Generation of two familial hypercholesterolemia patient-specific induced pluripotent stem cell lines harboring heterozygous mutations in the LDLR gene
Summary
Familial hypercholesterolemia (FH) is a genetic disorder affecting the metabolism of lipoprotein, characterized by elevated levels of plasma concentrations of low-density lipoprotein cholesterol (LDLC). The most common FH cause is mutations within the gene that encodes for the LDL receptor (LDLR) protein. Two induced pluripotent stem cell (iPSC) lines were generated from patients with FH, each carrying a single heterozygous mutation in the LDLR gene, one is a missense mutation, c.631C > T, and the other is a splice-site mutation, c.313 + 1G > A. Both iPSC lines exhibited strong expression of pluripotency markers, demonstrated the ability to differentiate into derivatives of the three germ layers, and maintained normal karyotypes. These derived iPSC lines represent powerful tools for in vitro modeling FH and offer a promising platform for therapeutic development. Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.
| Authors | Gao J, Li J, Xu L, Yan CD, Knowles JW, Wu JC |
|---|---|
| Journal | Stem cell research |
| Publication Date | 2024 Aug;78:103463 |
| PubMed | 38852422 |
| PubMed Central | PMC11532021 |
| DOI | 10.1016/j.scr.2024.103463 |