Multi-view confocal microscopy enables multiple organ and whole organism live-imaging.


Journal

Development (Cambridge, England)
ISSN: 1477-9129
Titre abrégé: Development
Pays: England
ID NLM: 8701744

Informations de publication

Date de publication:
15 02 2022
Historique:
received: 04 05 2021
accepted: 13 01 2022
pubmed: 25 1 2022
medline: 9 3 2022
entrez: 24 1 2022
Statut: ppublish

Résumé

Understanding how development is coordinated in multiple tissues and gives rise to fully functional organs or whole organisms necessitates microscopy tools. Over the last decade numerous advances have been made in live-imaging, enabling high resolution imaging of whole organisms at cellular resolution. Yet, these advances mainly rely on mounting the specimen in agarose or aqueous solutions, precluding imaging of organisms whose oxygen uptake depends on ventilation. Here, we implemented a multi-view multi-scale microscopy strategy based on confocal spinning disk microscopy, called Multi-View confocal microScopy (MuViScopy). MuViScopy enables live-imaging of multiple organs with cellular resolution using sample rotation and confocal imaging without the need of sample embedding. We illustrate the capacity of MuViScopy by live-imaging Drosophila melanogaster pupal development throughout metamorphosis, highlighting how internal organs are formed and multiple organ development is coordinated. We foresee that MuViScopy will open the path to better understand developmental processes at the whole organism scale in living systems that require gas exchange by ventilation.

Identifiants

pubmed: 35072204
pii: 274464
doi: 10.1242/dev.199760
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : European Research Council
ID : 340784
Pays : International

Informations de copyright

© 2022. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interests The authors declare no competing or financial interests.

Auteurs

Olivier Leroy (O)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

Eric van Leen (E)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

Philippe Girard (P)

Université de Paris, CNRS UMR7592, Institut Jacques Monod and Faculty of Basic and Biomedical Sciences, 75006, Paris, France.

Aurélien Villedieu (A)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

Christian Hubert (C)

Errol Laser, 94100, Saint-Maur-des-Fossés, France.

Floris Bosveld (F)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

Yohanns Bellaïche (Y)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

Olivier Renaud (O)

Institut Curie, Université PSL, Sorbonne Université, CNRS UMR3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.

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Classifications MeSH