Literature DB >> 30611022

Generation of an integration-free induced pluripotent stem cell line, FJMUi001-A, from a hereditary spastic paraplegia patient carrying compound heterozygous p.P498L and p.R618W mutations in CAPN1 (SPG76).

Ying-Qian Lu1, En-Lin Dong1, Wei-Qi Yang2, Lu-Lu Lai1, Xiao-Hong Lin1, Li-Xiang Ma2, Wan-Jin Chen3, Ning Wang3, Xiang Lin4.   

Abstract

The human iPS cell line, hiPS-SPG76 (FJMUi001-A), derived from skin fibroblasts from a 42-year-old male hereditary spastic paraplegia patient carrying compound heterozygous p.P498L (c.1493C > T) and p.R618W (c.1852C > T) mutations in the CAPN1 gene, was generated by non-integrative reprogramming vectors encoding OCT3/4, SOX2, KLF4, and c-MYC. The established hiPS-SPG76 was free of genomically integrated reprogramming genes, had a normal karyotype, expressed pluripotency markers, and had capacity to form three germ layers in vitro and in vivo. This generated hiPS cell line offers a useful resource to study the pathogenesis of SPG76.
Copyright © 2018 The Authors. Published by Elsevier B.V. All rights reserved.

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Year:  2018        PMID: 30611022     DOI: 10.1016/j.scr.2018.11.015

Source DB:  PubMed          Journal:  Stem Cell Res        ISSN: 1873-5061            Impact factor:   2.020


  1 in total

1.  Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement.

Authors:  Min-Yu Lan; Chin-Song Lu; Shey-Lin Wu; Ying-Fa Chen; Yueh-Feng Sung; Min-Chien Tu; Yung-Yee Chang
Journal:  Front Neurol       Date:  2022-09-30       Impact factor: 4.086

  1 in total

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