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Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal
Interstitial cells of Cajal (ICC) are pacemaker cells that generate electrical slow waves in gastrointestinal (GI) smooth muscles. Slow waves organize basic motor patterns, such as peristalsis and segmentation in the GI tract. Slow waves depend upon activation of Ca(2+)-activated Cl(–) channels (CaC...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093646/ https://www.ncbi.nlm.nih.gov/pubmed/32256387 http://dx.doi.org/10.3389/fphys.2020.00230 |
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author | Zheng, Haifeng Drumm, Bernard T. Zhu, Mei Hong Xie, Yeming O’Driscoll, Kate E. Baker, Salah A. Perrino, Brian A. Koh, Sang Don Sanders, Kenton M. |
author_facet | Zheng, Haifeng Drumm, Bernard T. Zhu, Mei Hong Xie, Yeming O’Driscoll, Kate E. Baker, Salah A. Perrino, Brian A. Koh, Sang Don Sanders, Kenton M. |
author_sort | Zheng, Haifeng |
collection | PubMed |
description | Interstitial cells of Cajal (ICC) are pacemaker cells that generate electrical slow waves in gastrointestinal (GI) smooth muscles. Slow waves organize basic motor patterns, such as peristalsis and segmentation in the GI tract. Slow waves depend upon activation of Ca(2+)-activated Cl(–) channels (CaCC) encoded by Ano1. Slow waves consist of an upstroke depolarization and a sustained plateau potential that is the main factor leading to excitation-contraction coupling. The plateau phase can last for seconds in some regions of the GI tract. How elevated Ca(2+) is maintained throughout the duration of slow waves, which is necessary for sustained activation of CaCC, is unknown. Modeling has suggested a role for Na(+)/Ca(2+) exchanger (NCX) in regulating CaCC currents in ICC, so we tested this idea on murine intestinal ICC. ICC of small and large intestine express NCX isoforms. NCX3 is closely associated with ANO1 in ICC, as shown by immunoprecipitation and proximity ligation assays (PLA). KB-R7943, an inhibitor of NCX, increased CaCC current in ICC, suggesting that NCX, acting in Ca(2+) exit mode, helps to regulate basal [Ca(2+)](i) in these cells. Shifting NCX into Ca(2+) entry mode by replacing extracellular Na(+) with Li(+) increased spontaneous transient inward currents (STICs), due to activation of CaCC. Stepping ICC from −80 to −40 mV activated slow wave currents that were reduced in amplitude and duration by NCX inhibitors, KB-R7943 and SN-6, and enhanced by increasing the NCX driving force. SN-6 reduced the duration of clustered Ca(2+) transients that underlie the activation of CaCC and the plateau phase of slow waves. Our results suggest that NCX participates in slow waves as modeling has predicted. Dynamic changes in membrane potential and ionic gradients during slow waves appear to flip the directionality of NCX, facilitating removal of Ca(2+) during the inter-slow wave interval and providing Ca(2+) for sustained activation of ANO1 during the slow wave plateau phase. |
format | Online Article Text |
id | pubmed-7093646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70936462020-04-01 Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal Zheng, Haifeng Drumm, Bernard T. Zhu, Mei Hong Xie, Yeming O’Driscoll, Kate E. Baker, Salah A. Perrino, Brian A. Koh, Sang Don Sanders, Kenton M. Front Physiol Physiology Interstitial cells of Cajal (ICC) are pacemaker cells that generate electrical slow waves in gastrointestinal (GI) smooth muscles. Slow waves organize basic motor patterns, such as peristalsis and segmentation in the GI tract. Slow waves depend upon activation of Ca(2+)-activated Cl(–) channels (CaCC) encoded by Ano1. Slow waves consist of an upstroke depolarization and a sustained plateau potential that is the main factor leading to excitation-contraction coupling. The plateau phase can last for seconds in some regions of the GI tract. How elevated Ca(2+) is maintained throughout the duration of slow waves, which is necessary for sustained activation of CaCC, is unknown. Modeling has suggested a role for Na(+)/Ca(2+) exchanger (NCX) in regulating CaCC currents in ICC, so we tested this idea on murine intestinal ICC. ICC of small and large intestine express NCX isoforms. NCX3 is closely associated with ANO1 in ICC, as shown by immunoprecipitation and proximity ligation assays (PLA). KB-R7943, an inhibitor of NCX, increased CaCC current in ICC, suggesting that NCX, acting in Ca(2+) exit mode, helps to regulate basal [Ca(2+)](i) in these cells. Shifting NCX into Ca(2+) entry mode by replacing extracellular Na(+) with Li(+) increased spontaneous transient inward currents (STICs), due to activation of CaCC. Stepping ICC from −80 to −40 mV activated slow wave currents that were reduced in amplitude and duration by NCX inhibitors, KB-R7943 and SN-6, and enhanced by increasing the NCX driving force. SN-6 reduced the duration of clustered Ca(2+) transients that underlie the activation of CaCC and the plateau phase of slow waves. Our results suggest that NCX participates in slow waves as modeling has predicted. Dynamic changes in membrane potential and ionic gradients during slow waves appear to flip the directionality of NCX, facilitating removal of Ca(2+) during the inter-slow wave interval and providing Ca(2+) for sustained activation of ANO1 during the slow wave plateau phase. Frontiers Media S.A. 2020-03-18 /pmc/articles/PMC7093646/ /pubmed/32256387 http://dx.doi.org/10.3389/fphys.2020.00230 Text en Copyright © 2020 Zheng, Drumm, Zhu, Xie, O’Driscoll, Baker, Perrino, Koh and Sanders. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Zheng, Haifeng Drumm, Bernard T. Zhu, Mei Hong Xie, Yeming O’Driscoll, Kate E. Baker, Salah A. Perrino, Brian A. Koh, Sang Don Sanders, Kenton M. Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title | Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title_full | Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title_fullStr | Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title_full_unstemmed | Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title_short | Na(+)/Ca(2 +) Exchange and Pacemaker Activity of Interstitial Cells of Cajal |
title_sort | na(+)/ca(2 +) exchange and pacemaker activity of interstitial cells of cajal |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7093646/ https://www.ncbi.nlm.nih.gov/pubmed/32256387 http://dx.doi.org/10.3389/fphys.2020.00230 |
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