Laboratory of Cell Biology, Department of Bioinformatics, Graduate School of Engineering, Soka University, 1-236 Tangi-machi, Hachioji, Tokyo, 192-8577, Japan.
Department of Advanced Clinical Glycobiology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Kita 15, Nishi 7, Kita-ku, Sapporo, Hokkaido, 060-8638, Japan.
Sci Rep. 2021 Jan 14;11(1):1276. doi: 10.1038/s41598-020-79666-4.
Embryonic stem cells (ESCs) and epiblast-like cells (EpiLCs) recapitulate in vitro the epiblast first cell lineage decision, allowing characterization of the molecular mechanisms underlying pluripotent state transition. Here, we performed a comprehensive and comparative analysis of total glycomes of mouse ESCs and EpiLCs, revealing that overall glycosylation undergoes dramatic changes from early stages of development. Remarkably, we showed for the first time the presence of a developmentally regulated network orchestrating glycosylation changes and identified polycomb repressive complex 2 (PRC2) as a key component involved in this process. Collectively, our findings provide novel insights into the naïve-to-primed pluripotent state transition and advance the understanding of glycosylation complex regulation during early mouse embryonic development.
胚胎干细胞(ESCs)和类胚层细胞(EpiLCs)在体外再现了胚层的第一个细胞谱系决定,从而能够对多能性状态转变的分子机制进行特征描述。在这里,我们对小鼠 ESCs 和 EpiLCs 的总糖组进行了全面和比较分析,结果表明,整体糖基化在发育的早期阶段发生了巨大变化。值得注意的是,我们首次展示了一个协调糖基化变化的发育调控网络的存在,并确定多梳抑制复合物 2(PRC2)是该过程中的关键组成部分。总的来说,我们的研究结果为幼稚到原始多能性状态转变提供了新的见解,并推进了对早期小鼠胚胎发育过程中糖基化复合物调控的理解。