Among the known causative genes of familial ALS, SOD1 mutation is one of the most common. It encodes for the ubiquitous detoxifying copper/zinc binding SOD1 enzyme, whose mutations selectively cause motor neuron death, although the mechanisms are not as yet clear. What is known is that mutant-mediated toxicity is not caused by loss of its detoxifying activity but by a gain-of-function. In order to better understand the pathogenic mechanisms of SOD1 mutation, a human induced pluripotent stem cell (hiPSC) line was generated from the somatic cells of a female patient carrying a missense variation in SOD1 (L145F).

Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene / D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Bernardini, L.; Goldoni, M.; Mazzini, L.; De Marchi, F.; Di Pierro, A.; D'Alfonso, S.; Gelati, M.; Vescovi, A. L.; Rosati, J.. - In: STEM CELL RESEARCH. - ISSN 1873-5061. - 47:(2020). [10.1016/j.scr.2020.101924]

Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene

D'Anzi A.;Goldoni M.;Rosati J.
2020

Abstract

Among the known causative genes of familial ALS, SOD1 mutation is one of the most common. It encodes for the ubiquitous detoxifying copper/zinc binding SOD1 enzyme, whose mutations selectively cause motor neuron death, although the mechanisms are not as yet clear. What is known is that mutant-mediated toxicity is not caused by loss of its detoxifying activity but by a gain-of-function. In order to better understand the pathogenic mechanisms of SOD1 mutation, a human induced pluripotent stem cell (hiPSC) line was generated from the somatic cells of a female patient carrying a missense variation in SOD1 (L145F).
2020
SOD1; hiPSC; familial ALS
01 Pubblicazione su rivista::01a Articolo in rivista
Generation of an induced pluripotent stem cell line, CSSi011-A (6534), from an Amyotrophic lateral sclerosis patient with heterozygous L145F mutation in SOD1 gene / D'Anzi, A.; Altieri, F.; Perciballi, E.; Ferrari, D.; Bernardini, L.; Goldoni, M.; Mazzini, L.; De Marchi, F.; Di Pierro, A.; D'Alfonso, S.; Gelati, M.; Vescovi, A. L.; Rosati, J.. - In: STEM CELL RESEARCH. - ISSN 1873-5061. - 47:(2020). [10.1016/j.scr.2020.101924]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1467832
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