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Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes

BACKGROUND: In skeletal muscle, intracellular Ca(2+) is an important regulator of contraction as well as gene expression and metabolic processes. Because of the difficulties to obtain intact human muscle fibers, human myotubes have been extensively employed for studies of Ca(2+)-dependent processes...

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Autores principales: Olsson, Karl, Cheng, Arthur J., Alam, Seher, Al-Ameri, Mamdoh, Rullman, Eric, Westerblad, Håkan, Lanner, Johanna T., Bruton, Joseph D., Gustafsson, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545874/
https://www.ncbi.nlm.nih.gov/pubmed/26301072
http://dx.doi.org/10.1186/s13395-015-0050-x
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author Olsson, Karl
Cheng, Arthur J.
Alam, Seher
Al-Ameri, Mamdoh
Rullman, Eric
Westerblad, Håkan
Lanner, Johanna T.
Bruton, Joseph D.
Gustafsson, Thomas
author_facet Olsson, Karl
Cheng, Arthur J.
Alam, Seher
Al-Ameri, Mamdoh
Rullman, Eric
Westerblad, Håkan
Lanner, Johanna T.
Bruton, Joseph D.
Gustafsson, Thomas
author_sort Olsson, Karl
collection PubMed
description BACKGROUND: In skeletal muscle, intracellular Ca(2+) is an important regulator of contraction as well as gene expression and metabolic processes. Because of the difficulties to obtain intact human muscle fibers, human myotubes have been extensively employed for studies of Ca(2+)-dependent processes in human adult muscle. Despite this, it is unknown whether the Ca(2+)-handling properties of myotubes adequately represent those of adult muscle fibers. METHODS: To enable a comparison of the Ca(2+)-handling properties of human muscle fibers and myotubes, we developed a model of dissected intact single muscle fibers obtained from human intercostal muscle biopsies. The intracellular Ca(2+)-handling of human muscle fibers was compared with that of myotubes generated by the differentiation of primary human myoblasts obtained from vastus lateralis muscle biopsies. RESULTS: The intact single muscle fibers all demonstrated strictly regulated cytosolic free [Ca(2+)] ([Ca(2+)](i)) transients and force production upon electrical stimulation. In contrast, despite a more mature Ca(2+)-handling in myotubes than in myoblasts, myotubes lacked fundamental aspects of adult Ca(2+)-handling and did not contract. These functional differences were explained by discrepancies in the quantity and localization of Ca(2+)-handling proteins, as well as ultrastructural differences between muscle fibers and myotubes. CONCLUSIONS: Intact single muscle fibers that display strictly regulated [Ca(2+)](i) transients and force production upon electrical stimulation can be obtained from human intercostal muscle biopsies. In contrast, human myotubes lack important aspects of adult Ca(2+)-handling and are thus an inappropriate model for human adult muscle when studying Ca(2+)-dependent processes, such as gene expression and metabolic processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-015-0050-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-45458742015-08-23 Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes Olsson, Karl Cheng, Arthur J. Alam, Seher Al-Ameri, Mamdoh Rullman, Eric Westerblad, Håkan Lanner, Johanna T. Bruton, Joseph D. Gustafsson, Thomas Skelet Muscle Research BACKGROUND: In skeletal muscle, intracellular Ca(2+) is an important regulator of contraction as well as gene expression and metabolic processes. Because of the difficulties to obtain intact human muscle fibers, human myotubes have been extensively employed for studies of Ca(2+)-dependent processes in human adult muscle. Despite this, it is unknown whether the Ca(2+)-handling properties of myotubes adequately represent those of adult muscle fibers. METHODS: To enable a comparison of the Ca(2+)-handling properties of human muscle fibers and myotubes, we developed a model of dissected intact single muscle fibers obtained from human intercostal muscle biopsies. The intracellular Ca(2+)-handling of human muscle fibers was compared with that of myotubes generated by the differentiation of primary human myoblasts obtained from vastus lateralis muscle biopsies. RESULTS: The intact single muscle fibers all demonstrated strictly regulated cytosolic free [Ca(2+)] ([Ca(2+)](i)) transients and force production upon electrical stimulation. In contrast, despite a more mature Ca(2+)-handling in myotubes than in myoblasts, myotubes lacked fundamental aspects of adult Ca(2+)-handling and did not contract. These functional differences were explained by discrepancies in the quantity and localization of Ca(2+)-handling proteins, as well as ultrastructural differences between muscle fibers and myotubes. CONCLUSIONS: Intact single muscle fibers that display strictly regulated [Ca(2+)](i) transients and force production upon electrical stimulation can be obtained from human intercostal muscle biopsies. In contrast, human myotubes lack important aspects of adult Ca(2+)-handling and are thus an inappropriate model for human adult muscle when studying Ca(2+)-dependent processes, such as gene expression and metabolic processes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13395-015-0050-x) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-20 /pmc/articles/PMC4545874/ /pubmed/26301072 http://dx.doi.org/10.1186/s13395-015-0050-x Text en © Olsson et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Olsson, Karl
Cheng, Arthur J.
Alam, Seher
Al-Ameri, Mamdoh
Rullman, Eric
Westerblad, Håkan
Lanner, Johanna T.
Bruton, Joseph D.
Gustafsson, Thomas
Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title_full Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title_fullStr Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title_full_unstemmed Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title_short Intracellular Ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
title_sort intracellular ca(2+)-handling differs markedly between intact human muscle fibers and myotubes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4545874/
https://www.ncbi.nlm.nih.gov/pubmed/26301072
http://dx.doi.org/10.1186/s13395-015-0050-x
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