Wang S, Young K M
Menzies Research Institute Tasmania, University of Tasmania, Hobart 7000, Australia.
Menzies Research Institute Tasmania, University of Tasmania, Hobart 7000, Australia.
Neuroscience. 2014 Sep 12;276:148-60. doi: 10.1016/j.neuroscience.2013.10.018. Epub 2013 Oct 23.
CNS white matter is subject to a novel form of neural plasticity which has been termed "myelin plasticity". It is well established that oligodendrocyte generation and the addition of new myelin internodes continue throughout normal adulthood. These new myelin internodes maybe required for the de novo myelination of previously unmyelinated axons, myelin sheath replacement, or even myelin remodeling. Each process could alter axonal conduction velocity, but to what end? We review the changes that occur within the white matter over the lifetime, the known regulators and mediators of white matter plasticity in the mature CNS, and the physiological role this plasticity may play in CNS function.
中枢神经系统白质存在一种新型神经可塑性,被称为“髓鞘可塑性”。众所周知,少突胶质细胞的生成以及新髓鞘节段的添加在成年期正常阶段持续存在。这些新的髓鞘节段可能是先前无髓鞘轴突进行新生髓鞘形成、髓鞘鞘膜替换甚至髓鞘重塑所必需的。每个过程都可能改变轴突传导速度,但目的是什么呢?我们综述了一生中白质内发生的变化、成熟中枢神经系统中已知的白质可塑性调节因子和介质,以及这种可塑性可能在中枢神经系统功能中发挥的生理作用。