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P53 和 mTOR 信号通过早期胚胎发育过程中的细胞竞争决定适应性选择。

P53 and mTOR signalling determine fitness selection through cell competition during early mouse embryonic development.

机构信息

British Heart Foundation Centre for Research Excellence, National Heart and Lung Institute, Imperial Centre for Translational and Experimental Medicine, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK.

Cell Proliferation Group, MRC London Institute of Medical Sciences (LMS), Du Cane Road, London, W12 0NN, UK.

出版信息

Nat Commun. 2018 May 2;9(1):1763. doi: 10.1038/s41467-018-04167-y.

Abstract

Ensuring the fitness of the pluripotent cells that will contribute to future development is important both for the integrity of the germline and for proper embryogenesis. Consequently, it is becoming increasingly apparent that pluripotent cells can compare their fitness levels and signal the elimination of those cells that are less fit than their neighbours. In mammals the nature of the pathways that communicate fitness remain largely unknown. Here we identify that in the early mouse embryo and upon exit from naive pluripotency, the confrontation of cells with different fitness levels leads to an inhibition of mTOR signalling in the less fit cell type, causing its elimination. We show that during this process, p53 acts upstream of mTOR and is required to repress its activity. Finally, we demonstrate that during normal development around 35% of cells are eliminated by this pathway, highlighting the importance of this mechanism for embryonic development.

摘要

确保将为未来发育做出贡献的多能细胞具有良好的状态,这对于生殖系的完整性和胚胎正常发育都很重要。因此,多能细胞能够比较它们的健康水平并发出信号消除那些比其邻居状态差的细胞,这一点变得越来越明显。在哺乳动物中,沟通健康水平的途径的性质在很大程度上仍是未知的。在这里,我们鉴定出在早期小鼠胚胎中和在退出原始多能性之后,细胞与不同健康水平的对抗会导致在状态较差的细胞类型中抑制 mTOR 信号,从而导致其消除。我们表明,在此过程中,p53 在 mTOR 的上游起作用,并且需要抑制其活性。最后,我们证明在正常发育过程中,约有 35%的细胞通过该途径被消除,这突显了该机制对于胚胎发育的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ff3/5932021/c6e6c6157c53/41467_2018_4167_Fig1_HTML.jpg

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