Centre for Integrative Physiology, School of Biomedical Sciences, University of Edinburgh, Edinburgh, United Kingdom.
PLoS One. 2012;7(8):e42572. doi: 10.1371/journal.pone.0042572. Epub 2012 Aug 3.
Development of the cerebellum proceeds under the precise spatio-temporal control of several key developmental signalling pathways, including the Wnt/β-catenin pathway. We recently reported the activity of Wnt/β-catenin signalling in the perinatal cerebellar ventricular zone (VZ), a germinal centre in the developing cerebellum that gives rise to GABAergic and glial cells. In order to investigate the normal function of Wnt/β-catenin signalling in the VZ and the cell lineages it gives rise to, we used a combination of ex vivo cerebellar slice culture and in vivo genetic manipulation to dysregulate its activity during late embryonic development. Activation of the pathway at the cerebellar ventricular zone led to a reduction in the number of cells expressing the glial lineage markers Sox9 and GFAP and the interneuron marker Pax2, but had no consistent effect on either proliferation or apoptosis. Our findings suggest that activation of the Wnt/β-catenin pathway in the cerebellar ventricular zone causes a shift in the cell types produced, most likely due to disruption of normal differentiation. Thus, we propose that regulation of Wnt/β-catenin signalling levels are required for normal development of cells arising from the cerebellar ventricular zone during late embryogenesis.
小脑的发育是在几个关键的发育信号通路的精确时空控制下进行的,包括 Wnt/β-catenin 通路。我们最近报道了 Wnt/β-catenin 信号在围产期小脑脑室区(VZ)的活性,VZ 是发育中小脑的生发中心,产生 GABA 能和神经胶质细胞。为了研究 Wnt/β-catenin 信号在 VZ 及其产生的细胞谱系中的正常功能,我们使用了体外小脑切片培养和体内遗传操作的组合,在胚胎晚期发育过程中失调其活性。在小脑脑室区激活该通路导致表达神经胶质谱系标志物 Sox9 和 GFAP 以及中间神经元标志物 Pax2 的细胞数量减少,但对增殖或凋亡没有一致的影响。我们的研究结果表明,小脑脑室区 Wnt/β-catenin 通路的激活导致产生的细胞类型发生转变,这很可能是由于正常分化的中断。因此,我们提出,在胚胎晚期,调节 Wnt/β-catenin 信号水平对于源自小脑脑室区的细胞的正常发育是必需的。