Fractalkine signaling regulates oligodendroglial cell genesis from SVZ precursor cells

Stem Cell Reports. 2021 Aug 10;16(8):1968-1984. doi: 10.1016/j.stemcr.2021.06.010. Epub 2021 Jul 15.

Abstract

Neural and oligodendrocyte precursor cells (NPCs and OPCs) in the subventricular zone (SVZ) of the brain contribute to oligodendrogenesis throughout life, in part due to direct regulation by chemokines. The role of the chemokine fractalkine is well established in microglia; however, the effect of fractalkine on SVZ precursor cells is unknown. We show that murine SVZ NPCs and OPCs express the fractalkine receptor (CX3CR1) and bind fractalkine. Exogenous fractalkine directly enhances OPC and oligodendrocyte genesis from SVZ NPCs in vitro. Infusion of fractalkine into the lateral ventricle of adult NPC lineage-tracing mice leads to increased newborn OPC and oligodendrocyte formation in vivo. We also show that OPCs secrete fractalkine and that inhibition of endogenous fractalkine signaling reduces oligodendrocyte formation in vitro. Finally, we show that fractalkine signaling regulates oligodendrogenesis in cerebellar slices ex vivo. In summary, we demonstrate a novel role for fractalkine signaling in regulating oligodendrocyte genesis from postnatal CNS precursor cells.

Keywords: CX3CR1; OPC; Regeneration; SVZ; chemokine; fractalkine; myelin; neural stem cell; oligodendrocyte; oligodendrocyte precursor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CX3C Chemokine Receptor 1 / genetics
  • CX3C Chemokine Receptor 1 / metabolism*
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cells, Cultured
  • Chemokine CX3CL1 / metabolism*
  • Chemokine CX3CL1 / pharmacology
  • Gene Expression / drug effects
  • Lateral Ventricles / cytology
  • Lateral Ventricles / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Microscopy, Confocal
  • Oligodendrocyte Precursor Cells / cytology
  • Oligodendrocyte Precursor Cells / metabolism*
  • Oligodendrocyte Transcription Factor 2 / genetics
  • Oligodendrocyte Transcription Factor 2 / metabolism
  • Oligodendroglia / cytology
  • Oligodendroglia / metabolism*
  • SOXB1 Transcription Factors / genetics
  • SOXB1 Transcription Factors / metabolism
  • Signal Transduction*

Substances

  • CX3C Chemokine Receptor 1
  • Chemokine CX3CL1
  • Oligodendrocyte Transcription Factor 2
  • SOXB1 Transcription Factors
  • Sox2 protein, mouse

Grants and funding