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Ca(2+) entry units in a superfast fish muscle

Over the past two decades, mounting evidence has demonstrated that a mechanism known as store-operated Ca(2+) entry (SOCE) plays a crucial role in sustaining skeletal muscle contractility by facilitating Ca(2+) influx from the extracellular space during sarcoplasmic reticulum (SR) Ca(2+) depletion....

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Autores principales: Kittelberger, J. Matthew, Franzini-Armstrong, Clara, Boncompagni, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649577/
https://www.ncbi.nlm.nih.gov/pubmed/36388096
http://dx.doi.org/10.3389/fphys.2022.1036594
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author Kittelberger, J. Matthew
Franzini-Armstrong, Clara
Boncompagni, Simona
author_facet Kittelberger, J. Matthew
Franzini-Armstrong, Clara
Boncompagni, Simona
author_sort Kittelberger, J. Matthew
collection PubMed
description Over the past two decades, mounting evidence has demonstrated that a mechanism known as store-operated Ca(2+) entry (SOCE) plays a crucial role in sustaining skeletal muscle contractility by facilitating Ca(2+) influx from the extracellular space during sarcoplasmic reticulum (SR) Ca(2+) depletion. We recently demonstrated that, in exercised fast-twitch muscle from mice, the incidence of Ca(2+) entry units (CEUs), newly described intracellular junctions between dead-end longitudinal transverse tubular (T-tubule) extensions and stacks of sarcoplasmic reticulum (SR) flat cisternae, strictly correlate with both the capability of fibers to maintain contractions during fatigue and enhanced Ca(2+) influx via SOCE. Here, we tested the broader relevance of this result across vertebrates by searching for the presence of CEUs in the vocal muscles of a teleost fish adapted for extended, high-frequency activity. Specifically, we examined active vs. inactive superfast sonic muscles of plainfin midshipman (Porichthys notatus). Interestingly, muscles from actively humming territorial males had a much higher incidence of CEU SR stacks relative to territorial males that were not actively vocalizing, strengthening the concept that assembly of these structures is dynamic and use-dependent, as recently described in exercised muscles from mice. Our results support the hypothesis that CEUs represent a conserved mechanism, across vertebrates, for enabling high levels of repetitive muscle activity, and also provide new insights into the adaptive mechanisms underlying the unique properties of superfast midshipman sonic muscles.
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spelling pubmed-96495772022-11-15 Ca(2+) entry units in a superfast fish muscle Kittelberger, J. Matthew Franzini-Armstrong, Clara Boncompagni, Simona Front Physiol Physiology Over the past two decades, mounting evidence has demonstrated that a mechanism known as store-operated Ca(2+) entry (SOCE) plays a crucial role in sustaining skeletal muscle contractility by facilitating Ca(2+) influx from the extracellular space during sarcoplasmic reticulum (SR) Ca(2+) depletion. We recently demonstrated that, in exercised fast-twitch muscle from mice, the incidence of Ca(2+) entry units (CEUs), newly described intracellular junctions between dead-end longitudinal transverse tubular (T-tubule) extensions and stacks of sarcoplasmic reticulum (SR) flat cisternae, strictly correlate with both the capability of fibers to maintain contractions during fatigue and enhanced Ca(2+) influx via SOCE. Here, we tested the broader relevance of this result across vertebrates by searching for the presence of CEUs in the vocal muscles of a teleost fish adapted for extended, high-frequency activity. Specifically, we examined active vs. inactive superfast sonic muscles of plainfin midshipman (Porichthys notatus). Interestingly, muscles from actively humming territorial males had a much higher incidence of CEU SR stacks relative to territorial males that were not actively vocalizing, strengthening the concept that assembly of these structures is dynamic and use-dependent, as recently described in exercised muscles from mice. Our results support the hypothesis that CEUs represent a conserved mechanism, across vertebrates, for enabling high levels of repetitive muscle activity, and also provide new insights into the adaptive mechanisms underlying the unique properties of superfast midshipman sonic muscles. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9649577/ /pubmed/36388096 http://dx.doi.org/10.3389/fphys.2022.1036594 Text en Copyright © 2022 Kittelberger, Franzini-Armstrong and Boncompagni. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Kittelberger, J. Matthew
Franzini-Armstrong, Clara
Boncompagni, Simona
Ca(2+) entry units in a superfast fish muscle
title Ca(2+) entry units in a superfast fish muscle
title_full Ca(2+) entry units in a superfast fish muscle
title_fullStr Ca(2+) entry units in a superfast fish muscle
title_full_unstemmed Ca(2+) entry units in a superfast fish muscle
title_short Ca(2+) entry units in a superfast fish muscle
title_sort ca(2+) entry units in a superfast fish muscle
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649577/
https://www.ncbi.nlm.nih.gov/pubmed/36388096
http://dx.doi.org/10.3389/fphys.2022.1036594
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