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建立并鉴定 ZJUCHi003 细胞系:一名 Temple-Baraitser/Zimmermann-Laband 综合征患者的诱导多能干细胞系,携带 KCNH1 c.1070G > A(p.R357Q)变异。

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.

机构信息

Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, 310052, China.

Key Laboratory of Genetic and Developmental Disorders of Zhejiang Province, Hangzhou, China.

出版信息

Hum Cell. 2024 May;37(3):832-839. doi: 10.1007/s13577-024-01031-8. Epub 2024 Feb 19.

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.

摘要

KCNH1 基因突变可导致常染色体显性遗传的 Temple-Baraitser/Zimmermann-Laband 综合征,其特征为严重智力障碍、癫痫、牙龈增生和指甲发育不良。本研究利用携带 KCNH1 频发/热点致病性变异 c.1070G > A(p.R357Q)的女孩尿液细胞,建立了一个诱导多能干细胞(iPSC)系。该细胞系命名为 ZJUCHi003,其细胞特征、多能性、核型完整性、无重编程病毒和支原体污染,以及向三个胚层分化的潜能均得到了鉴定和确认。此外,与正常神经元相比,源自 ZJUCHi003 的神经元表现出更慢的动作电位复极化过程和更宽的动作电位半宽度。该细胞系将有助于研究 KCNH1 变异相关症状的发病机制,以及评估新的治疗方法。

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