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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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 |
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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 |
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