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Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle

Exercise promotes the formation of intracellular junctions in skeletal muscle between stacks of sarcoplasmic reticulum (SR) cisternae and extensions of transverse-tubules (TT) that increase co-localization of proteins required for store-operated Ca(2+) entry (SOCE). Here, we report that SOCE, peak C...

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Autores principales: Michelucci, Antonio, Boncompagni, Simona, Pietrangelo, Laura, García-Castañeda, Maricela, Takano, Takahiro, Malik, Sundeep, Dirksen, Robert T, Protasi, Feliciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837846/
https://www.ncbi.nlm.nih.gov/pubmed/31657717
http://dx.doi.org/10.7554/eLife.47576
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author Michelucci, Antonio
Boncompagni, Simona
Pietrangelo, Laura
García-Castañeda, Maricela
Takano, Takahiro
Malik, Sundeep
Dirksen, Robert T
Protasi, Feliciano
author_facet Michelucci, Antonio
Boncompagni, Simona
Pietrangelo, Laura
García-Castañeda, Maricela
Takano, Takahiro
Malik, Sundeep
Dirksen, Robert T
Protasi, Feliciano
author_sort Michelucci, Antonio
collection PubMed
description Exercise promotes the formation of intracellular junctions in skeletal muscle between stacks of sarcoplasmic reticulum (SR) cisternae and extensions of transverse-tubules (TT) that increase co-localization of proteins required for store-operated Ca(2+) entry (SOCE). Here, we report that SOCE, peak Ca(2+) transient amplitude and muscle force production during repetitive stimulation are increased after exercise in parallel with the time course of TT association with SR-stacks. Unexpectedly, exercise also activated constitutive Ca(2+) entry coincident with a modest decrease in total releasable Ca(2+) store content. Importantly, this decrease in releasable Ca(2+) store content observed after exercise was reversed by repetitive high-frequency stimulation, consistent with enhanced SOCE. The functional benefits of exercise on SOCE, constitutive Ca(2+) entry and muscle force production were lost in mice with muscle-specific loss of Orai1 function. These results indicate that TT association with SR-stacks enhances Orai1-dependent SOCE to optimize Ca(2+) dynamics and muscle contractile function during acute exercise.
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spelling pubmed-68378462019-11-12 Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle Michelucci, Antonio Boncompagni, Simona Pietrangelo, Laura García-Castañeda, Maricela Takano, Takahiro Malik, Sundeep Dirksen, Robert T Protasi, Feliciano eLife Cell Biology Exercise promotes the formation of intracellular junctions in skeletal muscle between stacks of sarcoplasmic reticulum (SR) cisternae and extensions of transverse-tubules (TT) that increase co-localization of proteins required for store-operated Ca(2+) entry (SOCE). Here, we report that SOCE, peak Ca(2+) transient amplitude and muscle force production during repetitive stimulation are increased after exercise in parallel with the time course of TT association with SR-stacks. Unexpectedly, exercise also activated constitutive Ca(2+) entry coincident with a modest decrease in total releasable Ca(2+) store content. Importantly, this decrease in releasable Ca(2+) store content observed after exercise was reversed by repetitive high-frequency stimulation, consistent with enhanced SOCE. The functional benefits of exercise on SOCE, constitutive Ca(2+) entry and muscle force production were lost in mice with muscle-specific loss of Orai1 function. These results indicate that TT association with SR-stacks enhances Orai1-dependent SOCE to optimize Ca(2+) dynamics and muscle contractile function during acute exercise. eLife Sciences Publications, Ltd 2019-10-28 /pmc/articles/PMC6837846/ /pubmed/31657717 http://dx.doi.org/10.7554/eLife.47576 Text en © 2019, Michelucci et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Michelucci, Antonio
Boncompagni, Simona
Pietrangelo, Laura
García-Castañeda, Maricela
Takano, Takahiro
Malik, Sundeep
Dirksen, Robert T
Protasi, Feliciano
Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title_full Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title_fullStr Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title_full_unstemmed Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title_short Transverse tubule remodeling enhances Orai1-dependent Ca(2+) entry in skeletal muscle
title_sort transverse tubule remodeling enhances orai1-dependent ca(2+) entry in skeletal muscle
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6837846/
https://www.ncbi.nlm.nih.gov/pubmed/31657717
http://dx.doi.org/10.7554/eLife.47576
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