A comprehensive library of familial human amyotrophic lateral sclerosis induced pluripotent stem cells

PLoS One. 2015 Mar 11;10(3):e0118266. doi: 10.1371/journal.pone.0118266. eCollection 2015.

Abstract

Amyotrophic lateral sclerosis is a progressive disease characterized by the loss of upper and lower motor neurons, leading to paralysis of voluntary muscles. About 10% of all ALS cases are familial (fALS), among which 15-20% are linked to Cu/Zn superoxide dismutase (SOD1) mutations, usually inherited in an autosomal dominant manner. To date only one FDA approved drug is available which increases survival moderately. Our understanding of ALS disease mechanisms is largely derived from rodent model studies, however due to the differences between rodents and humans, it is necessary to have humanized models for studies of disease pathogenesis as well as drug development. Therefore, we generated a comprehensive library of a total 22 of fALS patient-specific induced pluripotent stem cell (iPSC) lines. These cells were thoroughly characterized before being deposited into the library. The library of cells includes a variety of C9orf72 mutations, sod1 mutations, FUS, ANG and FIG4 mutations. Certain mutations are represented with more than one line, which allows for studies of variable genetic backgrounds. In addition, these iPSCs can be successfully differentiated to astroglia, a cell type known to play a critical role in ALS disease progression. This library represents a comprehensive resource that can be used for ALS disease modeling and the development of novel therapeutics.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Adult
  • Aged
  • Amyotrophic Lateral Sclerosis / genetics
  • Amyotrophic Lateral Sclerosis / pathology*
  • Astrocytes / metabolism
  • C9orf72 Protein
  • Cell Differentiation
  • Cells, Cultured
  • Female
  • Humans
  • Induced Pluripotent Stem Cells / physiology*
  • Male
  • Middle Aged
  • Mutation
  • Proteins / genetics
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase-1
  • Tissue Banks*

Substances

  • C9orf72 Protein
  • C9orf72 protein, human
  • Proteins
  • SOD1 protein, human
  • Superoxide Dismutase
  • Superoxide Dismutase-1