Generation of iPSC line NCHi015-A from a patient with truncus arteriosus carrying heterozygous variants in KMT2D and NOTCH1

Summary

Truncus arteriosus (TA) is a congenital heart defect where one main blood vessel emerges from the heart, instead of individual aorta and pulmonary artreries. Peripheral mononuclear cells (PBMCs) of a male infant with TA were reporogrammed using Sendai virus. The resultant iPSC line (NCHi015-A) displayed normal colony formation, expressed pluripotency markers, and differentiated into cells from three germ layers. NCHi015-A was matched to the patient's genetic profile, had normal karyotype, retained genetic variants in KMT2D and NOTCH1, and tested negative for reprogramming transgene. This iPSC line can be used for studying congenital heart defects associated with genetic variants in KMT2D and NOTCH1. Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.

Authors Wang J, Bering J, Alonzo M, Ye S, Texter K, Garg V, Zhao MT
Journal Stem cell research
Publication Date 2024 Aug;78:103457
PubMed 38833814
PubMed Central PMC11193886
DOI 10.1016/j.scr.2024.103457

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