Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76)

Stem Cell Res. 2019 Jan:34:101354. doi: 10.1016/j.scr.2018.11.015. Epub 2018 Nov 27.

Abstract

The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old male hereditary spastic paraplegia patient carrying compound heterozygous p.P498L (c.1493C > T) and p.R618W (c.1852C > T) mutations in the CAPN1 gene, was generated by non-integrative reprogramming vectors encoding OCT3/4, SOX2, KLF4, and c-MYC. The established hiPS-SPG76 was free of genomically integrated reprogramming genes, had a normal karyotype, expressed pluripotency markers, and had capacity to form three germ layers in vitro and in vivo. This generated hiPS cell line offers a useful resource to study the pathogenesis of SPG76.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Base Sequence
  • Calpain / genetics*
  • Cell Culture Techniques / methods*
  • Cell Line
  • Heterozygote
  • Humans
  • Induced Pluripotent Stem Cells / pathology*
  • Kruppel-Like Factor 4
  • Male
  • Mutation / genetics*
  • Spastic Paraplegia, Hereditary / genetics*
  • Spastic Paraplegia, Hereditary / pathology*

Substances

  • KLF4 protein, human
  • Kruppel-Like Factor 4
  • Calpain
  • CAPN1 protein, human