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Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging

The spatio-temporal properties of Ca(2+) transients during excitation-contraction coupling and elementary Ca(2+) release events (Ca(2+) sparks) were studied in atrial and ventricular myocytes with ultra-fast confocal microscopy using a Zeiss LSM 5 LIVE system that allows sampling rates of up to 60 k...

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Autores principales: Shkryl, Vyacheslav M., Blatter, Lothar A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630194/
https://www.ncbi.nlm.nih.gov/pubmed/23637847
http://dx.doi.org/10.1371/journal.pone.0061525
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author Shkryl, Vyacheslav M.
Blatter, Lothar A.
author_facet Shkryl, Vyacheslav M.
Blatter, Lothar A.
author_sort Shkryl, Vyacheslav M.
collection PubMed
description The spatio-temporal properties of Ca(2+) transients during excitation-contraction coupling and elementary Ca(2+) release events (Ca(2+) sparks) were studied in atrial and ventricular myocytes with ultra-fast confocal microscopy using a Zeiss LSM 5 LIVE system that allows sampling rates of up to 60 kHz. Ca(2+) sparks which originated from subsarcolemmal junctional sarcoplasmic reticulum (j-SR) release sites in atrial myocytes were anisotropic and elongated in the longitudinal direction of the cell. Ca(2+) sparks in atrial cells originating from non-junctional SR and in ventricular myocytes were symmetrical. Ca(2+) spark recording in line scan mode at 40,000 lines/s uncovered step-like increases of [Ca(2+)](i). 2-D imaging of Ca(2+) transients revealed an asynchronous activation of release sites and allowed the sequential recording of Ca(2+) entry through surface membrane Ca(2+) channels and subsequent activation of Ca(2+)-induced Ca(2+) release. With a latency of 2.5 ms after application of an electrical stimulus, Ca(2+) entry could be detected that was followed by SR Ca(2+) release after an additional 3 ms delay. Maximum Ca(2+) release was observed 4 ms after the beginning of release. The timing of Ca(2+) entry and release was confirmed by simultaneous [Ca(2+)](i) and membrane current measurements using the whole cell voltage-clamp technique. In atrial cells activation of discrete individual release sites of the j-SR led to spatially restricted Ca(2+) release events that fused into a peripheral ring of elevated [Ca(2+)](i) that subsequently propagated in a wave-like fashion towards the center of the cell. In ventricular myocytes asynchronous Ca(2+) release signals from discrete sites with no preferential subcellular location preceded the whole-cell Ca(2+) transient. In summary, ultra-fast confocal imaging allows investigation of Ca(2+) signals with a time resolution similar to patch clamp technique, however in a less invasive fashion.
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spelling pubmed-36301942013-05-01 Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging Shkryl, Vyacheslav M. Blatter, Lothar A. PLoS One Research Article The spatio-temporal properties of Ca(2+) transients during excitation-contraction coupling and elementary Ca(2+) release events (Ca(2+) sparks) were studied in atrial and ventricular myocytes with ultra-fast confocal microscopy using a Zeiss LSM 5 LIVE system that allows sampling rates of up to 60 kHz. Ca(2+) sparks which originated from subsarcolemmal junctional sarcoplasmic reticulum (j-SR) release sites in atrial myocytes were anisotropic and elongated in the longitudinal direction of the cell. Ca(2+) sparks in atrial cells originating from non-junctional SR and in ventricular myocytes were symmetrical. Ca(2+) spark recording in line scan mode at 40,000 lines/s uncovered step-like increases of [Ca(2+)](i). 2-D imaging of Ca(2+) transients revealed an asynchronous activation of release sites and allowed the sequential recording of Ca(2+) entry through surface membrane Ca(2+) channels and subsequent activation of Ca(2+)-induced Ca(2+) release. With a latency of 2.5 ms after application of an electrical stimulus, Ca(2+) entry could be detected that was followed by SR Ca(2+) release after an additional 3 ms delay. Maximum Ca(2+) release was observed 4 ms after the beginning of release. The timing of Ca(2+) entry and release was confirmed by simultaneous [Ca(2+)](i) and membrane current measurements using the whole cell voltage-clamp technique. In atrial cells activation of discrete individual release sites of the j-SR led to spatially restricted Ca(2+) release events that fused into a peripheral ring of elevated [Ca(2+)](i) that subsequently propagated in a wave-like fashion towards the center of the cell. In ventricular myocytes asynchronous Ca(2+) release signals from discrete sites with no preferential subcellular location preceded the whole-cell Ca(2+) transient. In summary, ultra-fast confocal imaging allows investigation of Ca(2+) signals with a time resolution similar to patch clamp technique, however in a less invasive fashion. Public Library of Science 2013-04-18 /pmc/articles/PMC3630194/ /pubmed/23637847 http://dx.doi.org/10.1371/journal.pone.0061525 Text en © 2013 Shkryl, Blatter http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shkryl, Vyacheslav M.
Blatter, Lothar A.
Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title_full Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title_fullStr Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title_full_unstemmed Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title_short Ca(2+) Release Events in Cardiac Myocytes Up Close: Insights from Fast Confocal Imaging
title_sort ca(2+) release events in cardiac myocytes up close: insights from fast confocal imaging
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630194/
https://www.ncbi.nlm.nih.gov/pubmed/23637847
http://dx.doi.org/10.1371/journal.pone.0061525
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