Department of Applied Biological Science, Graduate School of Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda-shi, Chiba, 278-8510, Japan.
Research Institute for Science and Technology, Tokyo University of Science, 2641 Yamazaki, Noda-shi, Chiba, 278-8510, Japan.
Dev Genes Evol. 2019 May;229(2-3):73-81. doi: 10.1007/s00427-018-00625-1. Epub 2019 Jan 10.
Establishment of the body plan of multicellular organisms by the primary body axis determination and cell-fate specification is a key issue in biology. We have examined the mRNA localization of three Wnt pathway components gsk3β, β-catenin, and disheveled and investigated the effects of four selective inhibitors of these proteins on the early developmental stages of the spiral cleavage embryo of the fresh water snail Lymnaea (L.) stagnalis. mRNAs for gsk3β and β-catenin were distributed uniformly throughout the embryo during development whereas disheveled mRNA showed specific localization with intra- and inter-blastomere differences in concentration along the A-V axis during spiral cleavages. Remarkably, through inhibitor studies, we identified a short sensitive period from the 2- to 4-cell stage in which GSK3β inhibition by the highly specific 1-azakenpaullone (AZ) and by LiCl induced a subsequent dramatic developmental delay and alteration of the cleavage patterns of blastomeres at the fifth cleavage (16- to 24-cell stage) resulting in exogastrulation and other abnormalities in later stages. Inhibition of β-Catenin or Disheveled had no effect. Our inhibitor experiments establish a novel role for GSK3β in the developmental timing and orientated cell division of the snail embryo. Further work will be needed to identify the downstream targets of the kinase.
多细胞生物的体轴建立和细胞命运决定是生物学的关键问题。我们研究了 Wnt 信号通路的三个成分 gsk3β、β-catenin 和 disheveled 的 mRNA 定位,并调查了这四种蛋白选择性抑制剂对淡水螺(Lymnaea (L.) stagnalis)螺旋分裂胚胎早期发育阶段的影响。在胚胎发育过程中,gs k3β和 β-catenin 的 mRNA 均匀分布在整个胚胎中,而 disheveled 的 mRNA 则沿 A-V 轴在细胞内和细胞间表现出特异性定位,浓度存在差异。值得注意的是,通过抑制剂研究,我们确定了一个从 2-细胞到 4-细胞的短暂敏感时期,在此期间,高特异性的 1-azakenpaullone(AZ)和 LiCl 对 GSK3β的抑制导致随后的发育延迟和第五次分裂(16-至 24-细胞阶段)时的分裂模式发生改变,导致胚胎外胚和后期的其他异常。抑制 β-catenin 或 disheveled 则没有效果。我们的抑制剂实验为 GSK3β在蜗牛胚胎的发育时间和定向细胞分裂中确立了新的作用。进一步的工作将需要确定激酶的下游靶标。