Generation of an iPSC cell line (VANYHHi001-A) from a patient with cardiac arrythmias carrying CACNA1D, SCN5A, and DSP variants

被引:0
|
作者
Sleiman, Yvonne [1 ]
Reisqs, Jean-Baptiste [1 ]
Tan, Reina Bianca [2 ]
Cecchin, Frank [2 ]
Chahine, Mohamed [3 ,4 ]
Boutjdir, Mohamed [1 ,5 ,6 ]
机构
[1] VA New York Harbor Healthcare Syst, Cardiovasc Res Program, Brooklyn, NY 11209 USA
[2] NYU Grossman Sch Med, Dept Pediat, Div Pediat Cardiol, New York, NY USA
[3] Inst Univ Sante Mentale Quebec, CERVO Brain Res Ctr, Quebec City, PQ, Canada
[4] Univ Laval, Fac Med, Dept Med, Quebec City, PQ G1V 06A, Canada
[5] SUNY Downstate Hlth Sci Univ, Dept Med Cell Biol & Pharmacol, Brooklyn, NY USA
[6] NYU, Grossman Sch Med, Dept Med, New York, NY USA
关键词
Progressive cardiac conduction defect; Sinoatrial node dysfunction; Induced pluripotent stem cells; SCN5A; CACNA1D; DSP;
D O I
10.1016/j.scr.2024.103608
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Progressive cardiac conduction defect often associated with variants in sodium voltage-gated channel SCN5A gene and variants in the L-type calcium voltage-gated channel CACNA1D gene are implicated in sinoatrial node dysfunction. We generated an induced pluripotent stem cell line (iPSC) from a 13-year-old patient with history of conduction system disease and ventricular tachycardia, carrying variants in SCN5A (c.2618C > G), CACNA1D (c.3786G > T), and DSP (c.1582C > G). The generated iPSC line exhibited pluripotency markers, differentiated into the three embryonic germ layers, and maintained a normal karyotype. This iPSC line offers insights into the pathophysiological mechanisms of cardiac arrhythmias and personalized therapies development.
引用
收藏
页数:5
相关论文
共 43 条
  • [41] Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122*mutations in the AGXT gene
    Martinez-Turrillas, Rebeca
    Rodriguez-Diaz, Saray
    Rodriguez-Marquez, Paula
    Martin-Mallo, Angel
    Salido, Eduardo
    Beck, Bodo B.
    Prosper, Felipe
    Rodriguez-Madoz, Juan R.
    STEM CELL RESEARCH, 2019, 41
  • [42] 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)
    Lu, Ying-qian
    Dong, En-lin
    Yang, Wei-qi
    Lai, Lu-lu
    Lin, Xiao-hong
    Ma, Li-xiang
    Chen, Wan-jin
    Wang, Ning
    Lin, Xiang
    STEM CELL RESEARCH, 2019, 34
  • [43] An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182 T>C ) mutation in the NPC1 gene
    Li, Rong
    Pradhan, Manisha
    Xu, Miao
    Roeder, Amanda
    Beers, Jeanette
    Zou, Jizhong
    Liu, Chengyu
    Porter, Forbes D.
    Zhen, Wei
    STEM CELL RESEARCH, 2020, 44