Ataxia Telangiectasia patient-derived neuronal and brain organoid models reveal mitochondrial dysfunction and oxidative stress

Neurobiol Dis. 2024 Sep:199:106562. doi: 10.1016/j.nbd.2024.106562. Epub 2024 Jun 13.

Abstract

Ataxia Telangiectasia (AT) is a rare disorder caused by mutations in the ATM gene and results in progressive neurodegeneration for reasons that remain poorly understood. In addition to its central role in nuclear DNA repair, ATM operates outside the nucleus to regulate metabolism, redox homeostasis and mitochondrial function. However, a systematic investigation into how and when loss of ATM affects these parameters in relevant human neuronal models of AT was lacking. We therefore used cortical neurons and brain organoids from AT-patient iPSC and gene corrected isogenic controls to reveal levels of mitochondrial dysfunction, oxidative stress, and senescence that vary with developmental maturity. Transcriptome analyses identified disruptions in regulatory networks related to mitochondrial function and maintenance, including alterations in the PARP/SIRT signalling axis and dysregulation of key mitophagy and mitochondrial fission-fusion processes. We further show that antioxidants reduce ROS and restore neurite branching in AT neuronal cultures, and ameliorate impaired neuronal activity in AT brain organoids. We conclude that progressive mitochondrial dysfunction and aberrant ROS production are important contributors to neurodegeneration in AT and are strongly linked to ATM's role in mitochondrial homeostasis regulation.

Keywords: Ataxia telangiectasia; Brain organoids; Cellular senescence; Mitochondria; Neurodegeneration; Oxidative stress.

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins / genetics
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Ataxia Telangiectasia* / genetics
  • Ataxia Telangiectasia* / metabolism
  • Ataxia Telangiectasia* / pathology
  • Brain* / metabolism
  • Brain* / pathology
  • Humans
  • Induced Pluripotent Stem Cells* / metabolism
  • Mitochondria* / metabolism
  • Mitochondria* / pathology
  • Neurons* / metabolism
  • Neurons* / pathology
  • Organoids* / metabolism
  • Oxidative Stress* / physiology
  • Reactive Oxygen Species / metabolism

Substances

  • Ataxia Telangiectasia Mutated Proteins
  • Reactive Oxygen Species