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The endocycle restores tissue tension in the Drosophila abdomen post wound repair

Polyploidy frequently arises in response to injury, aging, and disease. Despite its prevalence, major gaps exist in our understanding of how polyploid cells alter tissue function. In the adult Drosophila epithelium, wound healing is dependent on the generation of multinucleated polyploid cells resul...

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Autores principales: Losick, Vicki P., Duhaime, Levi G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567445/
https://www.ncbi.nlm.nih.gov/pubmed/34644579
http://dx.doi.org/10.1016/j.celrep.2021.109827
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author Losick, Vicki P.
Duhaime, Levi G.
author_facet Losick, Vicki P.
Duhaime, Levi G.
author_sort Losick, Vicki P.
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description Polyploidy frequently arises in response to injury, aging, and disease. Despite its prevalence, major gaps exist in our understanding of how polyploid cells alter tissue function. In the adult Drosophila epithelium, wound healing is dependent on the generation of multinucleated polyploid cells resulting in a permanent change in the epithelial architecture. Here, we study how the wound-induced polyploid cells affect tissue function by altering epithelial mechanics. The mechanosensor nonmuscle myosin II is activated and upregulated in wound-induced polyploid cells and persists after healing completes. Polyploidy enhances relative epithelial tension, which is dependent on the endocycle and not cell fusion post injury. Remarkably, the enhanced epithelial tension mimics the relative tension of the lateral muscle fibers, which are permanently severed by the injury. As a result, we found that the wound-induced polyploid cells remodel the epithelium to maintain fly abdominal movements, which may help compensate for lost tissue tension.
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spelling pubmed-85674452021-11-04 The endocycle restores tissue tension in the Drosophila abdomen post wound repair Losick, Vicki P. Duhaime, Levi G. Cell Rep Article Polyploidy frequently arises in response to injury, aging, and disease. Despite its prevalence, major gaps exist in our understanding of how polyploid cells alter tissue function. In the adult Drosophila epithelium, wound healing is dependent on the generation of multinucleated polyploid cells resulting in a permanent change in the epithelial architecture. Here, we study how the wound-induced polyploid cells affect tissue function by altering epithelial mechanics. The mechanosensor nonmuscle myosin II is activated and upregulated in wound-induced polyploid cells and persists after healing completes. Polyploidy enhances relative epithelial tension, which is dependent on the endocycle and not cell fusion post injury. Remarkably, the enhanced epithelial tension mimics the relative tension of the lateral muscle fibers, which are permanently severed by the injury. As a result, we found that the wound-induced polyploid cells remodel the epithelium to maintain fly abdominal movements, which may help compensate for lost tissue tension. 2021-10-12 /pmc/articles/PMC8567445/ /pubmed/34644579 http://dx.doi.org/10.1016/j.celrep.2021.109827 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Losick, Vicki P.
Duhaime, Levi G.
The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title_full The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title_fullStr The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title_full_unstemmed The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title_short The endocycle restores tissue tension in the Drosophila abdomen post wound repair
title_sort endocycle restores tissue tension in the drosophila abdomen post wound repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567445/
https://www.ncbi.nlm.nih.gov/pubmed/34644579
http://dx.doi.org/10.1016/j.celrep.2021.109827
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