A live-imaging protocol to track cell movement in the Xenopus embryo

Summary: Tracking individual cell movement during development is challenging, particularly in tissues subjected to major remodeling. Currently, most live imaging techniques in Xenopus are limited to tissue explants and/or to superficial cells. We describe here a protocol to track immature multicilia...

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Autores principales: Alexandre Chuyen, Fabrice Daian, Andrea Pasini, Laurent Kodjabachian
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/502d4d7a2c6e4366ba618e1de906eded
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spelling oai:doaj.org-article:502d4d7a2c6e4366ba618e1de906eded2021-11-04T04:39:49ZA live-imaging protocol to track cell movement in the Xenopus embryo2666-166710.1016/j.xpro.2021.100928https://doaj.org/article/502d4d7a2c6e4366ba618e1de906eded2021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666166721006341https://doaj.org/toc/2666-1667Summary: Tracking individual cell movement during development is challenging, particularly in tissues subjected to major remodeling. Currently, most live imaging techniques in Xenopus are limited to tissue explants and/or to superficial cells. We describe here a protocol to track immature multiciliated cells (MCCs) moving within the inner epidermal layer of a whole embryo. In addition, we present a data processing protocol to uncouple the movements of individual cells from the coplanar drifts of the tissue in which they are embedded.For complete details on the use and execution of this protocol, please refer to Chuyen et al. (2021).Alexandre ChuyenFabrice DaianAndrea PasiniLaurent KodjabachianElsevierarticleCell BiologyDevelopmental biologyMicroscopyModel OrganismsScience (General)Q1-390ENSTAR Protocols, Vol 2, Iss 4, Pp 100928- (2021)
institution DOAJ
collection DOAJ
language EN
topic Cell Biology
Developmental biology
Microscopy
Model Organisms
Science (General)
Q1-390
spellingShingle Cell Biology
Developmental biology
Microscopy
Model Organisms
Science (General)
Q1-390
Alexandre Chuyen
Fabrice Daian
Andrea Pasini
Laurent Kodjabachian
A live-imaging protocol to track cell movement in the Xenopus embryo
description Summary: Tracking individual cell movement during development is challenging, particularly in tissues subjected to major remodeling. Currently, most live imaging techniques in Xenopus are limited to tissue explants and/or to superficial cells. We describe here a protocol to track immature multiciliated cells (MCCs) moving within the inner epidermal layer of a whole embryo. In addition, we present a data processing protocol to uncouple the movements of individual cells from the coplanar drifts of the tissue in which they are embedded.For complete details on the use and execution of this protocol, please refer to Chuyen et al. (2021).
format article
author Alexandre Chuyen
Fabrice Daian
Andrea Pasini
Laurent Kodjabachian
author_facet Alexandre Chuyen
Fabrice Daian
Andrea Pasini
Laurent Kodjabachian
author_sort Alexandre Chuyen
title A live-imaging protocol to track cell movement in the Xenopus embryo
title_short A live-imaging protocol to track cell movement in the Xenopus embryo
title_full A live-imaging protocol to track cell movement in the Xenopus embryo
title_fullStr A live-imaging protocol to track cell movement in the Xenopus embryo
title_full_unstemmed A live-imaging protocol to track cell movement in the Xenopus embryo
title_sort live-imaging protocol to track cell movement in the xenopus embryo
publisher Elsevier
publishDate 2021
url https://doaj.org/article/502d4d7a2c6e4366ba618e1de906eded
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