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

被引:92
作者
Bowling, Sarah [1 ,2 ,3 ]
Di Gregorio, Aida [1 ]
Sancho, Margarida [1 ]
Pozzi, Sara [4 ]
Aarts, Marieke [2 ,3 ]
Signore, Massimo [4 ]
Schneider, Michael D. [1 ]
Barbera, Juan Pedro Martinez [4 ]
Gil, Jesus [2 ,3 ]
Rodriguez, Tristan A. [1 ]
机构
[1] Imperial Coll London, Imperial Ctr Translat & Expt Med, Natl Heart & Lung Inst, British Heart Fdn Ctr Res Excellence, Hammersmith Hosp Campus,Du Cane Rd, London W12 0NN, England
[2] MRC London Inst Med Sci LMS, Cell Proliferat Grp, Du Cane Rd, London W12 0NN, England
[3] Imperial Coll London, Fac Med, ICS, Cell Proliferat Grp, Du Cane Rd, London W12 0NN, England
[4] UCL Great Ormond St Inst Child Hlth, Newlife Birth Defects Res Ctr, Dev Biol & Canc Programme, 30 Guilford St, London WC1N, England
基金
英国医学研究理事会;
关键词
STEM-CELLS; PREIMPLANTATION EMBRYOS; APOPTOTIC THRESHOLD; HEMATOPOIETIC STEM; C-MYC; MICE; DROSOPHILA; GROWTH; DIFFERENTIATION; PLURIPOTENCY;
D O I
10.1038/s41467-018-04167-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:12
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