Developmental Biology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10065, USA
Neuroscience Graduate Program, Weill Cornell Medical College, 1300 York Avenue, New York, NY 10065, USA.
Development. 2020 Mar 11;147(5):dev184150. doi: 10.1242/dev.184150.
Orderly division of radial glial progenitors (RGPs) in the developing mammalian cerebral cortex generates deep and superficial layer neurons progressively. However, the mechanisms that control RGP behavior and precise neuronal output remain elusive. Here, we show that the oxidative stress level progressively increases in the developing mouse cortex and regulates RGP behavior and neurogenesis. As development proceeds, numerous gene pathways linked to reactive oxygen species (ROS) and oxidative stress exhibit drastic changes in RGPs. Selective removal of PRDM16, a transcriptional regulator highly expressed in RGPs, elevates ROS level and induces expression of oxidative stress-responsive genes. Coinciding with an enhanced level of oxidative stress, RGP behavior was altered, leading to abnormal deep and superficial layer neuron generation. Simultaneous expression of mitochondrially targeted catalase to reduce cellular ROS levels significantly suppresses cortical defects caused by PRDM16 removal. Together, these findings suggest that oxidative stress actively regulates RGP behavior to ensure proper neurogenesis in the mammalian cortex.
在哺乳动物大脑皮层的发育过程中,放射状胶质前体细胞(RGPs)有序分裂,逐渐产生深层和浅层神经元。然而,控制 RGPs 行为和精确神经元输出的机制仍不清楚。在这里,我们发现发育中的小鼠皮层中的氧化应激水平逐渐升高,并调节 RGPs 的行为和神经发生。随着发育的进行,与活性氧(ROS)和氧化应激相关的许多基因途径在 RGPs 中发生剧烈变化。选择性去除 PRDM16,一种在 RGPs 中高度表达的转录调节剂,会升高 ROS 水平并诱导氧化应激反应基因的表达。与氧化应激水平的升高相吻合,RGPs 的行为发生改变,导致深层和浅层神经元生成异常。同时表达靶向线粒体的过氧化氢酶以降低细胞内 ROS 水平,可显著抑制 PRDM16 缺失引起的皮质缺陷。总之,这些发现表明氧化应激积极调节 RGPs 的行为,以确保哺乳动物皮层中适当的神经发生。