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Structural variability of dyads relates to calcium release in rat ventricular myocytes

Cardiac excitation-contraction coupling relies on dyads, the intracellular calcium synapses of cardiac myocytes, where the plasma membrane contacts sarcoplasmic reticulum and where electrical excitation triggers calcium release. The morphology of dyads and dynamics of local calcium release vary subs...

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Autores principales: Novotová, Marta, Zahradníková, Alexandra, Nichtová, Zuzana, Kováč, Radoslav, Kráľová, Eva, Stankovičová, Tatiana, Zahradník, Ivan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229197/
https://www.ncbi.nlm.nih.gov/pubmed/32415205
http://dx.doi.org/10.1038/s41598-020-64840-5
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author Novotová, Marta
Zahradníková, Alexandra
Nichtová, Zuzana
Kováč, Radoslav
Kráľová, Eva
Stankovičová, Tatiana
Zahradníková, Alexandra
Zahradník, Ivan
author_facet Novotová, Marta
Zahradníková, Alexandra
Nichtová, Zuzana
Kováč, Radoslav
Kráľová, Eva
Stankovičová, Tatiana
Zahradníková, Alexandra
Zahradník, Ivan
author_sort Novotová, Marta
collection PubMed
description Cardiac excitation-contraction coupling relies on dyads, the intracellular calcium synapses of cardiac myocytes, where the plasma membrane contacts sarcoplasmic reticulum and where electrical excitation triggers calcium release. The morphology of dyads and dynamics of local calcium release vary substantially. To better understand the correspondence between the structure and the functionality of dyads, we estimated incidences of structurally different dyads and of kinetically different calcium release sites and tested their responsiveness to experimental myocardial injury in left ventricular myocytes of rats. According to the structure of dyads estimated in random electron microscopic images of myocardial tissue, the dyads were sorted into ‘compact’ or ‘loose’ types. The calcium release fluxes, triggered at local calcium release sites in patch-clamped ventricular myocytes and recorded by laser scanning confocal fluorescence microscopy, were decomposed into ‘early’ and ‘late’ components. ANOVA tests revealed very high correlation between the relative amplitudes of early and late calcium release flux components and the relative occurrences of compact and loose dyads in the control and in the injured myocardium. This finding ascertained the relationship between the structure of dyads and the functionality of calcium release sites and the responsiveness of calcium release sites to physical load in cardiac myocytes.
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spelling pubmed-72291972020-05-26 Structural variability of dyads relates to calcium release in rat ventricular myocytes Novotová, Marta Zahradníková, Alexandra Nichtová, Zuzana Kováč, Radoslav Kráľová, Eva Stankovičová, Tatiana Zahradníková, Alexandra Zahradník, Ivan Sci Rep Article Cardiac excitation-contraction coupling relies on dyads, the intracellular calcium synapses of cardiac myocytes, where the plasma membrane contacts sarcoplasmic reticulum and where electrical excitation triggers calcium release. The morphology of dyads and dynamics of local calcium release vary substantially. To better understand the correspondence between the structure and the functionality of dyads, we estimated incidences of structurally different dyads and of kinetically different calcium release sites and tested their responsiveness to experimental myocardial injury in left ventricular myocytes of rats. According to the structure of dyads estimated in random electron microscopic images of myocardial tissue, the dyads were sorted into ‘compact’ or ‘loose’ types. The calcium release fluxes, triggered at local calcium release sites in patch-clamped ventricular myocytes and recorded by laser scanning confocal fluorescence microscopy, were decomposed into ‘early’ and ‘late’ components. ANOVA tests revealed very high correlation between the relative amplitudes of early and late calcium release flux components and the relative occurrences of compact and loose dyads in the control and in the injured myocardium. This finding ascertained the relationship between the structure of dyads and the functionality of calcium release sites and the responsiveness of calcium release sites to physical load in cardiac myocytes. Nature Publishing Group UK 2020-05-15 /pmc/articles/PMC7229197/ /pubmed/32415205 http://dx.doi.org/10.1038/s41598-020-64840-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Novotová, Marta
Zahradníková, Alexandra
Nichtová, Zuzana
Kováč, Radoslav
Kráľová, Eva
Stankovičová, Tatiana
Zahradníková, Alexandra
Zahradník, Ivan
Structural variability of dyads relates to calcium release in rat ventricular myocytes
title Structural variability of dyads relates to calcium release in rat ventricular myocytes
title_full Structural variability of dyads relates to calcium release in rat ventricular myocytes
title_fullStr Structural variability of dyads relates to calcium release in rat ventricular myocytes
title_full_unstemmed Structural variability of dyads relates to calcium release in rat ventricular myocytes
title_short Structural variability of dyads relates to calcium release in rat ventricular myocytes
title_sort structural variability of dyads relates to calcium release in rat ventricular myocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229197/
https://www.ncbi.nlm.nih.gov/pubmed/32415205
http://dx.doi.org/10.1038/s41598-020-64840-5
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