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Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart

Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely challenging, due to the heart’s constant motion and a need to avoid pharmacological or phototoxic damage. Although real-time triggered imaging can computationally “freeze” the heart for 3D imaging, no previous algori...

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Autores principales: Taylor, Jonathan M., Nelson, Carl J., Bruton, Finnius A., Kaveh, Aryan, Buckley, Charlotte, Tucker, Carl S., Rossi, Adriano G., Mullins, John J., Denvir, Martin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858381/
https://www.ncbi.nlm.nih.gov/pubmed/31729395
http://dx.doi.org/10.1038/s41467-019-13112-6
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author Taylor, Jonathan M.
Nelson, Carl J.
Bruton, Finnius A.
Kaveh, Aryan
Buckley, Charlotte
Tucker, Carl S.
Rossi, Adriano G.
Mullins, John J.
Denvir, Martin A.
author_facet Taylor, Jonathan M.
Nelson, Carl J.
Bruton, Finnius A.
Kaveh, Aryan
Buckley, Charlotte
Tucker, Carl S.
Rossi, Adriano G.
Mullins, John J.
Denvir, Martin A.
author_sort Taylor, Jonathan M.
collection PubMed
description Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely challenging, due to the heart’s constant motion and a need to avoid pharmacological or phototoxic damage. Although real-time triggered imaging can computationally “freeze” the heart for 3D imaging, no previous algorithm has been able to maintain phase-lock across developmental timescales. We report a new algorithm capable of maintaining day-long phase-lock, permitting routine acquisition of synchronised 3D + time video time-lapse datasets of the beating zebrafish heart. This approach has enabled us for the first time to directly observe detailed developmental and cellular processes in the beating heart, revealing the dynamics of the immune response to injury and witnessing intriguing proliferative events that challenge the established literature on cardiac trabeculation. Our approach opens up exciting new opportunities for direct time-lapse imaging studies over a 24-hour time course, to understand the cellular mechanisms underlying cardiac development, repair and regeneration.
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spelling pubmed-68583812019-11-20 Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart Taylor, Jonathan M. Nelson, Carl J. Bruton, Finnius A. Kaveh, Aryan Buckley, Charlotte Tucker, Carl S. Rossi, Adriano G. Mullins, John J. Denvir, Martin A. Nat Commun Article Three-dimensional fluorescence time-lapse imaging of the beating heart is extremely challenging, due to the heart’s constant motion and a need to avoid pharmacological or phototoxic damage. Although real-time triggered imaging can computationally “freeze” the heart for 3D imaging, no previous algorithm has been able to maintain phase-lock across developmental timescales. We report a new algorithm capable of maintaining day-long phase-lock, permitting routine acquisition of synchronised 3D + time video time-lapse datasets of the beating zebrafish heart. This approach has enabled us for the first time to directly observe detailed developmental and cellular processes in the beating heart, revealing the dynamics of the immune response to injury and witnessing intriguing proliferative events that challenge the established literature on cardiac trabeculation. Our approach opens up exciting new opportunities for direct time-lapse imaging studies over a 24-hour time course, to understand the cellular mechanisms underlying cardiac development, repair and regeneration. Nature Publishing Group UK 2019-11-15 /pmc/articles/PMC6858381/ /pubmed/31729395 http://dx.doi.org/10.1038/s41467-019-13112-6 Text en © The Author(s) 2019 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
Taylor, Jonathan M.
Nelson, Carl J.
Bruton, Finnius A.
Kaveh, Aryan
Buckley, Charlotte
Tucker, Carl S.
Rossi, Adriano G.
Mullins, John J.
Denvir, Martin A.
Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title_full Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title_fullStr Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title_full_unstemmed Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title_short Adaptive prospective optical gating enables day-long 3D time-lapse imaging of the beating embryonic zebrafish heart
title_sort adaptive prospective optical gating enables day-long 3d time-lapse imaging of the beating embryonic zebrafish heart
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858381/
https://www.ncbi.nlm.nih.gov/pubmed/31729395
http://dx.doi.org/10.1038/s41467-019-13112-6
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