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- W4311556634 endingPage "e1010516" @default.
- W4311556634 startingPage "e1010516" @default.
- W4311556634 abstract "Regeneration relies on cell proliferation to restore damaged tissues. Multiple signaling pathways activated by local or paracrine cues have been identified to promote regenerative proliferation. How different types of tissue damage may activate distinct signaling pathways and how these differences converge on regenerative proliferation is less well defined. To better understand how tissue damage and proliferative signals are integrated during regeneration, we investigate models of compensatory proliferation in Drosophila imaginal discs. We find that compensatory proliferation is associated with a unique cell cycle profile, which is characterized by short G1 and G2 phases and, surprisingly, by acceleration of the S-phase. S-phase acceleration can be induced by two distinct signaling signatures, aligning with inflammatory and non-inflammatory tissue damage. Specifically, non-autonomous activation of JAK/STAT and Myc in response to inflammatory damage, or local activation of Ras/ERK and Hippo/Yki in response to elevated cell death, promote accelerated nucleotide incorporation during S-phase. This previously unappreciated convergence of different damaging insults on the same regenerative cell cycle program reconciles previous conflicting observations on proliferative signaling in different tissue regeneration and tumor models." @default.
- W4311556634 created "2022-12-27" @default.
- W4311556634 creator A5007498609 @default.
- W4311556634 creator A5013538201 @default.
- W4311556634 creator A5020100572 @default.
- W4311556634 creator A5042687430 @default.
- W4311556634 creator A5042836562 @default.
- W4311556634 creator A5074555527 @default.
- W4311556634 creator A5075492275 @default.
- W4311556634 date "2022-12-15" @default.
- W4311556634 modified "2023-09-25" @default.
- W4311556634 title "Distinct signaling signatures drive compensatory proliferation via S-phase acceleration" @default.
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