Demyelination Produces a Shift in the Population of Cortical Neurons That Synapse with Callosal Oligodendrocyte Progenitor Cells

eNeuro. 2025 Jun 12;12(6):ENEURO.0113-25.2025. doi: 10.1523/ENEURO.0113-25.2025. Print 2025 Jun.

Abstract

Oligodendrocyte progenitor cells (OPCs) receive synaptic input from a diverse range of neurons in the developing and adult brain. Understanding whether the neuronal populations that synapse with OPCs in the healthy brain is altered by demyelination and/or remyelination may support the advancement of neuroprotective or myelin repair strategies being developed for demyelinating diseases such as multiple sclerosis. To explore this possibility, we employed cre-lox transgenic technology to facilitate the infection of OPCs by a modified rabies virus, enabling the retrograde monosynaptic tracing of neuron→OPC connectivity. In the healthy adult mouse, OPCs in the corpus callosum primarily received synaptic input from ipsilateral cortical neurons. Of the cortical neurons, ∼50% were layer V pyramidal cells. Cuprizone demyelination reduced the total number of labeled neurons. However, the frequency/kinetics of mini-excitatory postsynaptic currents recorded from OPCs appeared preserved. Of particular interest, demyelination increased the number of labeled layer II/III pyramidal neurons and also increased at the expense of layer V pyramidal neurons, a change that was largely ameliorated by remyelination. These data suggest that in the healthy adult mouse brain, callosal OPCs primarily receive synaptic input from cortical layer V pyramidal neurons. However, callosal demyelination is associated with a population switch and OPCs equally synapse with layer II/III and V pyramidal neurons to synapse with OPCs, until myelin is restored.

Keywords: NG2 glia; demyelination; oligodendrocyte progenitor cells; rabies virus; remyelination; synapse.

MeSH terms

  • Animals
  • Cerebral Cortex* / pathology
  • Cerebral Cortex* / physiopathology
  • Corpus Callosum* / pathology
  • Corpus Callosum* / physiopathology
  • Cuprizone / toxicity
  • Demyelinating Diseases* / chemically induced
  • Demyelinating Diseases* / pathology
  • Demyelinating Diseases* / physiopathology
  • Disease Models, Animal
  • Excitatory Postsynaptic Potentials / physiology
  • Female
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neurons* / pathology
  • Neurons* / physiology
  • Oligodendrocyte Precursor Cells* / pathology
  • Oligodendrocyte Precursor Cells* / physiology
  • Oligodendroglia* / physiology
  • Pyramidal Cells / pathology
  • Pyramidal Cells / physiology
  • Synapses* / pathology
  • Synapses* / physiology

Substances

  • Cuprizone