Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant

Francesco Martello, Serena Lattante*, Paolo Niccolo' Doronzio, Amelia Conte, Giulia Bisogni, Daniela Orteschi, Filomena Pirozzi, Mario Sabatelli, Marcella Zollino, Giuseppe Marangi

*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease affecting upper and lower motor neurons. We generated patient-derived-induced Pluripotent Stem Cells (iPSCs), from an ALS patient affected by an early-onset and aggressive form of the disease, carrying a missense pathogenic variant in FUS gene. We reprogrammed somatic cells using an established Sendai virus protocol and we obtained clones of iPSC. We confirmed their stemness and further generated embryoid bodies, showing their potential of differentiating in all three germ layers. This iPSC line, carrying a pathogenic FUS variant, is a valuable tool to deeply investigate pathogenic mechanisms leading to ALS.
Lingua originaleEnglish
pagine (da-a)102461-N/A
RivistaStem Cell Research
Volume55
DOI
Stato di pubblicazionePubblicato - 2021

Keywords

  • Amyotrophic Lateral Sclerosis
  • Amyotrophic lateral sclerosis, FUS, Sendai virus
  • Humans
  • Induced Pluripotent Stem Cells
  • Motor Neurons
  • Neurodegenerative Diseases
  • RNA-Binding Protein FUS

Fingerprint

Entra nei temi di ricerca di 'Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variant'. Insieme formano una fingerprint unica.

Cita questo