Derivation of YCMi005-A, a human-induced pluripotent stem cell line, from a patient with dilated cardiomyopathy carrying missense variant in TPM1 (p. Glu192Lys)


Dilated cardiomyopathy (DCM) is one of the leading causes of heart transplantation. The clinical feature of DCM is characterized by enlarged heart and impaired function of the left or both ventricles, while its etiology is varied. In this study, we generated YCMi005-A, a human-induced pluripotent stem cell (hiPSC) line from a patient with DCM carrying the missense mutation of p.Glu192Lys in the TPM1 genes. YCMi005-A, an established hiPSC, showed the normal karyotype (46, XX) and high expression of pluripotency markers. In addition, it was confirmed that YCMi005-A has the differentiation potential assessed by staining of three germ layer markers. Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Authors Cha YJ, Jeon SB, Oh J, Lee ST, Kim S, Kim H, Choi J, Choi HK, Won D, Choi JR, Kim SJ, Park SW, Kang SM, Lee SH
Journal Stem cell research
Publication Date 2022 Apr;60:102707
PubMed 35176663
DOI 10.1016/j.scr.2022.102707

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