Generation of an induced pluripotent stem cell line (ZZUi036-A) derived from skin fibroblasts of a Neuronal intranuclear inclusion disease patient with GGC repeat expansion in the NOTCH2NLC gene

Stem Cell Res. 2022 Aug:63:102844. doi: 10.1016/j.scr.2022.102844. Epub 2022 Jun 15.

Abstract

Neuronal intranuclear inclusion disease (NIID) is a neurodegenerative disease characterized by cognitive impairment, extrapyramidal symptoms, white matter lesions and muscle weakness. The cause of NIID is a repeat amplification of a GGC mutation in the 5 ' untranslated region (UTR) of the NOTCH2NLC gene. Using the non-integrating Sendai virus to deliver the Klf4, OCT3/4, SOX2 and C-MYC factors, fibroblasts obtained from a NIID patient were reprogrammed to generate an induced pluripotent stem cell (iPSC) line (ZZUi036-A). Our approach provided a resource for the investigation of the mechanism of the disease, drug research, cell transplantation and gene therapy.

MeSH terms

  • Fibroblasts / pathology
  • Humans
  • Induced Pluripotent Stem Cells* / metabolism
  • Intranuclear Inclusion Bodies / genetics
  • Intranuclear Inclusion Bodies / pathology
  • Neurodegenerative Diseases* / genetics
  • Neurodegenerative Diseases* / pathology
  • Trinucleotide Repeat Expansion / genetics

Supplementary concepts

  • Neuronal intranuclear inclusion disease