Prefrontal cortex NG2 glia undergo a developmental switch in their responsiveness to exercise

Dev Neurobiol. 2018 Jul;78(7):687-700. doi: 10.1002/dneu.22590. Epub 2018 Mar 31.

Abstract

Aerobic exercise is known to influence brain function, e.g., enhancing executive function in both children and adults, with many of these influences being attributed to alterations in neurogenesis and neuronal function. Yet oligodendroglia in adult brains have also been reported to be highly responsive to exercise, including in the prefrontal cortex (PFC), a late myelinating region implicated in working memory. However, whether exercise affects oligodendroglia or myelination in juveniles, either in the PFC or in other brain regions, remains unknown. To address this, both juvenile and young adult mice were provided free access to running wheels for four weeks followed by an analysis of oligodendrocyte development and myelination in the PFC and the corpus callosum, a major white matter tract. Working memory and PFC NG2+ cell development were both affected by exercise in juvenile mice, yet surprisingly these exercise-mediated effects were distinct in juveniles and young adults. In the PFC, NG2+ cell proliferation was increased in exercising juveniles, but not young adults, whereas newly-born oligodendrocyte production was increased in exercising young adults, but not juveniles. Although no overall changes in myelin genes were found, elevated levels of Monocarboxylate Transporter 1, a glial lactate transporter important during active myelination, were found in the PFC of exercising young adults. Overall our findings reveal that long-term exercise modulates PFC glial development and does so differentially in juvenile and young adult mice, providing insight into the cellular responses that may underlie cognitive benefits to teenagers and young adults in response to exercise. © 2018 Wiley Periodicals, Inc. Develop Neurobiol 78: 687-700, 2018.

Keywords: MCT1; NG2 glia; exercise; myelin; oligodendrocyte; prefrontal cortex.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Antigens / metabolism*
  • Cell Proliferation / physiology
  • Female
  • Maze Learning / physiology
  • Mice, Inbred C57BL
  • Monocarboxylic Acid Transporters / metabolism
  • Oligodendroglia / cytology
  • Oligodendroglia / metabolism*
  • Prefrontal Cortex / cytology
  • Prefrontal Cortex / growth & development*
  • Prefrontal Cortex / metabolism*
  • Proteoglycans / metabolism*
  • Running / physiology*
  • Running / psychology
  • Symporters / metabolism

Substances

  • Antigens
  • Monocarboxylic Acid Transporters
  • Proteoglycans
  • Symporters
  • chondroitin sulfate proteoglycan 4
  • monocarboxylate transport protein 1