Nervous System Development and Homeostasis Laboratory, Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Centre for Developmental Neurobiology, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE1 1UL, UK; MRC Centre for Neurodevelopmental Disorders, King's College London, London SE1 1UL, UK.
Cell Rep. 2018 Feb 13;22(7):1710-1721. doi: 10.1016/j.celrep.2018.01.064.
Cortical networks are composed of excitatory projection neurons and inhibitory interneurons. Finding the right balance between the two is important for controlling overall cortical excitation and network dynamics. However, it is unclear how the correct number of cortical interneurons (CIs) is established in the mammalian forebrain. CIs are generated in excess from basal forebrain progenitors, and their final numbers are adjusted via an intrinsically determined program of apoptosis that takes place during an early postnatal window. Here, we provide evidence that the extent of CI apoptosis during this critical period is plastic and cell-type specific and can be reduced in a cell-autonomous manner by acute increases in neuronal activity. We propose that the physiological state of the emerging neural network controls the activity levels of local CIs to modulate their numbers in a homeostatic manner.
皮质网络由兴奋性投射神经元和抑制性中间神经元组成。在两者之间找到正确的平衡对于控制皮质整体兴奋和网络动力学非常重要。然而,目前尚不清楚哺乳动物前脑中间神经元 (CI) 的正确数量是如何建立的。CI 从基底前脑祖细胞中过量产生,其最终数量通过在早期出生后窗口期间发生的内在确定的凋亡程序进行调整。在这里,我们提供的证据表明,在这个关键时期 CI 凋亡的程度是可塑的和细胞类型特异性的,可以通过急性增加神经元活动以细胞自主的方式减少。我们提出,新兴神经网络的生理状态控制局部 CI 的活动水平,以使其数量以稳态方式进行调节。