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Cellular and molecular control of neurogenesis in the mammalian telencephalon.

机译:哺乳动物端脑神经发生的细胞和分子控制。

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The mammalian telencephalon exhibits an amazing diversity of neuronal types. The generation of this diversity relies on multiple developmental strategies, including the regional patterning of progenitors, their temporal specification, and the generation of intermediate progenitor populations. Progress has recently been made in characterizing some of the mechanisms involved. In particular, intermediate progenitors have been shown to play important roles in the generation of neurons in the cerebral cortex, and the properties and lineage relationships between radial glial cells and these intermediate progenitors have recently been examined by elegant time-lapse microscopic studies. Multiple pathways control the progression of neural lineages from multipotent stem cells to intermediate progenitors, postmitotic precursors and finally mature neurons. The regulation of two essential steps, neuronal commitment and specification of subtype identities, is increasingly well understood. These two steps are clearlydistinct but co-ordinately regulated by common transcription factors such as neurogenins and Pax6. As our knowledge of the mechanisms of subtype specification of telencephalic neurons progresses, it will become possible to direct stem cells into generating particular telencephalic neuronal populations, opening the way to efficient neuronal replacement therapies.
机译:哺乳动物的端脑表现出惊人的神经元类型多样性。这种多样性的产生取决于多种发展策略,包括祖细胞的区域模式,它们的时间规格以及中间祖细胞的产生。最近在表征某些涉及的机制方面取得了进展。特别是,中间祖细胞已显示在大脑皮层神经元的产生中起重要作用,最近通过优雅的延时显微镜研究对lapse神经胶质细胞与这些中间祖细胞之间的特性和谱系关系进行了研究。多种途径控制着神经谱系从多能干细胞到中间祖细胞,有丝分裂后的前体以及最终成熟的神经元的进程。对两个基本步骤的调节,即神经元承诺和亚型身份的指定,已越来越为人所理解。这两个步骤明显不同,但由常见的转录因子(例如神经生成素和Pax6)进行协调调节。随着我们对端脑神经元亚型规范机制的了解的发展,将可能指导干细胞生成特定的端脑神经元种群,从而为有效的神经元替代疗法开辟了道路。

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