Research Group Adult Neurogenesis and Neural Stem Cells, Institute of Developmental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Munich-Neuherberg, Germany.
J Neurosci. 2010 Oct 13;30(41):13794-807. doi: 10.1523/JNEUROSCI.1567-10.2010.
The generation of new neurons from neural stem cells in the adult hippocampal dentate gyrus contributes to learning and mood regulation. To sustain hippocampal neurogenesis throughout life, maintenance of the neural stem cell pool has to be tightly controlled. We found that the Notch/RBPJκ-signaling pathway is highly active in neural stem cells of the adult mouse hippocampus. Conditional inactivation of RBPJκ in neural stem cells in vivo resulted in increased neuronal differentiation of neural stem cells in the adult hippocampus at an early time point and depletion of the Sox2-positive neural stem cell pool and suppression of hippocampal neurogenesis at a later time point. Moreover, RBPJκ-deficient neural stem cells displayed impaired self-renewal in vitro and loss of expression of the transcription factor Sox2. Interestingly, we found that Notch signaling increases Sox2 promoter activity and Sox2 expression in adult neural stem cells. In addition, activated Notch and RBPJκ were highly enriched on the Sox2 promoter in adult hippocampal neural stem cells, thus identifying Sox2 as a direct target of Notch/RBPJκ signaling. Finally, we found that overexpression of Sox2 can rescue the self-renewal defect in RBPJκ-deficient neural stem cells. These results identify RBPJκ-dependent pathways as essential regulators of adult neural stem cell maintenance and suggest that the actions of RBPJκ are, at least in part, mediated by control of Sox2 expression.
成年海马齿状回中的神经干细胞产生新的神经元,有助于学习和情绪调节。为了使海马神经发生在整个生命周期中持续存在,必须严格控制神经干细胞池的维持。我们发现 Notch/RBPJκ 信号通路在成年小鼠海马的神经干细胞中高度活跃。体内条件性敲除神经干细胞中的 RBPJκ 会导致成年海马中的神经干细胞早期神经元分化增加,而 Sox2 阳性神经干细胞池耗竭,并抑制海马神经发生。此外,RBPJκ 缺陷型神经干细胞在体外表现出自我更新受损和转录因子 Sox2 表达丧失。有趣的是,我们发现 Notch 信号在成年神经干细胞中增加 Sox2 启动子活性和 Sox2 表达。此外,激活的 Notch 和 RBPJκ 在成年海马神经干细胞中的 Sox2 启动子上高度富集,从而将 Sox2 鉴定为 Notch/RBPJκ 信号的直接靶标。最后,我们发现 Sox2 的过表达可以挽救 RBPJκ 缺陷型神经干细胞的自我更新缺陷。这些结果表明 RBPJκ 依赖性途径是成年神经干细胞维持的重要调节剂,并表明 RBPJκ 的作用至少部分是通过控制 Sox2 表达来介导的。