Generation of an induced pluripotent stem cell (iPSC) line (EXSURGi001-A) from a patient homozygous for the p.Ala165Thr mutation in the MTARC1 gene

被引:0
|
作者
Tang, Peter [1 ,2 ]
Keshi, Eriselda [1 ,2 ]
Wilken, Silvana [1 ,2 ]
Wutsdorff, Louise [1 ,2 ]
Mougnekabol, Julienne [1 ,2 ]
Pratschke, Johann [1 ,2 ]
Sauer, Igor M. [1 ,2 ]
Haep, Nils [1 ,2 ,3 ]
机构
[1] Charite Univ Med Berlin, Dept Surg, Campus Virchow Klinikum, Expt Surg, Augustenburger Pl 1, D-13353 Berlin, Germany
[2] Humboldt Univ, Freie Univ Berlin, Augustenburger Pl 1, D-13353 Berlin, Germany
[3] Berlin Inst Hlth Charite BIH, Clinician Scientist Program, Anna Louisa Karsch Str 2, D-10178 Berlin, Germany
关键词
D O I
10.1016/j.scr.2024.103516
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Metabolic dysfunction-associated fatty liver disease (MAFLD), the leading cause of end-stage liver disease in developed countries, is expected to increase over the next decade. Characterized by hepatic steatosis, MAFLD is commonly studied in animal models. Here, we generated a human induced pluripotent stem cell (iPSC) line from a patient homozygous of the protective MTARC1 gene variant rs2642438:A. This line displays a normal karyotype and typical pluripotent stem cell morphology and can differentiate into all three germ layers in vitro. .
引用
收藏
页数:4
相关论文
共 50 条
  • [31] Generation of human induced pluripotent stem cell line (WMUi001-A) from a patient with aortic dissection
    Jin, Peifeng
    Wang, Sixian
    Jiang, Xu
    Shan, Xiaoqiong
    Jiang, Sheng
    Quan, Yingyi
    Zhang, Tianci
    Yang, Jiwen
    Zhang, Huang
    Ma, Jianshe
    Dong, Miaowu
    Fan, Junming
    Fan, Xiaofang
    Gong, Yongsheng
    Wang, Yongyu
    STEM CELL RESEARCH, 2020, 43
  • [32] Generation of a human induced pluripotent stem cell line PUMCi001-A from a patient with Krabbe disease
    Wang, Wei
    Lv, Ya-feng
    Zhang, Yan-jun
    Dong, Wen-ji
    Zhang, Ye
    STEM CELL RESEARCH, 2020, 48
  • [33] Generation of a human induced pluripotent stem cell (iPSC) line (IBMS-iPSC-057-05) from a patient with familial parkinsonism and polyneuropathy having a heterozygous p.Y314S mutation in UQCRC1 gene
    Ou-Yang, Chih-Hsin
    Lin, Han-Yi
    Huang, Cheng-Yen
    Lin, Chin-Hsien
    STEM CELL RESEARCH, 2020, 49
  • [34] An induced pluripotent stem cell line (TRNDi010-C) from a patient carrying a homozygous p.R401X mutation in the NGLY1 gene
    Yang, Shu
    Cheng, Yu-Shan
    Li, Rong
    Pradhan, Manisha
    Hong, Junjie
    Beers, Jeanette
    Zou, Jizhong
    Liu, Chengyu
    Might, Matt
    Rodems, Steven
    Zheng, Wei
    STEM CELL RESEARCH, 2019, 39
  • [35] Generation of induced pluripotent stem cell (iPSC) line from Charcot- Marie- Tooth disease patient with MPZ mutation (CMT1B)
    Son, Daryeon
    Kang, Phil Jun
    Yun, Wonjin
    You, Seungkwon
    STEM CELL RESEARCH, 2017, 24 : 5 - 7
  • [36] Generation of an induced pluripotent stem cell (iPSC) line (BBANTWi009-A) from a Meester-Loeys syndrome patient carrying a BGN mutation
    De Kinderen, Pauline
    Rabaut, Laura
    Hebert, Anne
    Ponsaerts, Peter
    Perik, Melanie
    Meester, Josephina A. N.
    STEM CELL RESEARCH, 2023, 66
  • [37] Generation of a human induced pluripotent stem cell line (iPSC) from peripheral blood mononuclear cells of a patient with a myasthenic syndrome due to mutation in COLQ
    Barbeau, Susie
    Desprat, Romain
    Eymard, Bruno
    Martinat, Cecile
    Lemaitre, Jean-Marc
    Legay, Claire
    STEM CELL RESEARCH, 2020, 49
  • [38] Generation of an induced pluripotent stem cell (iPSC) line SDQLCHi056-A from a patient with Nicolaides-Baraitser syndrome carrying a mutation in SMARCA2 gene
    Yang, Xiaomeng
    Yu, Chunmei
    Gao, Min
    Liu, Yi
    Liu, Yuanxiang
    STEM CELL RESEARCH, 2023, 73
  • [39] Generation of a human induced pluripotent stem cell line (CPGHi001-A) from a hearing loss patient with the TMC1 p.M418K mutation
    Wang, Hongyang
    Wu, Kaiwen
    Guan, Jing
    Wang, Qiuju
    STEM CELL RESEARCH, 2020, 49
  • [40] Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line
    Ma, Ling
    Wu, Ziyan
    Tang, Qingyuan
    Ji, Xiaoli
    Mei, Yuting
    Peng, Ting
    Xu, Qiong
    Zhou, Wenhao
    Xiong, Man
    STEM CELL RESEARCH, 2021, 53