Kadoya Minori, Sasai Noriaki
Developmental Biomedical Science, Graduate School of Biological Sciences, Nara Institute of Science and Technology, Ikoma, Japan.
Front Neurosci. 2019 Sep 25;13:1022. doi: 10.3389/fnins.2019.01022. eCollection 2019.
The neural tube is composed of a number of neural progenitors and postmitotic neurons distributed in a quantitatively and spatially precise manner. The floor plate, located in the ventral-most region of the neural tube, has a lot of unique characteristics, including a low cell proliferation rate. The mechanisms by which this region-specific proliferation rate is regulated remain elusive. Here we show that the activity of the mTOR signaling pathway, which regulates the proliferation of the neural progenitor cells, is significantly lower in the floor plate than in other domains of the embryonic neural tube. We identified the forkhead-type transcription factor FoxA2 as a negative regulator of mTOR signaling in the floor plate, and showed that FoxA2 transcriptionally induces the expression of the E3 ubiquitin ligase RNF152, which together with its substrate RagA, regulates cell proliferation via the mTOR pathway. Silencing of RNF152 led to the aberrant upregulation of the mTOR signal and aberrant cell division in the floor plate. Taken together, the present findings suggest that floor plate cell number is controlled by the negative regulation of mTOR signaling through the activity of FoxA2 and its downstream effector RNF152.
神经管由许多神经祖细胞和有丝分裂后的神经元组成,它们以定量和空间精确的方式分布。位于神经管最腹侧区域的底板具有许多独特的特征,包括低细胞增殖率。调节该区域特异性增殖率的机制仍然不清楚。在这里,我们表明,调节神经祖细胞增殖的mTOR信号通路的活性在底板中显著低于胚胎神经管的其他区域。我们确定叉头型转录因子FoxA2是底板中mTOR信号的负调节因子,并表明FoxA2转录诱导E3泛素连接酶RNF152的表达,RNF152与其底物RagA一起通过mTOR途径调节细胞增殖。RNF152的沉默导致底板中mTOR信号的异常上调和细胞分裂异常。综上所述,目前的研究结果表明,底板细胞数量是通过FoxA2及其下游效应物RNF152的活性对mTOR信号的负调节来控制的。