Cargando…

Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration

Interstitial cells of Cajal (ICC) in the myenteric plexus region (ICC-MY) of the small intestine are pacemakers that generate rhythmic depolarizations known as slow waves. Slow waves depend on activation of Ca(2+)-activated Cl(−) channels (ANO1) in ICC, propagate actively within networks of ICC-MY,...

Descripción completa

Detalles Bibliográficos
Autores principales: Drumm, Bernard T., Hennig, Grant W., Battersby, Matthew J., Cunningham, Erin K., Sung, Tae Sik, Ward, Sean M., Sanders, Kenton M., Baker, Salah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496507/
https://www.ncbi.nlm.nih.gov/pubmed/28592421
http://dx.doi.org/10.1085/jgp.201711771
_version_ 1783247994034847744
author Drumm, Bernard T.
Hennig, Grant W.
Battersby, Matthew J.
Cunningham, Erin K.
Sung, Tae Sik
Ward, Sean M.
Sanders, Kenton M.
Baker, Salah A.
author_facet Drumm, Bernard T.
Hennig, Grant W.
Battersby, Matthew J.
Cunningham, Erin K.
Sung, Tae Sik
Ward, Sean M.
Sanders, Kenton M.
Baker, Salah A.
author_sort Drumm, Bernard T.
collection PubMed
description Interstitial cells of Cajal (ICC) in the myenteric plexus region (ICC-MY) of the small intestine are pacemakers that generate rhythmic depolarizations known as slow waves. Slow waves depend on activation of Ca(2+)-activated Cl(−) channels (ANO1) in ICC, propagate actively within networks of ICC-MY, and conduct to smooth muscle cells where they generate action potentials and phasic contractions. Thus, mechanisms of Ca(2+) regulation in ICC are fundamental to the motor patterns of the bowel. Here, we characterize the nature of Ca(2+) transients in ICC-MY within intact muscles, using mice expressing a genetically encoded Ca(2+) sensor, GCaMP3, in ICC. Ca(2+) transients in ICC-MY display a complex firing pattern caused by localized Ca(2+) release events arising from multiple sites in cell somata and processes. Ca(2+) transients are clustered within the time course of slow waves but fire asynchronously during these clusters. The durations of Ca(2+) transient clusters (CTCs) correspond to slow wave durations (plateau phase). Simultaneous imaging and intracellular electrical recordings revealed that the upstroke depolarization of slow waves precedes clusters of Ca(2+) transients. Summation of CTCs results in relatively uniform Ca(2+) responses from one slow wave to another. These Ca(2+) transients are caused by Ca(2+) release from intracellular stores and depend on ryanodine receptors as well as amplification from IP(3) receptors. Reduced extracellular Ca(2+) concentrations and T-type Ca(2+) channel blockers decreased the number of firing sites and firing probability of Ca(2+) transients. In summary, the fundamental electrical events of small intestinal muscles generated by ICC-MY depend on asynchronous firing of Ca(2+) transients from multiple intracellular release sites. These events are organized into clusters by Ca(2+) influx through T-type Ca(2+) channels to sustain activation of ANO1 channels and generate the plateau phase of slow waves.
format Online
Article
Text
id pubmed-5496507
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-54965072018-01-03 Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration Drumm, Bernard T. Hennig, Grant W. Battersby, Matthew J. Cunningham, Erin K. Sung, Tae Sik Ward, Sean M. Sanders, Kenton M. Baker, Salah A. J Gen Physiol Research Articles Interstitial cells of Cajal (ICC) in the myenteric plexus region (ICC-MY) of the small intestine are pacemakers that generate rhythmic depolarizations known as slow waves. Slow waves depend on activation of Ca(2+)-activated Cl(−) channels (ANO1) in ICC, propagate actively within networks of ICC-MY, and conduct to smooth muscle cells where they generate action potentials and phasic contractions. Thus, mechanisms of Ca(2+) regulation in ICC are fundamental to the motor patterns of the bowel. Here, we characterize the nature of Ca(2+) transients in ICC-MY within intact muscles, using mice expressing a genetically encoded Ca(2+) sensor, GCaMP3, in ICC. Ca(2+) transients in ICC-MY display a complex firing pattern caused by localized Ca(2+) release events arising from multiple sites in cell somata and processes. Ca(2+) transients are clustered within the time course of slow waves but fire asynchronously during these clusters. The durations of Ca(2+) transient clusters (CTCs) correspond to slow wave durations (plateau phase). Simultaneous imaging and intracellular electrical recordings revealed that the upstroke depolarization of slow waves precedes clusters of Ca(2+) transients. Summation of CTCs results in relatively uniform Ca(2+) responses from one slow wave to another. These Ca(2+) transients are caused by Ca(2+) release from intracellular stores and depend on ryanodine receptors as well as amplification from IP(3) receptors. Reduced extracellular Ca(2+) concentrations and T-type Ca(2+) channel blockers decreased the number of firing sites and firing probability of Ca(2+) transients. In summary, the fundamental electrical events of small intestinal muscles generated by ICC-MY depend on asynchronous firing of Ca(2+) transients from multiple intracellular release sites. These events are organized into clusters by Ca(2+) influx through T-type Ca(2+) channels to sustain activation of ANO1 channels and generate the plateau phase of slow waves. The Rockefeller University Press 2017-07-03 /pmc/articles/PMC5496507/ /pubmed/28592421 http://dx.doi.org/10.1085/jgp.201711771 Text en © 2017 Drumm et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Drumm, Bernard T.
Hennig, Grant W.
Battersby, Matthew J.
Cunningham, Erin K.
Sung, Tae Sik
Ward, Sean M.
Sanders, Kenton M.
Baker, Salah A.
Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title_full Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title_fullStr Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title_full_unstemmed Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title_short Clustering of Ca(2+) transients in interstitial cells of Cajal defines slow wave duration
title_sort clustering of ca(2+) transients in interstitial cells of cajal defines slow wave duration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5496507/
https://www.ncbi.nlm.nih.gov/pubmed/28592421
http://dx.doi.org/10.1085/jgp.201711771
work_keys_str_mv AT drummbernardt clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT henniggrantw clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT battersbymatthewj clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT cunninghamerink clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT sungtaesik clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT wardseanm clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT sanderskentonm clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration
AT bakersalaha clusteringofca2transientsininterstitialcellsofcajaldefinesslowwaveduration