Faculty of Life Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
Reproduction. 2013 Mar 1;145(3):R65-80. doi: 10.1530/REP-12-0381.
During mammalian preimplantation development, the fertilised egg gives rise to a group of pluripotent embryonic cells, the epiblast, and to the extraembryonic lineages that support the development of the foetus during subsequent phases of development. This preimplantation period not only accommodates the first cell fate decisions in a mammal's life but also the transition from a totipotent cell, the zygote, capable of producing any cell type in the animal, to cells with a restricted developmental potential. The cellular and molecular mechanisms governing the balance between developmental potential and lineage specification have intrigued developmental biologists for decades. The preimplantation mouse embryo offers an invaluable system to study cell differentiation as well as the emergence and maintenance of pluripotency in the embryo. Here we review the most recent findings on the mechanisms controlling these early cell fate decisions. The model that emerges from the current evidence indicates that cell differentiation in the preimplantation embryo depends on cellular interaction and intercellular communication. This strategy underlies the plasticity of the early mouse embryo and ensures the correct specification of the first mammalian cell lineages.
在哺乳动物胚胎着床前发育过程中,受精卵产生一组多能胚胎细胞,即外胚层,以及支持胚胎在随后发育阶段发育的胚胎外谱系。这个胚胎着床前时期不仅适应了哺乳动物生命中的第一个细胞命运决定,也适应了从全能细胞(受精卵)向具有有限发育潜力的细胞的转变。几十年来,控制发育潜能和谱系特化之间平衡的细胞和分子机制一直令发育生物学家着迷。胚胎着床前的小鼠胚胎为研究细胞分化以及胚胎中多能性的出现和维持提供了一个非常有价值的系统。在这里,我们回顾了控制这些早期细胞命运决定的最新发现。从目前的证据中得出的模型表明,胚胎着床前胚胎中的细胞分化取决于细胞间的相互作用和细胞间的通讯。这种策略是早期小鼠胚胎可塑性的基础,并确保了第一个哺乳动物谱系的正确特化。