Yasugi Tetsuo, Nishimura Takashi
Laboratory for Growth Control Signaling, RIKEN Center for Developmental Biology (CDB), 2-2-3 Minatojima-Minamimachi, Chuo-ku, Kobe, Hyogo 650-0047, Japan.
Dev Growth Differ. 2016 Jan;58(1):73-87. doi: 10.1111/dgd.12245. Epub 2015 Dec 21.
For the construction of complex neural networks, the generation of neurons and glia must be tightly regulated both spatially and temporally. One of the major issues in neural development is the generation of a large variety of neurons and glia over time from a relatively small number of neural stem cells. In Drosophila, neural stem cells, called neuroblasts (NBs), have been used as a useful model system to uncover the molecular and cellular machinery involved in the establishment of neural diversity. NBs divide asymmetrically and produce another self-renewing progenitor cell and a differentiating cell. NBs are subdivided into several types based on their location in the central nervous system. Each type of NB has specific features related to the timing of cell generation, cell cycle progression, temporal patterning for neuronal specification, and termination mechanism. In this review, we focus on the molecular mechanisms that regulate the proliferation of NBs and generate a large variety of neuronal and glia subtypes during development.
对于复杂神经网络的构建,神经元和神经胶质细胞的生成必须在空间和时间上受到严格调控。神经发育中的一个主要问题是,随着时间的推移,相对少量的神经干细胞如何产生大量不同类型的神经元和神经胶质细胞。在果蝇中,神经干细胞被称为神经母细胞(NBs),它已成为一个有用的模型系统,用于揭示参与建立神经多样性的分子和细胞机制。神经母细胞进行不对称分裂,产生另一个自我更新的祖细胞和一个分化细胞。根据神经母细胞在中枢神经系统中的位置,可将其细分为几种类型。每种类型的神经母细胞都具有与细胞生成时间、细胞周期进程、神经元特化的时间模式以及终止机制相关的特定特征。在这篇综述中,我们重点关注在发育过程中调节神经母细胞增殖并产生大量不同神经元和神经胶质细胞亚型的分子机制。