Wellcome Trust - Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, Cambridge CB2 1QR, United Kingdom; email:
Department of Veterinary Medicine, University of Cambridge, Cambridge CB3 0ES, United Kingdom.
Annu Rev Neurosci. 2018 Jul 8;41:139-161. doi: 10.1146/annurev-neuro-072116-031054. Epub 2018 Apr 4.
The addition of new neurons and oligodendroglia in the postnatal and adult mammalian brain presents distinct forms of gray and white matter plasticity. Substantial effort has been devoted to understanding the cellular and molecular mechanisms controlling postnatal neurogenesis and gliogenesis, revealing important parallels to principles governing the embryonic stages. While during central nervous system development, scripted temporal and spatial patterns of neural and glial progenitor proliferation and differentiation are necessary to create the nervous system architecture, it remains unclear what driving forces maintain and sustain postnatal neural stem cell (NSC) and oligodendrocyte progenitor cell (OPC) production of new neurons and glia. In recent years, neuronal activity has been identified as an important modulator of these processes. Using the distinct properties of neurotransmitter ionotropic and metabotropic channels to signal downstream cellular events, NSCs and OPCs share common features in their readout of neuronal activity patterns. Here we review the current evidence for neuronal activity-dependent control of NSC/OPC proliferation and differentiation in the postnatal brain, highlight some potential mechanisms used by the two progenitor populations, and discuss future studies that might advance these research areas further.
在出生后和成年哺乳动物的大脑中,新神经元和少突胶质细胞的增加呈现出明显的灰质和白质可塑性形式。人们已经投入了大量的精力来理解控制出生后神经发生和神经胶质发生的细胞和分子机制,揭示了与控制胚胎阶段的原则的重要相似之处。虽然在中枢神经系统发育过程中,神经和神经胶质前体细胞增殖和分化的预定的时空模式对于创建神经系统结构是必要的,但尚不清楚是什么驱动力维持和维持出生后神经干细胞(NSC)和少突胶质祖细胞(OPC)产生新的神经元和神经胶质。近年来,神经元活动已被确定为这些过程的重要调节剂。利用神经递质离子型和代谢型通道的独特特性来传递下游细胞事件的信号,NSC 和 OPC 在其对神经元活动模式的解读中具有共同的特征。在这里,我们回顾了目前关于神经元活动依赖性控制出生后大脑中 NSC/OPC 增殖和分化的证据,强调了两个祖细胞群体使用的一些潜在机制,并讨论了可能进一步推进这些研究领域的未来研究。