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Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon
The longitudinal muscle layer in gut is the functional opponent to the circular muscle layer during peristalsis. Differences in innervation of the layers allow for the contraction of one layer concurrently with the relaxation of the other, enabling the passage of gut contents in a controlled fashion...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japan Society of Smooth Muscle Research
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862207/ https://www.ncbi.nlm.nih.gov/pubmed/25891767 http://dx.doi.org/10.1540/jsmr.50.103 |
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author | Anderson, Charles D. Kendig, Derek M. Al-qudah, Mohammad Mahavadi, Sunila Murthy, Karnam S. Grider, John R. |
author_facet | Anderson, Charles D. Kendig, Derek M. Al-qudah, Mohammad Mahavadi, Sunila Murthy, Karnam S. Grider, John R. |
author_sort | Anderson, Charles D. |
collection | PubMed |
description | The longitudinal muscle layer in gut is the functional opponent to the circular muscle layer during peristalsis. Differences in innervation of the layers allow for the contraction of one layer concurrently with the relaxation of the other, enabling the passage of gut contents in a controlled fashion. Differences in development have given the cells of the two layers differences in receptor populations, membrane lipid handling, and calcium handling profiles/behaviors. The contractile activity of the longitudinal muscle is largely mediated by cholinergic neural input from myenteric plexus. Activation of muscarinic receptors leads to rapid activation of several kinases including MLC kinase, ERK1/2, CaMKII and Rho kinase. Phosphorylation of myosin light chain (MLC(20)) by MLC kinase (MLCK) is a prerequisite for contraction in both circular and longitudinal muscle cells. In rat colonic longitudinal muscle strips, we measured muscarinic receptor-mediated contraction following incubation with kinase inhibitors. Basal tension was differentially regulated by Rho kinase, ERK1/2, CaMKII and CaMKK. Selective inhibitors of Rho kinase, ERK1/2, CaMKK/AMPK, and CaMKII each reduced carbachol-induced contraction in the innervated muscle strips. These inhibitors had no direct effect on MLCK activity. Thus unlike previously reported for isolated muscle cells where CaMKII and ERK1/2 are not involved in contraction, we conclude that the regulation of carbachol-induced contraction in innervated longitudinal muscle strips involves the interplay of Rho kinase, ERK1/2, CaMKK/AMPK, and CAMKII. |
format | Online Article Text |
id | pubmed-4862207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Japan Society of Smooth Muscle Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-48622072016-05-10 Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon Anderson, Charles D. Kendig, Derek M. Al-qudah, Mohammad Mahavadi, Sunila Murthy, Karnam S. Grider, John R. J Smooth Muscle Res Original The longitudinal muscle layer in gut is the functional opponent to the circular muscle layer during peristalsis. Differences in innervation of the layers allow for the contraction of one layer concurrently with the relaxation of the other, enabling the passage of gut contents in a controlled fashion. Differences in development have given the cells of the two layers differences in receptor populations, membrane lipid handling, and calcium handling profiles/behaviors. The contractile activity of the longitudinal muscle is largely mediated by cholinergic neural input from myenteric plexus. Activation of muscarinic receptors leads to rapid activation of several kinases including MLC kinase, ERK1/2, CaMKII and Rho kinase. Phosphorylation of myosin light chain (MLC(20)) by MLC kinase (MLCK) is a prerequisite for contraction in both circular and longitudinal muscle cells. In rat colonic longitudinal muscle strips, we measured muscarinic receptor-mediated contraction following incubation with kinase inhibitors. Basal tension was differentially regulated by Rho kinase, ERK1/2, CaMKII and CaMKK. Selective inhibitors of Rho kinase, ERK1/2, CaMKK/AMPK, and CaMKII each reduced carbachol-induced contraction in the innervated muscle strips. These inhibitors had no direct effect on MLCK activity. Thus unlike previously reported for isolated muscle cells where CaMKII and ERK1/2 are not involved in contraction, we conclude that the regulation of carbachol-induced contraction in innervated longitudinal muscle strips involves the interplay of Rho kinase, ERK1/2, CaMKK/AMPK, and CAMKII. Japan Society of Smooth Muscle Research 2015-04-17 2014 /pmc/articles/PMC4862207/ /pubmed/25891767 http://dx.doi.org/10.1540/jsmr.50.103 Text en ©2014 The Japan Society of Smooth Muscle Research http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Anderson, Charles D. Kendig, Derek M. Al-qudah, Mohammad Mahavadi, Sunila Murthy, Karnam S. Grider, John R. Role of various kinases in muscarinic M3 receptor-mediated contraction of longitudinal muscle of rat colon |
title | Role of various kinases in muscarinic M3 receptor-mediated contraction of
longitudinal muscle of rat colon |
title_full | Role of various kinases in muscarinic M3 receptor-mediated contraction of
longitudinal muscle of rat colon |
title_fullStr | Role of various kinases in muscarinic M3 receptor-mediated contraction of
longitudinal muscle of rat colon |
title_full_unstemmed | Role of various kinases in muscarinic M3 receptor-mediated contraction of
longitudinal muscle of rat colon |
title_short | Role of various kinases in muscarinic M3 receptor-mediated contraction of
longitudinal muscle of rat colon |
title_sort | role of various kinases in muscarinic m3 receptor-mediated contraction of
longitudinal muscle of rat colon |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862207/ https://www.ncbi.nlm.nih.gov/pubmed/25891767 http://dx.doi.org/10.1540/jsmr.50.103 |
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