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Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development

Bioelectricity is defined as endogenous electrical signaling mediated by the dynamic distribution of charged molecules. Recently, increasing evidence has revealed that cellular bioelectric signaling is critical for regulating embryonic development, regeneration, and congenital diseases. However, sys...

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Autores principales: Silic, Martin R., Dong, Ziyu, Chen, Yueyi, Kimbrough, Adam, Zhang, Guangjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688842/
https://www.ncbi.nlm.nih.gov/pubmed/36429015
http://dx.doi.org/10.3390/cells11223586
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author Silic, Martin R.
Dong, Ziyu
Chen, Yueyi
Kimbrough, Adam
Zhang, Guangjun
author_facet Silic, Martin R.
Dong, Ziyu
Chen, Yueyi
Kimbrough, Adam
Zhang, Guangjun
author_sort Silic, Martin R.
collection PubMed
description Bioelectricity is defined as endogenous electrical signaling mediated by the dynamic distribution of charged molecules. Recently, increasing evidence has revealed that cellular bioelectric signaling is critical for regulating embryonic development, regeneration, and congenital diseases. However, systematic real-time in vivo dynamic electrical activity monitoring of whole organisms has been limited, mainly due to the lack of a suitable model system and voltage measurement tools for in vivo biology. Here, we addressed this gap by utilizing a genetically stable zebrafish line, Tg (ubiquitin: ASAP1), and ASAP1 (Accelerated sensor of action potentials 1), a genetically encoded voltage indicator (GEVI). With light-sheet microscopy, we systematically investigated cell membrane potential (Vm) signals during different embryonic stages. We found cells of zebrafish embryos showed local membrane hyperpolarization at the cleavage furrows during the cleavage period of embryogenesis. This signal appeared before cytokinesis and fluctuated as it progressed. In contrast, whole-cell transient hyperpolarization was observed during the blastula and gastrula stages. These signals were generally limited to the superficial blastomere, but they could be detected within the deeper cells during the gastrulation period. Moreover, the zebrafish embryos exhibit tissue-level cell Vm signals during the segmentation period. Middle-aged somites had strong and dynamic Vm fluctuations starting at about the 12-somite stage. These embryonic stage-specific characteristic cellular bioelectric signals suggest that they might play a diverse role in zebrafish embryogenesis that could underlie human congenital diseases.
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spelling pubmed-96888422022-11-25 Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development Silic, Martin R. Dong, Ziyu Chen, Yueyi Kimbrough, Adam Zhang, Guangjun Cells Article Bioelectricity is defined as endogenous electrical signaling mediated by the dynamic distribution of charged molecules. Recently, increasing evidence has revealed that cellular bioelectric signaling is critical for regulating embryonic development, regeneration, and congenital diseases. However, systematic real-time in vivo dynamic electrical activity monitoring of whole organisms has been limited, mainly due to the lack of a suitable model system and voltage measurement tools for in vivo biology. Here, we addressed this gap by utilizing a genetically stable zebrafish line, Tg (ubiquitin: ASAP1), and ASAP1 (Accelerated sensor of action potentials 1), a genetically encoded voltage indicator (GEVI). With light-sheet microscopy, we systematically investigated cell membrane potential (Vm) signals during different embryonic stages. We found cells of zebrafish embryos showed local membrane hyperpolarization at the cleavage furrows during the cleavage period of embryogenesis. This signal appeared before cytokinesis and fluctuated as it progressed. In contrast, whole-cell transient hyperpolarization was observed during the blastula and gastrula stages. These signals were generally limited to the superficial blastomere, but they could be detected within the deeper cells during the gastrulation period. Moreover, the zebrafish embryos exhibit tissue-level cell Vm signals during the segmentation period. Middle-aged somites had strong and dynamic Vm fluctuations starting at about the 12-somite stage. These embryonic stage-specific characteristic cellular bioelectric signals suggest that they might play a diverse role in zebrafish embryogenesis that could underlie human congenital diseases. MDPI 2022-11-12 /pmc/articles/PMC9688842/ /pubmed/36429015 http://dx.doi.org/10.3390/cells11223586 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Silic, Martin R.
Dong, Ziyu
Chen, Yueyi
Kimbrough, Adam
Zhang, Guangjun
Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title_full Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title_fullStr Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title_full_unstemmed Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title_short Zebrafish Embryos Display Characteristic Bioelectric Signals during Early Development
title_sort zebrafish embryos display characteristic bioelectric signals during early development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688842/
https://www.ncbi.nlm.nih.gov/pubmed/36429015
http://dx.doi.org/10.3390/cells11223586
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