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Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease
Rapid release of calcium from internal stores via ryanodine receptors (RyRs) is one of the fastest types of cytoplasmic second messenger signalling in excitable cells. In the heart, rapid summation of the elementary events of calcium release, 'calcium sparks', determine the contraction of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205181/ https://www.ncbi.nlm.nih.gov/pubmed/37220792 http://dx.doi.org/10.1098/rsob.230045 |
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author | Hurley, Miriam E. White, Ed Sheard, Thomas M. D. Steele, Derek Jayasinghe, Izzy |
author_facet | Hurley, Miriam E. White, Ed Sheard, Thomas M. D. Steele, Derek Jayasinghe, Izzy |
author_sort | Hurley, Miriam E. |
collection | PubMed |
description | Rapid release of calcium from internal stores via ryanodine receptors (RyRs) is one of the fastest types of cytoplasmic second messenger signalling in excitable cells. In the heart, rapid summation of the elementary events of calcium release, 'calcium sparks', determine the contraction of the myocardium. We adapted a correlative super-resolution microscopy protocol to correlate sub-plasmalemmal spontaneous calcium sparks in rat right ventricular myocytes with the local nanoscale RyR2 positions. This revealed a steep relationship between the integral of a calcium spark and the sum of the local RyR2s. Segmentation of recurring spark sites showed evidence of repeated and triggered saltatory activation of multiple local RyR2 clusters. In myocytes taken from failing right ventricles, RyR2 clusters themselves showed a dissipated morphology and fragmented (smaller) clusters. They also featured greater heterogeneity in both the spark properties and the relationship between the integral of the calcium spark and the local ensemble of RyR2s. While fragmented (smaller) RyR2 clusters were rarely observed directly underlying the larger sparks or the recurring spark sites, local interrogation of the channel-to-channel distances confirmed a clear link between the positions of each calcium spark and the tight, non-random clustering of the local RyR2 in both healthy and failing ventricles. |
format | Online Article Text |
id | pubmed-10205181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-102051812023-05-24 Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease Hurley, Miriam E. White, Ed Sheard, Thomas M. D. Steele, Derek Jayasinghe, Izzy Open Biol Research Rapid release of calcium from internal stores via ryanodine receptors (RyRs) is one of the fastest types of cytoplasmic second messenger signalling in excitable cells. In the heart, rapid summation of the elementary events of calcium release, 'calcium sparks', determine the contraction of the myocardium. We adapted a correlative super-resolution microscopy protocol to correlate sub-plasmalemmal spontaneous calcium sparks in rat right ventricular myocytes with the local nanoscale RyR2 positions. This revealed a steep relationship between the integral of a calcium spark and the sum of the local RyR2s. Segmentation of recurring spark sites showed evidence of repeated and triggered saltatory activation of multiple local RyR2 clusters. In myocytes taken from failing right ventricles, RyR2 clusters themselves showed a dissipated morphology and fragmented (smaller) clusters. They also featured greater heterogeneity in both the spark properties and the relationship between the integral of the calcium spark and the local ensemble of RyR2s. While fragmented (smaller) RyR2 clusters were rarely observed directly underlying the larger sparks or the recurring spark sites, local interrogation of the channel-to-channel distances confirmed a clear link between the positions of each calcium spark and the tight, non-random clustering of the local RyR2 in both healthy and failing ventricles. The Royal Society 2023-05-24 /pmc/articles/PMC10205181/ /pubmed/37220792 http://dx.doi.org/10.1098/rsob.230045 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Hurley, Miriam E. White, Ed Sheard, Thomas M. D. Steele, Derek Jayasinghe, Izzy Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title | Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title_full | Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title_fullStr | Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title_full_unstemmed | Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title_short | Correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
title_sort | correlative super-resolution analysis of cardiac calcium sparks and their molecular origins in health and disease |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10205181/ https://www.ncbi.nlm.nih.gov/pubmed/37220792 http://dx.doi.org/10.1098/rsob.230045 |
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