4.8 Article

Chronic activation of JNK JAK/STAT and oxidative stress signalling causes the loser cell status

Journal

NATURE COMMUNICATIONS
Volume 8, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-017-00145-y

Keywords

-

Funding

  1. Cancer Research UK Programme Grant [A12460]
  2. Royal Society University Research fellowship [UF0905080]
  3. Wellcome Trust [092096]
  4. CRUK [C6946/A14492]
  5. Alzheimers Research UK [ARUK-CJC2015, ARUK-test2018-000] Funding Source: researchfish
  6. Cancer Research UK [12460] Funding Source: researchfish
  7. Medical Research Council [MC_PC_12009] Funding Source: researchfish

Ask authors/readers for more resources

Cell competition is a form of cell interaction that causes the elimination of less fit cells, or losers, by wild-type (WT) cells, influencing overall tissue health. Several mutations can cause cells to become losers; however, it is not known how. Here we show that Drosophila wing disc cells carrying functionally unrelated loser mutations (Minute and mahjong) display the common activation of multiple stress signalling pathways before cell competition and find that these pathways collectively account for the loser status. We find that JNK signalling inhibits the growth of losers, while JAK/STAT signalling promotes competition-induced winner cell proliferation. Furthermore, we show that losers display oxidative stress response activation and, strikingly, that activation of this pathway alone, by Nrf2 overexpression, is sufficient to prime cells for their elimination by WT neighbours. Since oxidative stress and Nrf2 are linked to several diseases, cell competition may occur in a number of pathological conditions.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available