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Calcineurin activation influences muscle phenotype in a muscle-specific fashion

BACKGROUND: The calcium activated protein phosphatase 2B, also known as calcineurin, has been implicated as a cell signaling molecule involved with transduction of physiological signals (free cytosolic Ca(2+)) into molecular signals that influence the expression of phenotype-specific genes in skelet...

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Autores principales: Talmadge, Robert J, Otis, Jeffrey S, Rittler, Matthew R, Garcia, Nicole D, Spencer, Shelly R, Lees, Simon J, Naya, Francisco J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509416/
https://www.ncbi.nlm.nih.gov/pubmed/15282035
http://dx.doi.org/10.1186/1471-2121-5-28
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author Talmadge, Robert J
Otis, Jeffrey S
Rittler, Matthew R
Garcia, Nicole D
Spencer, Shelly R
Lees, Simon J
Naya, Francisco J
author_facet Talmadge, Robert J
Otis, Jeffrey S
Rittler, Matthew R
Garcia, Nicole D
Spencer, Shelly R
Lees, Simon J
Naya, Francisco J
author_sort Talmadge, Robert J
collection PubMed
description BACKGROUND: The calcium activated protein phosphatase 2B, also known as calcineurin, has been implicated as a cell signaling molecule involved with transduction of physiological signals (free cytosolic Ca(2+)) into molecular signals that influence the expression of phenotype-specific genes in skeletal muscle. In the present study we address the role of calcineurin in mediating adaptations in myosin heavy chain (MHC) isoform expression and muscle mass using 3-month old wild-type (WT) and transgenic mice displaying high-level expression of a constitutively active form of calcineurin (MCK-CN* mice). RESULTS: Slow muscles, e.g., soleus, were significantly larger (by ~24%), whereas fast muscles, e.g., medial gastrocnemius (MG) and tibialis anterior were significantly smaller (by ~26 and ~16%, respectively) in MCK-CN* mice compared to WT. The masses of mixed phenotype muscles, such as the plantaris and the extensor digitorum longus, were not significantly changed from WT. The soleus, plantaris, MG and diaphragm displayed shifts toward slower MHC isoforms, e.g., soleus from WT mice contained ~52% MHC-I, ~39% MHC-IIa, and ~9% MHC-IIx, whereas MCK-CN* mice had ~67% MHC-I, ~26% MHC-IIa, and ~7% MHC-IIx. The specific isoforms that were either up or down-regulated were muscle-specific. For instance, the proportion of MHC-IIa was decreased in the soleus and diaphragm, but increased in the plantaris and MG of MCK-CN* mice. Also, the proportion of MHC-IIx was unchanged in the soleus, decreased in the diaphragm and increased in the plantaris and MG of MCK-CN* relative to WT mice. Fast to slow shifts in fiber type proportions were evident for the plantaris, but not the soleus. Fast, but not slow, plantaris fibers of MCK-CN* mice had higher oxidative and lower glycolytic properties than WT. CONCLUSION: These data suggest that calcineurin activation can influence muscle phenotype and that the specific influence of calcineurin activation on the phenotypic and mass characteristics of a muscle is dependent upon the original phenotypic state of the muscle.
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spelling pubmed-5094162004-08-15 Calcineurin activation influences muscle phenotype in a muscle-specific fashion Talmadge, Robert J Otis, Jeffrey S Rittler, Matthew R Garcia, Nicole D Spencer, Shelly R Lees, Simon J Naya, Francisco J BMC Cell Biol Research Article BACKGROUND: The calcium activated protein phosphatase 2B, also known as calcineurin, has been implicated as a cell signaling molecule involved with transduction of physiological signals (free cytosolic Ca(2+)) into molecular signals that influence the expression of phenotype-specific genes in skeletal muscle. In the present study we address the role of calcineurin in mediating adaptations in myosin heavy chain (MHC) isoform expression and muscle mass using 3-month old wild-type (WT) and transgenic mice displaying high-level expression of a constitutively active form of calcineurin (MCK-CN* mice). RESULTS: Slow muscles, e.g., soleus, were significantly larger (by ~24%), whereas fast muscles, e.g., medial gastrocnemius (MG) and tibialis anterior were significantly smaller (by ~26 and ~16%, respectively) in MCK-CN* mice compared to WT. The masses of mixed phenotype muscles, such as the plantaris and the extensor digitorum longus, were not significantly changed from WT. The soleus, plantaris, MG and diaphragm displayed shifts toward slower MHC isoforms, e.g., soleus from WT mice contained ~52% MHC-I, ~39% MHC-IIa, and ~9% MHC-IIx, whereas MCK-CN* mice had ~67% MHC-I, ~26% MHC-IIa, and ~7% MHC-IIx. The specific isoforms that were either up or down-regulated were muscle-specific. For instance, the proportion of MHC-IIa was decreased in the soleus and diaphragm, but increased in the plantaris and MG of MCK-CN* mice. Also, the proportion of MHC-IIx was unchanged in the soleus, decreased in the diaphragm and increased in the plantaris and MG of MCK-CN* relative to WT mice. Fast to slow shifts in fiber type proportions were evident for the plantaris, but not the soleus. Fast, but not slow, plantaris fibers of MCK-CN* mice had higher oxidative and lower glycolytic properties than WT. CONCLUSION: These data suggest that calcineurin activation can influence muscle phenotype and that the specific influence of calcineurin activation on the phenotypic and mass characteristics of a muscle is dependent upon the original phenotypic state of the muscle. BioMed Central 2004-07-28 /pmc/articles/PMC509416/ /pubmed/15282035 http://dx.doi.org/10.1186/1471-2121-5-28 Text en Copyright © 2004 Talmadge et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Talmadge, Robert J
Otis, Jeffrey S
Rittler, Matthew R
Garcia, Nicole D
Spencer, Shelly R
Lees, Simon J
Naya, Francisco J
Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title_full Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title_fullStr Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title_full_unstemmed Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title_short Calcineurin activation influences muscle phenotype in a muscle-specific fashion
title_sort calcineurin activation influences muscle phenotype in a muscle-specific fashion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509416/
https://www.ncbi.nlm.nih.gov/pubmed/15282035
http://dx.doi.org/10.1186/1471-2121-5-28
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