Mechanistic insights into the role of mTOR signaling in neuronal differentiation.

Neurogenesis (Austin, Tex.) Pub Date : 2015-11-13 eCollection Date: 2015-01-01 DOI:10.1080/23262133.2015.1058684
Joseph M Bateman
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引用次数: 11

Abstract

Temporal control of neuronal differentiation is critical to produce a complete and fully functional nervous system. Loss of the precise temporal control of neuronal cell fate can lead to defects in cognitive development and to disorders such as epilepsy and autism. Mechanistic target of rapamycin (mTOR) is a large serine/threonine kinase that acts as a crucial sensor of cellular homeostasis. mTOR signaling has recently emerged as a key regulator of neurogenesis. However, the mechanism by which mTOR regulates neurogenesis is poorly understood. In constrast to other functions of the pathway, 'neurogenic mTOR pathway factors' have not previously been identified. We have very recently used Drosophila as a model system to identify the gene unkempt as the first component of the mTOR pathway regulating neuronal differentiation. Our study demonstrates that specific adaptor proteins exist that channel mTOR signaling toward the regulation of neuronal cell fate. In this Commentary we discuss the role of mTOR signaling in neurogenesis and the significance of these findings in advancing our understanding of the mechanism by which mTOR signaling controls neuronal differentiation.

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mTOR信号在神经元分化中的作用机制。
神经元分化的时间控制是产生一个完整和功能齐全的神经系统的关键。失去对神经元细胞命运的精确时间控制可能导致认知发育缺陷和癫痫和自闭症等疾病。雷帕霉素的机制靶点(mTOR)是一种大型丝氨酸/苏氨酸激酶,作为细胞稳态的关键传感器。mTOR信号最近被认为是神经发生的关键调节因子。然而,mTOR调控神经发生的机制尚不清楚。与该通路的其他功能相比,“神经源性mTOR通路因子”此前尚未被确定。我们最近使用果蝇作为模型系统来确定基因unkempt是调节神经元分化的mTOR通路的第一个组成部分。我们的研究表明,存在特定的衔接蛋白,将mTOR信号传导到神经元细胞命运的调节中。在这篇评论中,我们讨论了mTOR信号在神经发生中的作用,以及这些发现在促进我们对mTOR信号控制神经元分化机制的理解方面的意义。
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