjit, Huckstepp, Robert, Dale, Nicholas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505967/
https://www.ncbi.nlm.nih.gov/pubmed/32958814
http://dx.doi.org/10.1038/s42003-020-01248-x
_version_ 1783584927099387904
author van de Wiel, Joseph
Meigh, Louise
Bhandare, Amol
Cook, Jonathan
Nijjar, Sarbjit
Huckstepp, Robert
Dale, Nicholas
author_facet van de Wiel, Joseph
Meigh, Louise
Bhandare, Amol
Cook, Jonathan
Nijjar, Sarbjit
Huckstepp, Robert
Dale, Nicholas
author_sort van de Wiel, Joseph
collection PubMed
description Breathing is highly sensitive to the PCO(2) of arterial blood. Although CO(2) is detected via the proxy of pH, CO(2) acting directly via Cx26 may also contribute to the regulation of breathing. Here we exploit our knowledge of the structural motif of CO(2)-binding to Cx26 to devise a dominant negative subunit (Cx26(DN)) that removes the CO(2)-sensitivity from endogenously expressed wild type Cx26. Expression of Cx26(DN) in glial cells of a circumscribed region of the mouse medulla - the caudal parapyramidal area – reduced the adaptive change in tidal volume and minute ventilation by approximately 30% at 6% inspired CO(2). As central chemosensors mediate about 70% of the total response to hypercapnia, CO(2)-sensing via Cx26 in the caudal parapyramidal area contributed about 45% of the centrally-mediated ventilatory response to CO(2). Our data unequivocally link the direct sensing of CO(2) to the chemosensory control of breathing and demonstrates that CO(2)-binding to Cx26 is a key transduction step in this fundamental process.
format Online
Article
Text
id pubmed-7505967
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-75059672020-10-05 Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata van de Wiel, Joseph Meigh, Louise Bhandare, Amol Cook, Jonathan Nijjar, Sarbjit Huckstepp, Robert Dale, Nicholas Commun Biol Article Breathing is highly sensitive to the PCO(2) of arterial blood. Although CO(2) is detected via the proxy of pH, CO(2) acting directly via Cx26 may also contribute to the regulation of breathing. Here we exploit our knowledge of the structural motif of CO(2)-binding to Cx26 to devise a dominant negative subunit (Cx26(DN)) that removes the CO(2)-sensitivity from endogenously expressed wild type Cx26. Expression of Cx26(DN) in glial cells of a circumscribed region of the mouse medulla - the caudal parapyramidal area – reduced the adaptive change in tidal volume and minute ventilation by approximately 30% at 6% inspired CO(2). As central chemosensors mediate about 70% of the total response to hypercapnia, CO(2)-sensing via Cx26 in the caudal parapyramidal area contributed about 45% of the centrally-mediated ventilatory response to CO(2). Our data unequivocally link the direct sensing of CO(2) to the chemosensory control of breathing and demonstrates that CO(2)-binding to Cx26 is a key transduction step in this fundamental process. Nature Publishing Group UK 2020-09-21 /pmc/articles/PMC7505967/ /pubmed/32958814 http://dx.doi.org/10.1038/s42003-020-01248-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
van de Wiel, Joseph
Meigh, Louise
Bhandare, Amol
Cook, Jonathan
Nijjar, Sarbjit
Huckstepp, Robert
Dale, Nicholas
Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title_full Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title_fullStr Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title_full_unstemmed Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title_short Connexin26 mediates CO(2)-dependent regulation of breathing via glial cells of the medulla oblongata
title_sort connexin26 mediates co(2)-dependent regulation of breathing via glial cells of the medulla oblongata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505967/
https://www.ncbi.nlm.nih.gov/pubmed/32958814
http://dx.doi.org/10.1038/s42003-020-01248-x
work_keys_str_mv AT vandewieljoseph connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT meighlouise connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT bhandareamol connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT cookjonathan connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT nijjarsarbjit connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT huckstepprobert connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata
AT dalenicholas connexin26mediatesco2dependentregulationofbreathingviaglialcellsofthemedullaoblongata