Generation of an integration-free iPSC line, ICCSICi006-A, derived from a male Alzheimer's disease patient carrying the PSEN1-G206D mutation

Eva Díaz-Guerra, Manuel A. Oria-Muriel, Elena P. Moreno-Jiménez, Itziar de Rojas, César Rodríguez, Eva Rodríguez-Traver, María Orera, Isabel Hernández, Agustín Ruiz, Carlos Vicario

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

The familial form of Alzheimer's disease (FAD), which is caused by mutations in PRESENILIN 1 (PSEN1) and amyloid precursor protein (APP) genes, represents less than 5% of all AD cases and has an early-onset. We report the generation and characterization of an iPSC line derived from a FAD patient carrying the PSEN1-G206D mutation. The iPSC line maintained the original genotype, a normal karyotype, was free from Sendai viral vectors and reprogramming factors (OCT4, SOX2, KLF4 and c-MYC), presented a typical morphology, expressed endogenous pluripotency markers, and could be differentiated into ectodermal, mesodermal and endodermal cells, confirming its pluripotency.

Original languageEnglish (US)
Article number101574
JournalStem Cell Research
Volume40
DOIs
StatePublished - Oct 2019
Externally publishedYes

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology

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