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调控哺乳动物中枢神经系统发育过程中活性依赖型突触修剪的机制。

Mechanisms governing activity-dependent synaptic pruning in the developing mammalian CNS.

机构信息

Department of Neurobiology, Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, MA, USA.

出版信息

Nat Rev Neurosci. 2021 Nov;22(11):657-673. doi: 10.1038/s41583-021-00507-y. Epub 2021 Sep 20.

Abstract

Almost 60 years have passed since the initial discovery by Hubel and Wiesel that changes in neuronal activity can elicit developmental rewiring of the central nervous system (CNS). Over this period, we have gained a more comprehensive picture of how both spontaneous neural activity and sensory experience-induced changes in neuronal activity guide CNS circuit development. Here we review activity-dependent synaptic pruning in the mammalian CNS, which we define as the removal of a subset of synapses, while others are maintained, in response to changes in neural activity in the developing nervous system. We discuss the mounting evidence that immune and cell-death molecules are important mechanistic links by which changes in neural activity guide the pruning of specific synapses, emphasizing the role of glial cells in this process. Finally, we discuss how these developmental pruning programmes may go awry in neurodevelopmental disorders of the human CNS, focusing on autism spectrum disorder and schizophrenia. Together, our aim is to give an overview of how the field of activity-dependent pruning research has evolved, led to exciting new questions and guided the identification of new, therapeutically relevant mechanisms that result in aberrant circuit development in neurodevelopmental disorders.

摘要

自 Hubel 和 Wiesel 最初发现神经元活动的变化可以引发中枢神经系统 (CNS) 的发育性重新布线以来,已经过去了近 60 年。在此期间,我们对自发神经活动和感觉经验诱导的神经元活动变化如何指导中枢神经系统回路发育有了更全面的认识。在这里,我们回顾了哺乳动物中枢神经系统中的活性依赖突触修剪,我们将其定义为在发育中的神经系统中神经活动发生变化时,去除一部分突触,而保留其他突触。我们讨论了越来越多的证据表明,免疫和细胞死亡分子是神经活动变化指导特定突触修剪的重要机制联系,强调了胶质细胞在这个过程中的作用。最后,我们讨论了这些发育性修剪程序在人类中枢神经系统的神经发育障碍中可能出现的异常,重点讨论了自闭症谱系障碍和精神分裂症。总的来说,我们的目的是概述活性依赖修剪研究领域的发展,提出令人兴奋的新问题,并指导鉴定新的、治疗相关的机制,这些机制导致神经发育障碍中异常的回路发育。

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