Generation of a human induced pluripotent stem cell line (SMUSHi002-A) from an ALS patient carrying a heterozygous mutation c.1562G > A in the FUS gene

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease. Affected patients experience gradual loss of their spinal cord and cortical motor neurons with consequent muscle weakness and emaciation, and eventual respiratory failure. The pathogenesis of ALS remains largely unknown althou...

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Veröffentlicht in:Stem cell research 2024-02, Vol.74, p.103286-103286, Article 103286
Hauptverfasser: Tang, Mei, Xiong, Min, Zhou, Wenyan, Lei, Jiafan, Huang, Min, Huang, Chunyan, Wang, Fei, Liu, Jun, Li, Jun, Xu, Xueqing
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Sprache:eng
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Zusammenfassung:Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease. Affected patients experience gradual loss of their spinal cord and cortical motor neurons with consequent muscle weakness and emaciation, and eventual respiratory failure. The pathogenesis of ALS remains largely unknown although the FUS (sarcoma fusion gene) gene is known to be one of the major pathogenic genes. We have generated an induced pluripotent stem cell line SMUSHi002-A from an ALS patient who carries a heterozygous mutation c.1562G > A in FUS. This cell line will serve as a useful model to investigate disease pathogenesis and develop potential therapeutic approaches for ALS.
ISSN:1873-5061
1876-7753
DOI:10.1016/j.scr.2023.103286