Generation of two iPSC lines from dilated cardiomyopathy patients with pathogenic variants in the SCN5A gene

Summary

Dilated cardiomyopathy (DCM) is a disorder of cardiac ventricular dilation and contractile dysfunction that often progresses to heart failure. Multiple genes have been associated with DCM, including SCN5A which has been linked to 2 % of all DCM cases. Peripheral mononuclear blood cells from DCM patients with SCN5A variants (c.2440C>T and c.665G>A) were utilized to generate two human induced pluripotent stem cell (iPSC) lines. Both lines exhibited typical iPSC morphology, expressed pluripotency markers, normal karyotypes, and trilineage differentiation capabilities. These lines offer valuable resources for investigating the mechanism of SCN5A-associated DCM, facilitating studies of ion channel protein involvement in the disease. Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Dexheimer R, Manhas A, Wu D, Tripathi D, Yu Chan S, Li J, Yu R, Sayed N, Wu JC, Sallam K
Journal Stem cell research
Publication Date 2024 Oct;80:103498
PubMed 39067410
DOI 10.1016/j.scr.2024.103498

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