Oligodendrocyte Development and Plasticity

  1. William D. Richardson2
  1. 1The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University, WBSB 1001, Baltimore, Maryland 21205
  2. 2Wolfson Institute for Biomedical Research, University College London, London WC1E 6BT, United Kingdom
  1. Correspondence: dbergles{at}jhmi.edu; w.richardson{at}ucl.ac.uk

Abstract

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.



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      1. Cold Spring Harb. Perspect. Biol. 8: a020453 Copyright © 2016 Cold Spring Harbor Laboratory Press; all rights reserved

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