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Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection

Adipocytes have many functions in various tissues beyond energy storage, including regulating metabolism, growth, and immunity. However, little is known about their role in wound healing. Here we use live imaging of fat body cells, the equivalent of vertebrate adipocytes in Drosophila, to investigat...

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Detalles Bibliográficos
Autores principales: Franz, Anna, Wood, Will, Martin, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113741/
https://www.ncbi.nlm.nih.gov/pubmed/29486196
http://dx.doi.org/10.1016/j.devcel.2018.01.026
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author Franz, Anna
Wood, Will
Martin, Paul
author_facet Franz, Anna
Wood, Will
Martin, Paul
author_sort Franz, Anna
collection PubMed
description Adipocytes have many functions in various tissues beyond energy storage, including regulating metabolism, growth, and immunity. However, little is known about their role in wound healing. Here we use live imaging of fat body cells, the equivalent of vertebrate adipocytes in Drosophila, to investigate their potential behaviors and functions following skin wounding. We find that pupal fat body cells are not immotile, as previously presumed, but actively migrate to wounds using an unusual adhesion-independent, actomyosin-driven, peristaltic mode of motility. Once at the wound, fat body cells collaborate with hemocytes, Drosophila macrophages, to clear the wound of cell debris; they also tightly seal the epithelial wound gap and locally release antimicrobial peptides to fight wound infection. Thus, fat body cells are motile cells, enabling them to migrate to wounds to undertake several local functions needed to drive wound repair and prevent infections.
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spelling pubmed-61137412018-08-30 Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection Franz, Anna Wood, Will Martin, Paul Dev Cell Article Adipocytes have many functions in various tissues beyond energy storage, including regulating metabolism, growth, and immunity. However, little is known about their role in wound healing. Here we use live imaging of fat body cells, the equivalent of vertebrate adipocytes in Drosophila, to investigate their potential behaviors and functions following skin wounding. We find that pupal fat body cells are not immotile, as previously presumed, but actively migrate to wounds using an unusual adhesion-independent, actomyosin-driven, peristaltic mode of motility. Once at the wound, fat body cells collaborate with hemocytes, Drosophila macrophages, to clear the wound of cell debris; they also tightly seal the epithelial wound gap and locally release antimicrobial peptides to fight wound infection. Thus, fat body cells are motile cells, enabling them to migrate to wounds to undertake several local functions needed to drive wound repair and prevent infections. Cell Press 2018-02-26 /pmc/articles/PMC6113741/ /pubmed/29486196 http://dx.doi.org/10.1016/j.devcel.2018.01.026 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Franz, Anna
Wood, Will
Martin, Paul
Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title_full Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title_fullStr Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title_full_unstemmed Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title_short Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection
title_sort fat body cells are motile and actively migrate to wounds to drive repair and prevent infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6113741/
https://www.ncbi.nlm.nih.gov/pubmed/29486196
http://dx.doi.org/10.1016/j.devcel.2018.01.026
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