Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes

Summary: This protocol describes how to image time and spatially resolved time lapses of Drosophila air sac primordium (ASP) cytonemes in ex vivo cultures of wing imaginal discs. It describes how to manually measure the length of cytonemes using custom-made FIJI/ImageJ tools, and to analyze data usi...

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Main Authors: Guilherme O. Barbosa, Thomas B. Kornberg
Format: Article
Language:English
Published: Elsevier 2022-03-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166722000181
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author Guilherme O. Barbosa
Thomas B. Kornberg
author_facet Guilherme O. Barbosa
Thomas B. Kornberg
author_sort Guilherme O. Barbosa
collection DOAJ
description Summary: This protocol describes how to image time and spatially resolved time lapses of Drosophila air sac primordium (ASP) cytonemes in ex vivo cultures of wing imaginal discs. It describes how to manually measure the length of cytonemes using custom-made FIJI/ImageJ tools, and to analyze data using R/R-Studios pipeline. It can also be used for studies of cell division, organelle localization, and protein trafficking as well as other cellular materials that can be fluorescently tagged and imaged with minimal phototoxicity.
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spelling doaj.art-af61ddfa51ec4e52a4eee157e65932382022-12-21T23:50:45ZengElsevierSTAR Protocols2666-16672022-03-0131101138Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemesGuilherme O. Barbosa0Thomas B. Kornberg1Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA; Corresponding authorCardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA; Corresponding authorSummary: This protocol describes how to image time and spatially resolved time lapses of Drosophila air sac primordium (ASP) cytonemes in ex vivo cultures of wing imaginal discs. It describes how to manually measure the length of cytonemes using custom-made FIJI/ImageJ tools, and to analyze data using R/R-Studios pipeline. It can also be used for studies of cell division, organelle localization, and protein trafficking as well as other cellular materials that can be fluorescently tagged and imaged with minimal phototoxicity.http://www.sciencedirect.com/science/article/pii/S2666166722000181Cell BiologyDevelopmental biologyMicroscopyModel Organisms
spellingShingle Guilherme O. Barbosa
Thomas B. Kornberg
Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
STAR Protocols
Cell Biology
Developmental biology
Microscopy
Model Organisms
title Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
title_full Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
title_fullStr Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
title_full_unstemmed Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
title_short Protocol for ex vivo time lapse imaging of Drosophila melanogaster cytonemes
title_sort protocol for ex vivo time lapse imaging of drosophila melanogaster cytonemes
topic Cell Biology
Developmental biology
Microscopy
Model Organisms
url http://www.sciencedirect.com/science/article/pii/S2666166722000181
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