Establishment of human embryonic stem cell WAe009-A-88 carrying a long QT syndrome mutation in KCNH2

Summary

Long-QT syndrome type 2 (LQT2) is a life-threatening Mendelian disease caused by genetic variants in KCNH2. Herein, we generated a human embryonic stem cell line (WAe009-A-88) carrying a LQT2 related mutation in KCNH2, c.1720 A>G. The WAe009-A-88 line maintained stem cell-like morphology, expressed high levels of pluripotent markers, had a normal karyotype, and could differentiate into all three germ layers in vivo. The cell line can serve as valuable tools for modeling LQT2 in vitro and investigating the pathological mechanisms related to KCNH2 mutations. Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Wen H, Sun L, Zhong J, Wu F
Journal Stem cell research
Publication Date 2022 Apr 28;62:102795
PubMed 35526388
DOI 10.1016/j.scr.2022.102795

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