Mature myelin maintenance requires Qki to coactivate PPARβ-RXRα-mediated lipid metabolism

J Clin Invest. 2020 May 1;130(5):2220-2236. doi: 10.1172/JCI131800.

Abstract

Lipid-rich myelin forms electrically insulating, axon-wrapping multilayers that are essential for neural function, and mature myelin is traditionally considered metabolically inert. Surprisingly, we discovered that mature myelin lipids undergo rapid turnover, and quaking (Qki) is a major regulator of myelin lipid homeostasis. Oligodendrocyte-specific Qki depletion, without affecting oligodendrocyte survival, resulted in rapid demyelination, within 1 week, and gradually neurological deficits in adult mice. Myelin lipids, especially the monounsaturated fatty acids and very-long-chain fatty acids, were dramatically reduced by Qki depletion, whereas the major myelin proteins remained intact, and the demyelinating phenotypes of Qki-depleted mice were alleviated by a high-fat diet. Mechanistically, Qki serves as a coactivator of the PPARβ-RXRα complex, which controls the transcription of lipid-metabolism genes, particularly those involved in fatty acid desaturation and elongation. Treatment of Qki-depleted mice with PPARβ/RXR agonists significantly alleviated neurological disability and extended survival durations. Furthermore, a subset of lesions from patients with primary progressive multiple sclerosis were characterized by preferential reductions in myelin lipid contents, activities of various lipid metabolism pathways, and expression level of QKI-5 in human oligodendrocytes. Together, our results demonstrate that continuous lipid synthesis is indispensable for mature myelin maintenance and highlight an underappreciated role of lipid metabolism in demyelinating diseases.

Keywords: Demyelinating disorders; Metabolism; Multiple sclerosis; Neuroscience.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / antagonists & inhibitors
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Demyelinating Diseases / genetics
  • Demyelinating Diseases / metabolism*
  • Demyelinating Diseases / pathology
  • Fatty Acids / genetics
  • Fatty Acids / metabolism
  • Humans
  • Lipid Metabolism*
  • Mice
  • Mice, Knockout
  • Myelin Sheath / genetics
  • Myelin Sheath / metabolism*
  • Myelin Sheath / pathology
  • Oligodendroglia / metabolism
  • Oligodendroglia / pathology
  • PPAR-beta / antagonists & inhibitors
  • PPAR-beta / genetics
  • PPAR-beta / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*

Substances

  • DNA-Binding Proteins
  • Fatty Acids
  • PPAR-beta
  • Qk protein, mouse
  • RNA-Binding Proteins
  • Rxrb protein, mouse