Cardiovascular Development Program, Centro Nacional de Investigaciones Cardiovasculares, CNIC, Madrid 28029, Spain.
Cellomics Unit, Centro Nacional de Investigaciones Cardiovasculares, CNIC, Madrid 28029, Spain.
Dev Cell. 2017 Sep 25;42(6):585-599.e4. doi: 10.1016/j.devcel.2017.08.011. Epub 2017 Sep 14.
The mammalian epiblast is formed by pluripotent cells able to differentiate into all tissues of the new individual. In their progression to differentiation, epiblast cells and their in vitro counterparts, embryonic stem cells (ESCs), transit from naive pluripotency through a differentiation-primed pluripotent state. During these events, epiblast cells and ESCs are prone to death, driven by competition between Myc-high cells (winners) and Myc-low cells (losers). Using live tracking of Myc levels, we show that Myc-high ESCs approach the naive pluripotency state, whereas Myc-low ESCs are closer to the differentiation-primed state. In ESC colonies, naive cells eliminate differentiating cells by cell competition, which is determined by a limitation in the time losers are able to survive persistent contact with winners. In the mouse embryo, cell competition promotes pluripotency maintenance by elimination of primed lineages before gastrulation. The mechanism described here is relevant to mammalian embryo development and induced pluripotency.
哺乳动物的上胚层由多能细胞组成,这些细胞能够分化为新个体的所有组织。在上胚层细胞及其体外对应物胚胎干细胞(ESCs)向分化启动的多能性状态发展的过程中,它们会从原始的多能性状态过渡。在这些事件中,上胚层细胞和 ESCs 容易死亡,这是由 Myc 高细胞(胜利者)和 Myc 低细胞(失败者)之间的竞争驱动的。通过对 Myc 水平的实时跟踪,我们发现 Myc 高 ESCs 接近原始多能性状态,而 Myc 低 ESCs 更接近分化启动状态。在 ESC 集落中,通过细胞竞争,原始细胞消除分化细胞,而细胞竞争由失败者在与胜利者持续接触时能够存活的时间限制决定。在小鼠胚胎中,细胞竞争通过在原肠胚形成前消除已启动的谱系来促进多能性维持。这里描述的机制与哺乳动物胚胎发育和诱导多能性有关。