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Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon

Interstitial cells of Cajal (ICC) generate pacemaker activity responsible for phasic contractions in colonic segmentation and peristalsis. ICC along the submucosal border (ICC-SM) contribute to mixing and more complex patterns of colonic motility. We show the complex patterns of Ca(2+) signaling in...

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Autores principales: Baker, Salah A, Leigh, Wesley A, Del Valle, Guillermo, De Yturriaga, Inigo F, Ward, Sean M, Cobine, Caroline A, Drumm, Bernard T, Sanders, Kenton M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806270/
https://www.ncbi.nlm.nih.gov/pubmed/33399536
http://dx.doi.org/10.7554/eLife.64099
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author Baker, Salah A
Leigh, Wesley A
Del Valle, Guillermo
De Yturriaga, Inigo F
Ward, Sean M
Cobine, Caroline A
Drumm, Bernard T
Sanders, Kenton M
author_facet Baker, Salah A
Leigh, Wesley A
Del Valle, Guillermo
De Yturriaga, Inigo F
Ward, Sean M
Cobine, Caroline A
Drumm, Bernard T
Sanders, Kenton M
author_sort Baker, Salah A
collection PubMed
description Interstitial cells of Cajal (ICC) generate pacemaker activity responsible for phasic contractions in colonic segmentation and peristalsis. ICC along the submucosal border (ICC-SM) contribute to mixing and more complex patterns of colonic motility. We show the complex patterns of Ca(2+) signaling in ICC-SM and the relationship between ICC-SM Ca(2+) transients and activation of smooth muscle cells (SMCs) using optogenetic tools. ICC-SM displayed rhythmic firing of Ca(2+)transients ~ 15 cpm and paced adjacent SMCs. The majority of spontaneous activity occurred in regular Ca(2+) transients clusters (CTCs) that propagated through the network. CTCs were organized and dependent upon Ca(2+) entry through voltage-dependent Ca(2+) conductances, L- and T-type Ca(2+) channels. Removal of Ca(2+) from the external solution abolished CTCs. Ca(2+) release mechanisms reduced the duration and amplitude of Ca(2+) transients but did not block CTCs. These data reveal how colonic pacemaker ICC-SM exhibit complex Ca(2+-)firing patterns and drive smooth muscle activity and overall colonic contractions.
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spelling pubmed-78062702021-01-15 Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon Baker, Salah A Leigh, Wesley A Del Valle, Guillermo De Yturriaga, Inigo F Ward, Sean M Cobine, Caroline A Drumm, Bernard T Sanders, Kenton M eLife Cell Biology Interstitial cells of Cajal (ICC) generate pacemaker activity responsible for phasic contractions in colonic segmentation and peristalsis. ICC along the submucosal border (ICC-SM) contribute to mixing and more complex patterns of colonic motility. We show the complex patterns of Ca(2+) signaling in ICC-SM and the relationship between ICC-SM Ca(2+) transients and activation of smooth muscle cells (SMCs) using optogenetic tools. ICC-SM displayed rhythmic firing of Ca(2+)transients ~ 15 cpm and paced adjacent SMCs. The majority of spontaneous activity occurred in regular Ca(2+) transients clusters (CTCs) that propagated through the network. CTCs were organized and dependent upon Ca(2+) entry through voltage-dependent Ca(2+) conductances, L- and T-type Ca(2+) channels. Removal of Ca(2+) from the external solution abolished CTCs. Ca(2+) release mechanisms reduced the duration and amplitude of Ca(2+) transients but did not block CTCs. These data reveal how colonic pacemaker ICC-SM exhibit complex Ca(2+-)firing patterns and drive smooth muscle activity and overall colonic contractions. eLife Sciences Publications, Ltd 2021-01-05 /pmc/articles/PMC7806270/ /pubmed/33399536 http://dx.doi.org/10.7554/eLife.64099 Text en © 2021, Baker et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Baker, Salah A
Leigh, Wesley A
Del Valle, Guillermo
De Yturriaga, Inigo F
Ward, Sean M
Cobine, Caroline A
Drumm, Bernard T
Sanders, Kenton M
Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title_full Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title_fullStr Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title_full_unstemmed Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title_short Ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of Cajal in the murine colon
title_sort ca(2+) signaling driving pacemaker activity in submucosal interstitial cells of cajal in the murine colon
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806270/
https://www.ncbi.nlm.nih.gov/pubmed/33399536
http://dx.doi.org/10.7554/eLife.64099
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