Humięcka Monika, Szpila Marcin, Kłoś Piotr, Maleszewski Marek, Szczepańska Katarzyna
Department of Embryology, Faculty of Biology, Institute of Zoology, University of Warsaw, Warsaw, Poland.
PLoS One. 2017 Mar 31;12(3):e0175032. doi: 10.1371/journal.pone.0175032. eCollection 2017.
The mouse preimplantation embryo generates the precursors of trophectoderm (TE) and inner cell mass (ICM) during the 8- to 16-cell stage transition, when the apico-basal polarized blastomeres undergo divisions that give rise to cells with different fate. Asymmetric segregation of polar domain at 8-16 cell division generate two cell types, polar cells which adopt an outer position and develop in TE and apolar cells which are allocated to inner position as the precursors of ICM. It is still not know when the blastomeres of 8-cell stage start to be determined to undergo asymmetric division. Here, we analyze the frequency of symmetric and asymmetric divisions of blastomeres isolated from 8-cell stage embryo before and after compaction. Using p-Ezrin as the polarity marker we found that size of blastomeres in 2/16 pairs cannot be used as a criterion for distinguishing symmetric and asymmetric divisions. Our results showed that at early 8-cell stage, before any visible signs of cortical polarity, a subset of blastomeres had been already predestined to divide asymmetrically. We also showed that almost all of 8-cell stage blastomeres isolated from compacted embryo divide asymmetrically, whereas in intact embryos, the frequency of asymmetric divisions is significantly lower. Therefore we conclude that in intact embryo the frequency of symmetric and asymmetric division is regulated by cell-cell interactions.
小鼠植入前胚胎在8细胞至16细胞阶段转变过程中产生滋养外胚层(TE)和内细胞团(ICM)的前体,此时顶-基极化的卵裂球进行分裂,产生具有不同命运的细胞。8至16细胞分裂时极性结构域的不对称分离产生两种细胞类型,即处于外部位置并发育为TE的极性细胞和作为ICM前体被分配到内部位置的非极性细胞。目前仍不清楚8细胞期的卵裂球何时开始被确定进行不对称分裂。在此,我们分析了致密化前后从8细胞期胚胎分离的卵裂球对称和不对称分裂的频率。使用磷酸化埃兹蛋白作为极性标记,我们发现16对中的2对卵裂球大小不能用作区分对称和不对称分裂的标准。我们的结果表明,在8细胞早期,在任何可见的皮质极性迹象出现之前,一部分卵裂球已经注定要进行不对称分裂。我们还表明,从致密化胚胎分离的几乎所有8细胞期卵裂球都进行不对称分裂,而在完整胚胎中,不对称分裂的频率显著较低。因此我们得出结论,在完整胚胎中,对称和不对称分裂的频率受细胞间相互作用的调节。