Mechanical cell competition kills cells via induction of lethal p53 levels

Cell competition is a quality control mechanism that eliminates unfit cells. How cells compete is poorly understood, but it is generally accepted that molecular exchange between cells signals elimination of unfit cells. Here we report an orthogonal mechanism of cell competition, whereby cells compet...

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Veröffentlicht in:Nature communications 2016-04, Vol.7 (1), p.11373-11373, Article 11373
Hauptverfasser: Wagstaff, Laura, Goschorska, Maja, Kozyrska, Kasia, Duclos, Guillaume, Kucinski, Iwo, Chessel, Anatole, Hampton-O’Neil, Lea, Bradshaw, Charles R., Allen, George E., Rawlins, Emma L., Silberzan, Pascal, Carazo Salas, Rafael E., Piddini, Eugenia
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Sprache:eng
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Zusammenfassung:Cell competition is a quality control mechanism that eliminates unfit cells. How cells compete is poorly understood, but it is generally accepted that molecular exchange between cells signals elimination of unfit cells. Here we report an orthogonal mechanism of cell competition, whereby cells compete through mechanical insults. We show that MDCK cells silenced for the polarity gene scribble ( scrib KD ) are hypersensitive to compaction, that interaction with wild-type cells causes their compaction and that crowding is sufficient for scrib KD cell elimination. Importantly, we show that elevation of the tumour suppressor p53 is necessary and sufficient for crowding hypersensitivity. Compaction, via activation of Rho-associated kinase (ROCK) and the stress kinase p38, leads to further p53 elevation, causing cell death. Thus, in addition to molecules, cells use mechanical means to compete. Given the involvement of p53, compaction hypersensitivity may be widespread among damaged cells and offers an additional route to eliminate unfit cells. Cell competition is a quality control mechanism to eliminate unfit cells. Here the authors show that physical compaction of less fit cells surrounded by healthy neighbours leads to increased expression of tumour suppressor p53 in the compacted cells, causing cell death.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms11373