Frontiers in Cellular Neuroscience (Feb 2024)

Characterization of hyperpolarization-activated cyclic nucleotide-gated channels in oligodendrocytes

  • Kyle A. Lyman,
  • Ye Han,
  • Andrew P. Robinson,
  • Samuel E. Weinberg,
  • Daniel W. Fisher,
  • Robert J. Heuermann,
  • Reagan E. Lyman,
  • Dong Kyu Kim,
  • Dong Kyu Kim,
  • Dong Kyu Kim,
  • Dong Kyu Kim,
  • Andreas Ludwig,
  • Navdeep S. Chandel,
  • Mark D. Does,
  • Mark D. Does,
  • Mark D. Does,
  • Mark D. Does,
  • Stephen D. Miller,
  • Dane M. Chetkovich

DOI
https://doi.org/10.3389/fncel.2024.1321682
Journal volume & issue
Vol. 18

Abstract

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Mature oligodendrocytes (OLG) are the myelin-forming cells of the central nervous system. Recent work has shown a dynamic role for these cells in the plasticity of neural circuits, leading to a renewed interest in voltage-sensitive currents in OLG. Hyperpolarization-activated cyclic nucleotide-gated (HCN) channels and their respective current (Ih) were recently identified in mature OLG and shown to play a role in regulating myelin length. Here we provide a biochemical and electrophysiological characterization of HCN channels in cells of the oligodendrocyte lineage. We observed that mice with a nonsense mutation in the Hcn2 gene (Hcn2ap/ap) have less white matter than their wild type counterparts with fewer OLG and fewer oligodendrocyte progenitor cells (OPCs). Hcn2ap/ap mice have severe motor impairments, although these deficits were not observed in mice with HCN2 conditionally eliminated only in oligodendrocytes (Cnpcre/+; Hcn2F/F). However, Cnpcre/+; Hcn2F/F mice develop motor impairments more rapidly in response to experimental autoimmune encephalomyelitis (EAE). We conclude that HCN2 channels in OLG may play a role in regulating metabolism.

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