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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Elsevier
2021
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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) |
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DOAJ |
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Cell Biology Developmental biology Microscopy Model Organisms Science (General) Q1-390 |
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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 |
work_keys_str_mv |
AT alexandrechuyen aliveimagingprotocoltotrackcellmovementinthexenopusembryo AT fabricedaian aliveimagingprotocoltotrackcellmovementinthexenopusembryo AT andreapasini aliveimagingprotocoltotrackcellmovementinthexenopusembryo AT laurentkodjabachian aliveimagingprotocoltotrackcellmovementinthexenopusembryo AT alexandrechuyen liveimagingprotocoltotrackcellmovementinthexenopusembryo AT fabricedaian liveimagingprotocoltotrackcellmovementinthexenopusembryo AT andreapasini liveimagingprotocoltotrackcellmovementinthexenopusembryo AT laurentkodjabachian liveimagingprotocoltotrackcellmovementinthexenopusembryo |
_version_ |
1718445207923458048 |