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Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes
Analysis of the spatio-temporal distribution of calcium sparks showed a preferential increase in sparks near the sarcolemma in atrial myocytes from patients with atrial fibrillation (AF), linked to higher ryanodine receptor (RyR2) phosphorylation at s2808 and lower calsequestrin-2 levels. Mathematic...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911326/ https://www.ncbi.nlm.nih.gov/pubmed/36777175 http://dx.doi.org/10.1016/j.jacbts.2022.07.013 |
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author | Tarifa, Carmen Vallmitjana, Alexander Jiménez-Sábado, Verónica Marchena, Miquel Llach, Anna Herraiz-Martínez, Adela Godoy-Marín, Héctor Nolla-Colomer, Carme Ginel, Antonino Viñolas, Xavier Montiel, José Ciruela, Francisco Echebarria, Blas Benítez, Raúl Cinca, Juan Hove-Madsen, Leif |
author_facet | Tarifa, Carmen Vallmitjana, Alexander Jiménez-Sábado, Verónica Marchena, Miquel Llach, Anna Herraiz-Martínez, Adela Godoy-Marín, Héctor Nolla-Colomer, Carme Ginel, Antonino Viñolas, Xavier Montiel, José Ciruela, Francisco Echebarria, Blas Benítez, Raúl Cinca, Juan Hove-Madsen, Leif |
author_sort | Tarifa, Carmen |
collection | PubMed |
description | Analysis of the spatio-temporal distribution of calcium sparks showed a preferential increase in sparks near the sarcolemma in atrial myocytes from patients with atrial fibrillation (AF), linked to higher ryanodine receptor (RyR2) phosphorylation at s2808 and lower calsequestrin-2 levels. Mathematical modeling, incorporating modulation of RyR2 gating, showed that only the observed combinations of RyR2 phosphorylation and calsequestrin-2 levels can account for the spatio-temporal distribution of sparks in patients with and without AF. Furthermore, we demonstrate that preferential calcium release near the sarcolemma is key to a higher incidence and amplitude of afterdepolarizations in atrial myocytes from patients with AF. |
format | Online Article Text |
id | pubmed-9911326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-99113262023-02-11 Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes Tarifa, Carmen Vallmitjana, Alexander Jiménez-Sábado, Verónica Marchena, Miquel Llach, Anna Herraiz-Martínez, Adela Godoy-Marín, Héctor Nolla-Colomer, Carme Ginel, Antonino Viñolas, Xavier Montiel, José Ciruela, Francisco Echebarria, Blas Benítez, Raúl Cinca, Juan Hove-Madsen, Leif JACC Basic Transl Sci Original Research - Clinical Analysis of the spatio-temporal distribution of calcium sparks showed a preferential increase in sparks near the sarcolemma in atrial myocytes from patients with atrial fibrillation (AF), linked to higher ryanodine receptor (RyR2) phosphorylation at s2808 and lower calsequestrin-2 levels. Mathematical modeling, incorporating modulation of RyR2 gating, showed that only the observed combinations of RyR2 phosphorylation and calsequestrin-2 levels can account for the spatio-temporal distribution of sparks in patients with and without AF. Furthermore, we demonstrate that preferential calcium release near the sarcolemma is key to a higher incidence and amplitude of afterdepolarizations in atrial myocytes from patients with AF. Elsevier 2022-11-23 /pmc/articles/PMC9911326/ /pubmed/36777175 http://dx.doi.org/10.1016/j.jacbts.2022.07.013 Text en © 2022 Published by Elsevier on behalf of the American College of Cardiology Foundation. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research - Clinical Tarifa, Carmen Vallmitjana, Alexander Jiménez-Sábado, Verónica Marchena, Miquel Llach, Anna Herraiz-Martínez, Adela Godoy-Marín, Héctor Nolla-Colomer, Carme Ginel, Antonino Viñolas, Xavier Montiel, José Ciruela, Francisco Echebarria, Blas Benítez, Raúl Cinca, Juan Hove-Madsen, Leif Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title | Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title_full | Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title_fullStr | Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title_full_unstemmed | Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title_short | Spatial Distribution of Calcium Sparks Determines Their Ability to Induce Afterdepolarizations in Human Atrial Myocytes |
title_sort | spatial distribution of calcium sparks determines their ability to induce afterdepolarizations in human atrial myocytes |
topic | Original Research - Clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9911326/ https://www.ncbi.nlm.nih.gov/pubmed/36777175 http://dx.doi.org/10.1016/j.jacbts.2022.07.013 |
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