Disruption of ClC-3-mediated 2Cl-/H+ exchange leads to behavioural deficits and thalamic atrophy

Sci Rep. 2025 Sep 29;15(1):33326. doi: 10.1038/s41598-025-19757-2.

Abstract

CLCN3 encodes ClC-3, an endosomal 2Cl⁻/H⁺ exchanger, with pathogenic variants causing a neurodevelopmental condition marked by developmental delays, intellectual disability, seizures, hyperactivity, anxiety, and brain and retinal abnormalities. Clcn3-/- mice show hippocampal and retinal degeneration, recapitulating key symptoms observed in humans. ClC-3 forms homodimers (ClC-3/ClC-3) and heterodimers with ClC-4 (ClC-3/ClC-4), with overlapping brain expression. This suggests distinct functional roles for homo- and heterodimeric assemblies and raises the question of which brain regions specifically depend on ClC-3/ClC-3 rather than ClC-3/ClC-4 complexes. Using ex vivo PET tracer analyses, Clcn3-/- and Clcn3td/td mice, we found neurodegeneration in the hippocampus and thalamus of Clcn3-/-, while Clcn3td/td mice showed thalamic degeneration and altered neuronal excitability, including changes in action potential threshold and after hyperpolarization. Clcn3td/td mice carrying a transport-deficient p.E281Q ClC-3 variant that still associates with ClC-4, thereby allowing ClC-4 to be sorted to endosomes as ClC-4/ClC-3 heterodimers, unlike in the Clcn3-/- model. Clcn3td/td mice also exhibited reduced weight, hyperactivity, and motor deficits, reflecting clinical features. Lower ClC-4 levels in thalamus predict a predominant thalamic expression of ClC-3/ClC-3 homodimers. Overall, our findings indicate a region-specific function of ClC-3/ClC-3 homodimeric complexes and highlight the importance of ClC-3 transport activity in thalamic neuron survival, with electrophysiological dysfunction likely contributing to neurodegeneration.

Keywords: CLCN3; Action potentials; Behavioural deficits; Chloride/proton exchanger; Thalamic neurodegeneration.

MeSH terms

  • Animals
  • Atrophy
  • Behavior, Animal
  • Chloride Channels* / genetics
  • Chloride Channels* / metabolism
  • Hippocampus / metabolism
  • Hippocampus / pathology
  • Humans
  • Mice
  • Mice, Knockout
  • Thalamus* / diagnostic imaging
  • Thalamus* / metabolism
  • Thalamus* / pathology

Substances

  • Chloride Channels
  • ClC-3 channel