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Generation of an iPSC line (SKLOi001-A) from a patient with CLCN2-related leukoencephalopathy.
Chen, Zhuolin; Peng, Fuhua; Liu, Jia; Xie, Bingbing; Xu, Ping; Gan, Zhouqing; Li, Min; Xu, Li; Zhong, Xiufeng.
Afiliación
  • Chen Z; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Peng F; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.. Electronic address: pengfh@mail.sysu.edu.cn.
  • Liu J; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Xie B; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
  • Xu P; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.
  • Gan Z; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Li M; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Xu L; Department of Neurology, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
  • Zhong X; State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.. Electronic address: xzhong13@qq.com.
Stem Cell Res ; 45: 101769, 2020 05.
Article en En | MEDLINE | ID: mdl-32278302
CLCN2-related leukoencephalopathy (CC2L) is a rare disease due to autosomal recessive loss-of-function mutations in CLCN2 gene. We generated an induced pluripotent stem cell (iPSC) line (SKLOi001-A) from urine cells isolated from a CC2L patient carrying a homozygotic mutation: c.2257C>T (p.Arg753*) in CLCN2 gene via an integration-free methods. The established iPSC line kept the CLCN2 mutation and displayed a normal karyotype, expressed pluripotency markers, showed differentiation potential. This newly iPSC line could be served as a possible tool to unravel the mechanisms underlying CLCN2-associated diseases and screen drugs for the treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Leucoencefalopatías Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre Pluripotentes Inducidas / Leucoencefalopatías Límite: Humans Idioma: En Revista: Stem Cell Res Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido