Dysregulation of zebrin-II cell subtypes in the cerebellum is a shared feature across polyglutamine ataxia mouse models and patients

Sci Transl Med. 2024 Nov 6;16(772):eadn5449. doi: 10.1126/scitranslmed.adn5449. Epub 2024 Nov 6.

Abstract

Spinocerebellar ataxia type 7 (SCA7) is a genetic neurodegenerative disorder caused by a CAG-polyglutamine repeat expansion. Purkinje cells (PCs) are central to the pathology of ataxias, but their low abundance in the cerebellum underrepresents their transcriptomes in sequencing assays. To address this issue, we developed a PC enrichment protocol and sequenced individual nuclei from mice and patients with SCA7. Single-nucleus RNA sequencing in SCA7-266Q mice revealed dysregulation of cell identity genes affecting glia and PCs. Specifically, genes marking zebrin-II PC subtypes accounted for the highest proportion of DEGs in symptomatic SCA7-266Q mice. These transcriptomic changes in SCA7-266Q mice were associated with increased numbers of inhibitory synapses as quantified by immunohistochemistry and reduced spiking of PCs in acute brain slices. Dysregulation of zebrin-II cell subtypes was the predominant signal in PCs of SCA7-266Q mice and was associated with the loss of zebrin-II striping in the cerebellum at motor symptom onset. We furthermore demonstrated zebrin-II stripe degradation in additional mouse models of polyglutamine ataxia and observed decreased zebrin-II expression in the cerebella of patients with SCA7. Our results suggest that a breakdown of zebrin subtype regulation is a shared pathological feature of polyglutamine ataxias.

MeSH terms

  • Animals
  • Ataxia / genetics
  • Ataxia / metabolism
  • Ataxia / pathology
  • Cerebellum* / metabolism
  • Cerebellum* / pathology
  • Disease Models, Animal*
  • Humans
  • Mice
  • Mice, Transgenic
  • Nerve Tissue Proteins* / genetics
  • Nerve Tissue Proteins* / metabolism
  • Peptides* / metabolism
  • Purkinje Cells* / metabolism
  • Purkinje Cells* / pathology
  • Spinocerebellar Ataxias / genetics
  • Spinocerebellar Ataxias / metabolism
  • Spinocerebellar Ataxias / pathology
  • Synapses / metabolism
  • Synapses / pathology
  • Transcriptome / genetics

Substances

  • polyglutamine
  • Nerve Tissue Proteins
  • zebrin II
  • Peptides