Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene

Stem Cell Res. 2019 Dec:41:101596. doi: 10.1016/j.scr.2019.101596. Epub 2019 Oct 18.

Abstract

Using a Sendai Virus based vector delivering Yamanaka Factors, we generated induced Pluripotent Stem Cells (iPSCs) from peripheral blood mononuclear cells of a patient affected by Ataxia Telangiectasia (AT), caused by a novel homozygous deletion in ATM, spanning exons 5-7. Three clones were fully characterized for pluripotency and capability to differentiate. These clones preserved the causative mutation of parental cells and genomic stability over time (>100 passages). Furthermore, in AT derived iPSCs we confirmed the impaired DNA damage response after ionizing radiation. All these data underline potential usefulness of our clones as in vitro AT disease model.

MeSH terms

  • Adult
  • Ataxia Telangiectasia / genetics*
  • Ataxia Telangiectasia / pathology*
  • Ataxia Telangiectasia Mutated Proteins / genetics*
  • Cell Differentiation*
  • Cells, Cultured
  • Cellular Reprogramming
  • Female
  • Homozygote
  • Humans
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / pathology*
  • Leukocytes, Mononuclear / metabolism
  • Leukocytes, Mononuclear / pathology*
  • Mutation*
  • Young Adult

Substances

  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins