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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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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. |
format | Online Article Text |
id | pubmed-6837846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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