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Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle

Glycogen is a key energy substrate in excitable tissue, including in skeletal muscle fibers where it also contributes to local energy production. Transmission electron microscopy imaging has revealed the existence of a heterogenic subcellular distribution of three distinct glycogen pools in skeletal...

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Autores principales: Nielsen, Joachim, Dubillot, Peter, Stausholm, Marie-Louise H., Ørtenblad, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270182/
https://www.ncbi.nlm.nih.gov/pubmed/35796670
http://dx.doi.org/10.1085/jgp.202113071
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author Nielsen, Joachim
Dubillot, Peter
Stausholm, Marie-Louise H.
Ørtenblad, Niels
author_facet Nielsen, Joachim
Dubillot, Peter
Stausholm, Marie-Louise H.
Ørtenblad, Niels
author_sort Nielsen, Joachim
collection PubMed
description Glycogen is a key energy substrate in excitable tissue, including in skeletal muscle fibers where it also contributes to local energy production. Transmission electron microscopy imaging has revealed the existence of a heterogenic subcellular distribution of three distinct glycogen pools in skeletal muscle, which are thought to reflect the requirements for local energy stores at the subcellular level. Here, we show that the three main energy-consuming ATPases in skeletal muscles (Ca(2+), Na(+),K(+), and myosin ATPases) utilize different local pools of glycogen. These results clearly demonstrate compartmentalized glycogen metabolism and emphasize that spatially distinct pools of glycogen particles act as energy substrate for separated energy requiring processes, suggesting a new model for understanding glycogen metabolism in working muscles, muscle fatigue, and metabolic disorders. These observations suggest that the distinct glycogen pools can regulate the functional state of mammalian muscle cells and have important implications for the understanding of how the balance between ATP utilization and ATP production is regulated at the cellular level in general and in skeletal muscle fibers in particular.
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spelling pubmed-92701822023-01-07 Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle Nielsen, Joachim Dubillot, Peter Stausholm, Marie-Louise H. Ørtenblad, Niels J Gen Physiol Article Glycogen is a key energy substrate in excitable tissue, including in skeletal muscle fibers where it also contributes to local energy production. Transmission electron microscopy imaging has revealed the existence of a heterogenic subcellular distribution of three distinct glycogen pools in skeletal muscle, which are thought to reflect the requirements for local energy stores at the subcellular level. Here, we show that the three main energy-consuming ATPases in skeletal muscles (Ca(2+), Na(+),K(+), and myosin ATPases) utilize different local pools of glycogen. These results clearly demonstrate compartmentalized glycogen metabolism and emphasize that spatially distinct pools of glycogen particles act as energy substrate for separated energy requiring processes, suggesting a new model for understanding glycogen metabolism in working muscles, muscle fatigue, and metabolic disorders. These observations suggest that the distinct glycogen pools can regulate the functional state of mammalian muscle cells and have important implications for the understanding of how the balance between ATP utilization and ATP production is regulated at the cellular level in general and in skeletal muscle fibers in particular. Rockefeller University Press 2022-07-07 /pmc/articles/PMC9270182/ /pubmed/35796670 http://dx.doi.org/10.1085/jgp.202113071 Text en © 2022 Nielsen et al. https://creativecommons.org/licenses/by-nc-sa/4.0/http://www.rupress.org/terms/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 Article
Nielsen, Joachim
Dubillot, Peter
Stausholm, Marie-Louise H.
Ørtenblad, Niels
Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title_full Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title_fullStr Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title_full_unstemmed Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title_short Specific ATPases drive compartmentalized glycogen utilization in rat skeletal muscle
title_sort specific atpases drive compartmentalized glycogen utilization in rat skeletal muscle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270182/
https://www.ncbi.nlm.nih.gov/pubmed/35796670
http://dx.doi.org/10.1085/jgp.202113071
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