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A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish

Endothelial tip cells (ETCs) located at growing blood vessels display high morphological dynamics and associated intracellular Ca(2+) activities with different spatiotemporal patterns during migration. Examining the Ca(2+) activity and morphological dynamics of ETCs will provide an insight for under...

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Detalles Bibliográficos
Autores principales: Liu, Ting-ting, Hou, Han, Du, Jiu-lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982748/
https://www.ncbi.nlm.nih.gov/pubmed/33778782
http://dx.doi.org/10.1016/j.xpro.2021.100388
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author Liu, Ting-ting
Hou, Han
Du, Jiu-lin
author_facet Liu, Ting-ting
Hou, Han
Du, Jiu-lin
author_sort Liu, Ting-ting
collection PubMed
description Endothelial tip cells (ETCs) located at growing blood vessels display high morphological dynamics and associated intracellular Ca(2+) activities with different spatiotemporal patterns during migration. Examining the Ca(2+) activity and morphological dynamics of ETCs will provide an insight for understanding the mechanism of vascular development in organs, including the brain. Here, we describe a method for simultaneous monitoring and relevant analysis of the Ca(2+) activity and morphology of growing brain ETCs in larval zebrafish. For complete details on the use and execution of this protocol, please refer to Liu et al. (2020).
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spelling pubmed-79827482021-03-25 A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish Liu, Ting-ting Hou, Han Du, Jiu-lin STAR Protoc Protocol Endothelial tip cells (ETCs) located at growing blood vessels display high morphological dynamics and associated intracellular Ca(2+) activities with different spatiotemporal patterns during migration. Examining the Ca(2+) activity and morphological dynamics of ETCs will provide an insight for understanding the mechanism of vascular development in organs, including the brain. Here, we describe a method for simultaneous monitoring and relevant analysis of the Ca(2+) activity and morphology of growing brain ETCs in larval zebrafish. For complete details on the use and execution of this protocol, please refer to Liu et al. (2020). Elsevier 2021-03-18 /pmc/articles/PMC7982748/ /pubmed/33778782 http://dx.doi.org/10.1016/j.xpro.2021.100388 Text en © 2021 The Author(s) http://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 Protocol
Liu, Ting-ting
Hou, Han
Du, Jiu-lin
A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title_full A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title_fullStr A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title_full_unstemmed A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title_short A protocol for simultaneous Ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
title_sort protocol for simultaneous ca(2+) and morphology imaging of brain endothelial tip cells in larval zebrafish
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982748/
https://www.ncbi.nlm.nih.gov/pubmed/33778782
http://dx.doi.org/10.1016/j.xpro.2021.100388
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