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蛋白毒性应激是失败者状态和细胞竞争的驱动因素。

Proteotoxic stress is a driver of the loser status and cell competition.

机构信息

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.

The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge, UK.

出版信息

Nat Cell Biol. 2021 Feb;23(2):136-146. doi: 10.1038/s41556-020-00627-0. Epub 2021 Jan 25.

Abstract

Cell competition allows winner cells to eliminate less fit loser cells in tissues. In Minute cell competition, cells with a heterozygous mutation in ribosome genes, such as RpS3 cells, are eliminated by wild-type cells. How cells are primed as losers is partially understood and it has been proposed that reduced translation underpins the loser status of ribosome mutant, or Minute, cells. Here, using Drosophila, we show that reduced translation does not cause cell competition. Instead, we identify proteotoxic stress as the underlying cause of the loser status for Minute competition and competition induced by mahjong, an unrelated loser gene. RpS3 cells exhibit reduced autophagic and proteasomal flux, accumulate protein aggregates and can be rescued from competition by improving their proteostasis. Conversely, inducing proteotoxic stress is sufficient to turn otherwise wild-type cells into losers. Thus, we propose that tissues may preserve their health through a proteostasis-based mechanism of cell competition and cell selection.

摘要

细胞竞争允许优势细胞消除组织中适应性较差的劣势细胞。在微小细胞竞争中,核糖体基因杂合突变的细胞(如 RpS3 细胞)会被野生型细胞消除。细胞如何被预先设定为劣势细胞部分被理解,据推测,翻译减少是核糖体突变体或微小细胞劣势状态的基础。在这里,我们使用果蝇表明,翻译减少不会引起细胞竞争。相反,我们发现蛋白毒性应激是微小竞争和由 mahjong 诱导的竞争中劣势细胞的潜在原因,后者是一个不相关的劣势基因。RpS3 细胞表现出自噬和蛋白酶体通量减少,积累蛋白聚集体,并可以通过改善其蛋白稳态从竞争中恢复。相反,诱导蛋白毒性应激足以使原本野生型的细胞变成劣势细胞。因此,我们提出组织可能通过基于蛋白稳态的细胞竞争和细胞选择机制来保持其健康。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aed/7116823/a0bc222c2989/EMS114929-f007.jpg

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