Microvilli-derived extracellular vesicles carry Hedgehog morphogenic signals for Drosophila wing imaginal disc development.


Journal

Current biology : CB
ISSN: 1879-0445
Titre abrégé: Curr Biol
Pays: England
ID NLM: 9107782

Informations de publication

Date de publication:
24 01 2022
Historique:
received: 23 11 2020
revised: 12 08 2021
accepted: 10 11 2021
pubmed: 11 12 2021
medline: 12 4 2022
entrez: 10 12 2021
Statut: ppublish

Résumé

Morphogens are secreted molecules that regulate and coordinate major developmental processes, such as cell differentiation and tissue morphogenesis. Depending on the mechanisms of secretion and the nature of their carriers, morphogens act at short and long range. We investigated the paradigmatic long-range activity of Hedgehog (Hh), a well-known morphogen, and its contribution to the growth and patterning of the Drosophila wing imaginal disc. Extracellular vesicles (EVs) contribute to Hh long-range activity; however, the nature, the site, and the mechanisms underlying the biogenesis of these vesicular carriers remain unknown. Here, through the analysis of mutants and a series of Drosophila RNAi-depleted wing imaginal discs using fluorescence and live-imaging electron microscopy, including tomography and 3D reconstruction, we demonstrate that microvilli of the wing imaginal disc epithelium are the site of generation of small EVs that transport Hh across the tissue. Further, we show that the Prominin-like (PromL) protein is critical for microvilli integrity. Together with actin cytoskeleton and membrane phospholipids, PromL maintains microvilli architecture that is essential to promote its secretory function. Importantly, the distribution of Hh to microvilli and its release via these EVs contribute to the proper morphogenesis of the wing imaginal disc. Our results demonstrate that microvilli-derived EVs are carriers for Hh long-range signaling in vivo. By establishing that members of the Prominin protein family are key determinants of microvilli formation and integrity, our findings support the view that microvilli-derived EVs conveying Hh may provide a means for exchanging signaling cues of high significance in tissue development and cancer.

Identifiants

pubmed: 34890558
pii: S0960-9822(21)01547-5
doi: 10.1016/j.cub.2021.11.023
pii:
doi:

Substances chimiques

AC133 Antigen 0
Drosophila Proteins 0
Hedgehog Proteins 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

361-373.e6

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Ilse Hurbain (I)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France.

Anne-Sophie Macé (AS)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France.

Maryse Romao (M)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France.

Elodie Prince (E)

Université Côte d'Azur, UMR7277 CNRS, Inserm U1091, Institute of Biology Valrose (iBV), Parc Valrose, 06108 Nice Cedex 2, France.

Lucie Sengmanivong (L)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France.

Laurent Ruel (L)

Université Côte d'Azur, UMR7277 CNRS, Inserm U1091, Institute of Biology Valrose (iBV), Parc Valrose, 06108 Nice Cedex 2, France.

Renata Basto (R)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France.

Pascal P Thérond (PP)

Université Côte d'Azur, UMR7277 CNRS, Inserm U1091, Institute of Biology Valrose (iBV), Parc Valrose, 06108 Nice Cedex 2, France.

Graça Raposo (G)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France.

Gisela D'Angelo (G)

Institut Curie, PSL Research University, CNRS, UMR144, 26 rue d'Ulm, 75248 Paris Cedex 05, France; Institut Curie, PSL Research University, CNRS, UMR144, Cell and Tissue Imaging Facility (PICT-IBiSA), 26, rue d'Ulm, 75248 Paris Cedex 05, France. Electronic address: gisela.dangelo@curie.fr.

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