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 originale | Inglese |
|---|---|
| pagine (da-a) | 102461-N/A |
| Rivista | Stem Cell Research |
| Volume | 55 |
| Numero di pubblicazione | N/A |
| DOI | |
| Stato di pubblicazione | Pubblicato - 2021 |
All Science Journal Classification (ASJC) codes
- Biologia dello Sviluppo
- Biologia Cellulare
Keywords
- Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis
- FUS
- Humans
- Induced Pluripotent Stem Cells
- Motor Neurons
- Neurodegenerative Diseases
- RNA-Binding Protein FUS
- Sendai virus
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