Generation of a human SLC12A3 knock-in human induced pluripotent stem cell line (CMCi014-A-82) using CRISPR-Cas9 system
Summary
Gitelman's disease is caused by a genetic mutation in the solute carrier family 12 member 3 (SLC12A3) gene, which encodes the sodium chloride cotransporter. In this study, we generated a stable human induced pluripotent stem cell (hiPSC) line, WTC11-SLC12A3 (CMCi014-A-82), by knocking in the entire SLC12A3 gene at the SHS231 locus in healthy wild-type control hiPSCs (WTC11). We verified that WTC11-SLC12A3 expressed pluripotency markers and exhibited normal stem cell morphology. Furthermore, this cell line maintains a normal karyotype and can differentiate into the three germ layers. Therefore, this cell line may provide a basis for gene therapy for Gitelman's disease. Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.
Authors | Woo Lim S, In Lee K, Cui S, Fang X, Jin Shin Y, Lee H, Woo Yang C, Young Lee J, Ha Chung B |
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Journal | Stem cell research |
Publication Date | 2024 Dec;81:103522 |
PubMed | 39163808 |
DOI | 10.1016/j.scr.2024.103522 |