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Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant.
Chen, Die; Su, Jimei; Huang, Xueying; Chen, Hongyu; Jiang, Tiejia; Zhi, Chunchun; Zhou, Zuolin; Zhang, Bing; Yu, Lan; Jiang, Xiaoling.
Affiliation
  • Chen D; Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Su J; Key Laboratory of Genetic and Developmental Disorders of Zhejiang Province, Hangzhou, China.
  • Huang X; Department of Stomatology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Chen H; Shanghai Key Laboratory of Maternal Fetal Medicine, Clinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, School of Medicine, Shanghai Institute of Maternal-Fetal Medicine and Gynecologic Oncology, Tongji University, Shanghai, 201204, China.
  • Jiang T; Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Zhi C; Department of Neurology, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Zhou Z; Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Zhang B; Key Laboratory of Genetic and Developmental Disorders of Zhejiang Province, Hangzhou, China.
  • Yu L; Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.
  • Jiang X; Key Laboratory of Genetic and Developmental Disorders of Zhejiang Province, Hangzhou, China.
Hum Cell ; 37(3): 832-839, 2024 May.
Article in En | MEDLINE | ID: mdl-38372889
ABSTRACT
Pathogenic variants of the KCNH1 gene can cause dominant-inherited Temple-Baraitser/Zimmermann-Laband syndrome with severe mental retardation, seizure, gingival hyperplasia and nail hypoplasia. This study established an induced pluripotent stem cell (iPSC) line using urinary cells from a girl with KCNH1 recurrent/hotspot pathogenic variant c.1070G > A (p.R357Q). The cell identity, pluripotency, karyotypic integrity, absence of reprogramming virus and mycoplasma contamination, and differential potential to three germ layers of the iPSC line, named as ZJUCHi003, were characterized and confirmed. Furthermore, ZJUCHi003-derived neurons manifested slower action potential repolarization process and wider action potential half-width than the normal neurons. This cell line will be useful for investigating the pathogenic mechanisms of KCNH1 variants-associated symptoms, as well as for evaluating novel therapeutic approaches.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thumb / Abnormalities, Multiple / Hand Deformities, Congenital / Hallux / Craniofacial Abnormalities / Induced Pluripotent Stem Cells / Fibromatosis, Gingival / Intellectual Disability / Nails, Malformed Limits: Female / Humans Language: En Journal: Hum Cell Year: 2024 Document type: Article Affiliation country: China Country of publication: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thumb / Abnormalities, Multiple / Hand Deformities, Congenital / Hallux / Craniofacial Abnormalities / Induced Pluripotent Stem Cells / Fibromatosis, Gingival / Intellectual Disability / Nails, Malformed Limits: Female / Humans Language: En Journal: Hum Cell Year: 2024 Document type: Article Affiliation country: China Country of publication: Japan