Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation

Long QT syndrome (LQT) is an inherited primary arrhythmic disorder characterized by prolonged QT interval on the surface electrocardiogram and life-threatening arrhythmia. In this study, a skin biopsy was obtained from an LQT type 2 (LQT2) patient, who carried a nonsense mutation (c.1956C > A; p....

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Main Authors: Fengfeng Guo, Yaxun Sun, Hongkun Wang, Hao Wang, Jingjun Zhou, Hangping Fan, Jun Su, Tingyu Gong, Chenyang Jiang, Ping Liang
Format: Article
Language:English
Published: Elsevier 2022-07-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506122001623
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author Fengfeng Guo
Yaxun Sun
Hongkun Wang
Hao Wang
Jingjun Zhou
Hangping Fan
Jun Su
Tingyu Gong
Chenyang Jiang
Ping Liang
author_facet Fengfeng Guo
Yaxun Sun
Hongkun Wang
Hao Wang
Jingjun Zhou
Hangping Fan
Jun Su
Tingyu Gong
Chenyang Jiang
Ping Liang
author_sort Fengfeng Guo
collection DOAJ
description Long QT syndrome (LQT) is an inherited primary arrhythmic disorder characterized by prolonged QT interval on the surface electrocardiogram and life-threatening arrhythmia. In this study, a skin biopsy was obtained from an LQT type 2 (LQT2) patient, who carried a nonsense mutation (c.1956C > A; p.Y652X) in the potassium voltage-gated channel subfamily H member 2 (KCNH2) gene. The skin fibroblasts were reprogrammed by non-integrated Sendai viral method to generate a patient-specific induced pluripotent stem cell (iPSC) line. The generated iPSC line showed typical embryonic stem cell-like morphology, exhibited normal karyotype, expressed pluripotency markers, and was capable to differentiate into three germ layers.
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spelling doaj.art-6a2b884e7a2e48bebf40b6996c58cd422022-12-22T02:32:07ZengElsevierStem Cell Research1873-50612022-07-0162102813Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutationFengfeng Guo0Yaxun Sun1Hongkun Wang2Hao Wang3Jingjun Zhou4Hangping Fan5Jun Su6Tingyu Gong7Chenyang Jiang8Ping Liang9Key Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaDepartment of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, ChinaKey Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaDepartment of Prenatal Diagnosis (Screening) Center, Hangzhou Women's Hospital (Hangzhou Maternity and Child Health Care Hospital), Hangzhou 310008, ChinaKey Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaKey Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaKey Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaKey Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, ChinaDepartment of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou 310016, China; Corresponding authors at: 79 Qingchun Road, Hangzhou 310003, China (Ping Liang); 3 Qingchun East Road, Hangzhou 310016, China (Chenyang Jiang).Key Laboratory of Combined Multi-organ Transplantation, Ministry of Public Health, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China; Institute of Translational Medicine, Zhejiang University, Hangzhou 310029, China; Corresponding authors at: 79 Qingchun Road, Hangzhou 310003, China (Ping Liang); 3 Qingchun East Road, Hangzhou 310016, China (Chenyang Jiang).Long QT syndrome (LQT) is an inherited primary arrhythmic disorder characterized by prolonged QT interval on the surface electrocardiogram and life-threatening arrhythmia. In this study, a skin biopsy was obtained from an LQT type 2 (LQT2) patient, who carried a nonsense mutation (c.1956C > A; p.Y652X) in the potassium voltage-gated channel subfamily H member 2 (KCNH2) gene. The skin fibroblasts were reprogrammed by non-integrated Sendai viral method to generate a patient-specific induced pluripotent stem cell (iPSC) line. The generated iPSC line showed typical embryonic stem cell-like morphology, exhibited normal karyotype, expressed pluripotency markers, and was capable to differentiate into three germ layers.http://www.sciencedirect.com/science/article/pii/S1873506122001623
spellingShingle Fengfeng Guo
Yaxun Sun
Hongkun Wang
Hao Wang
Jingjun Zhou
Hangping Fan
Jun Su
Tingyu Gong
Chenyang Jiang
Ping Liang
Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
Stem Cell Research
title Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
title_full Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
title_fullStr Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
title_full_unstemmed Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
title_short Generation of an induced pluripotent stem cell line from a long QT syndrome patient carrying KCNH2/1956C > A mutation
title_sort generation of an induced pluripotent stem cell line from a long qt syndrome patient carrying kcnh2 1956c a mutation
url http://www.sciencedirect.com/science/article/pii/S1873506122001623
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