Impact of LITAF on Mitophagy and Neuronal Damage in Epilepsy via MCL-1 Ubiquitination

CNS Neurosci Ther. 2025 Jan;31(1):e70191. doi: 10.1111/cns.70191.

Abstract

Objective: This study aims to investigate how the E3 ubiquitin ligase LITAF influences mitochondrial autophagy by modulating MCL-1 ubiquitination, and its role in the development of epilepsy.

Methods: Employing single-cell RNA sequencing (scRNA-seq) to analyze brain tissue from epilepsy patients, along with high-throughput transcriptomics, we identified changes in gene expression. This was complemented by in vivo and in vitro experiments, including protein-protein interaction (PPI) network analysis, western blotting, and behavioral assessments in mouse models.

Results: Neuronal cells in epilepsy patients exhibited significant gene expression alterations, with increased activity in apoptosis-related pathways and decreased activity in neurotransmitter-related pathways. LITAF was identified as a key upregulated factor, inhibiting mitochondrial autophagy by promoting MCL-1 ubiquitination, leading to increased neuronal damage. Knockdown experiments in mouse models further confirmed that LITAF facilitates MCL-1 ubiquitination, aggravating neuronal injury.

Conclusion: Our findings demonstrate that LITAF regulates MCL-1 ubiquitination, significantly impacting mitochondrial autophagy and contributing to neuronal damage in epilepsy. Targeting LITAF and its downstream mechanisms may offer a promising therapeutic strategy for managing epilepsy.

Keywords: LPS‐induced TNF‐alpha factor; MCL1; epilepsy; mitochondrial autophagy; neuroprotection; ubiquitination regulation.

MeSH terms

  • Animals
  • Epilepsy* / metabolism
  • Epilepsy* / pathology
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitophagy* / physiology
  • Myeloid Cell Leukemia Sequence 1 Protein* / genetics
  • Myeloid Cell Leukemia Sequence 1 Protein* / metabolism
  • Neurons* / metabolism
  • Neurons* / pathology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination* / physiology

Substances

  • Myeloid Cell Leukemia Sequence 1 Protein
  • MCL1 protein, human
  • Transcription Factors
  • Nuclear Proteins
  • Ubiquitin-Protein Ligases