4.8 Article

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

Journal

CELL REPORTS
Volume 37, Issue 2, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2021.109827

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Funding

  1. Bloomington Drosophila Stock Center (National Institutes of Health [NIH]) [P40-OD018537]
  2. Harvard Medical School TRiP Center (NIH National Institute of General Medical Sciences [NIGMS]) [R01-GM084947]
  3. Maine IDeA Network of Biomedical Research Excellence (NIH NIGMS) [GM103423]
  4. Bret Judson and the Boston College Imaging Core
  5. MDI Biological Laboratory, Boston College
  6. NIH NIGMS [R35-GM124691, P20-GM104318]

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Polyploid cells generated in response to injury in adult Drosophila epithelium alter tissue mechanics by enhancing epithelial tension, which helps maintain abdominal movements and potentially compensates for lost tissue tension. The activation and upregulation of nonmuscle myosin II in wound-induced polyploid cells persist after healing completes.
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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