Bergles Dwight E, Richardson William D
The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, WBSB 1001, Baltimore, Maryland 21205.
Wolfson Institute for Biomedical Research, University College London, London WC1E 6BT, United Kingdom.
Cold Spring Harb Perspect Biol. 2015 Aug 20;8(2):a020453. doi: 10.1101/cshperspect.a020453.
Oligodendrocyte precursor cells (OPCs) originate in the ventricular zones (VZs) of the brain and spinal cord and migrate throughout the developing central nervous system (CNS) before differentiating into myelinating oligodendrocytes (OLs). It is not known whether OPCs or OLs from different parts of the VZ are functionally distinct. OPCs persist in the postnatal CNS, where they continue to divide and generate myelinating OLs at a decreasing rate throughout adult life in rodents. Adult OPCs respond to injury or disease by accelerating their cell cycle and increasing production of OLs to replace lost myelin. They also form synapses with unmyelinated axons and respond to electrical activity in those axons by generating more OLs and myelin locally. This experience-dependent "adaptive" myelination is important in some forms of plasticity and learning, for example, motor learning. We review the control of OL lineage development, including OL population dynamics and adaptive myelination in the adult CNS.
少突胶质前体细胞(OPCs)起源于脑和脊髓的脑室区(VZs),并在整个发育中的中枢神经系统(CNS)中迁移,然后分化为髓鞘形成少突胶质细胞(OLs)。目前尚不清楚来自脑室区不同部位的OPCs或OLs在功能上是否存在差异。OPCs在出生后的中枢神经系统中持续存在,在啮齿动物的整个成年期,它们继续分裂并以逐渐降低的速率产生髓鞘形成OLs。成年OPCs通过加速其细胞周期和增加OLs的产生来替代丢失的髓鞘,从而对损伤或疾病作出反应。它们还与无髓鞘轴突形成突触,并通过在局部产生更多的OLs和髓鞘来响应这些轴突中的电活动。这种依赖经验的“适应性”髓鞘形成在某些形式的可塑性和学习(例如运动学习)中很重要。我们综述了OL谱系发育的调控,包括成年中枢神经系统中的OL群体动态和适应性髓鞘形成。