ATM-deficient neural precursors develop senescence phenotype with disturbances in autophagy

Mech Ageing Dev. 2020 Sep:190:111296. doi: 10.1016/j.mad.2020.111296. Epub 2020 Jul 1.

Abstract

ATM is a kinase involved in DNA damage response (DDR), regulation of response to oxidative stress, autophagy and mitophagy. Mutations in the ATM gene in humans result in ataxi A-Telangiectasia disease (A-T) characterized by a variety of symptoms with neurodegeneration and premature ageing among them. Since brain is one of the most affected organs in A-T, we have focused on senescence of neural progenitor cells (NPCs) derived from A-T reprogrammed fibroblasts. Accordingly, A-T NPCs obtained through neural differentiation of iPSCs in 5% oxygen possessed some features of senescence including increased activity of SA-β-gal and secretion of IL6 and IL8 in comparison to control NPCs. This phenotype of A-T NPC was accompanied by elevated oxidative stress. A-T NPCs exhibited symptoms of impaired autophagy and mitophagy with lack of response to chloroquine treatment. Additional sources of oxidative stress like increased oxygen concentration (20 %) and H2O2 respectively aggravated the phenotype of senescence and additionally disturbed the process of mitophagy. In both cases only A-T NPCs reacted to the treatment. We conclude that oxidative stress may be responsible for the phenotype of senescence and impairment of autophagy in A-T NPCs. Our results point to senescent A-T cells as a potential therapeutic target in this disease.

Keywords: ATM; Ataxia-telangiectasia; Autophagy; Mitophagy; Neural progenitors; Oxidative stress; Senescence; hiPSCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ataxia Telangiectasia / metabolism
  • Ataxia Telangiectasia Mutated Proteins* / deficiency
  • Ataxia Telangiectasia Mutated Proteins* / genetics
  • Ataxia Telangiectasia Mutated Proteins* / metabolism
  • Autophagy / physiology*
  • Cellular Senescence / genetics*
  • DNA Damage
  • Drug Discovery
  • Humans
  • Induced Pluripotent Stem Cells / physiology
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Mitophagy
  • Mutation
  • Neurons / physiology*
  • Oxidative Stress / physiology
  • Signal Transduction
  • beta-Galactosidase / metabolism

Substances

  • Interleukin-6
  • Interleukin-8
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • beta-Galactosidase