皮层发育过程中神经元间凋亡的稳态调节。

Journal of Experimental Neuroscience Pub Date : 2018-07-05 eCollection Date: 2018-01-01 DOI:10.1177/1179069518784277
Myrto Denaxa, Guilherme Neves, Juan Burrone, Vassilis Pachnis
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引用次数: 9

摘要

哺乳动物皮层由两种主要的神经元类型组成:主要兴奋性锥体神经元(PNs)和抑制性中间神经元(INs)。这两个神经元群之间的相互作用——分别驱动兴奋和抑制(E/I平衡)——对控制大脑的整体活动至关重要。许多神经和精神疾病与E/I平衡的变化有关。因此,神经网络采用几种不同的机制将其放电速率维持在一个稳定的水平,这并不奇怪,这些机制统称为稳态可塑性形式。在这里,我们分享了我们的观点,即IN种群的大小如何为控制大脑活动提供早期稳态检查点。在最近发表在Cell Reports上的一篇论文中,我们证明了在关键的产后早期,细胞凋亡的程度是可塑的,细胞类型特异性的,并且可以通过神经元活动的急性增加以细胞自主的方式减少。我们提出,网络的生理状态与其细胞单位之间的关键相互作用微调了IN种群的大小,目的是稳定网络活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Homeostatic Regulation of Interneuron Apoptosis During Cortical Development.

Homeostatic Regulation of Interneuron Apoptosis During Cortical Development.

Homeostatic Regulation of Interneuron Apoptosis During Cortical Development.

The mammalian cortex consists of two main neuronal types: the principal excitatory pyramidal neurons (PNs) and the inhibitory interneurons (INs). The interplay between these two neuronal populations - which drive excitation and inhibition (E/I balance), respectively - is crucial for controlling the overall activity in the brain. A number of neurological and psychiatric disorders have been associated with changes in E/I balance. It is not surprising, therefore, that neural networks employ several different mechanisms to maintain their firing rates at a stable level, collectively referred as homeostatic forms of plasticity. Here, we share our views on how the size of IN populations may provide an early homeostatic checkpoint for controlling brain activity. In a recent paper published in Cell Reports, we demonstrate that the extent of IN apoptosis during a critical early postnatal period is plastic, cell type specific, and can be reduced in a cell-autonomous manner by acute increases in neuronal activity. We propose that a critical interplay between the physiological state of the network and its cellular units fine-tunes the size of IN populations with the aim of stabilizing network activity.

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