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建立一个患有原发性纤毛运动障碍的患者的诱导多能干细胞系,该患者携带 CCNO 的双等位基因突变。

Establishment of an induced pluripotent stem cell line from a patient with primary ciliary dyskinesia carrying biallelic mutations in CCNO.

机构信息

Reproductive Medicine Center, Department of Obstetrics and Gynecology, First Affiliated Hospital of Anhui Medical University, No 218 Jixi Road, Hefei 230022, Anhui, China; Anhui Province Key Laboratory of Reproductive Health and Genetics, Anhui Medical University, No 81 Meishan Road, Hefei 230032, Anhui, China; NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract (Anhui Medical University), No 81 Meishan Road, Hefei 230032, Anhui, China.

Reproductive Medicine Center, Department of Obstetrics and Gynecology, First Affiliated Hospital of Anhui Medical University, No 218 Jixi Road, Hefei 230022, Anhui, China; Anhui Province Key Laboratory of Reproductive Health and Genetics, Anhui Medical University, No 81 Meishan Road, Hefei 230032, Anhui, China; NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract (Anhui Medical University), No 81 Meishan Road, Hefei 230032, Anhui, China.

出版信息

Stem Cell Res. 2021 May;53:102372. doi: 10.1016/j.scr.2021.102372. Epub 2021 Apr 29.

Abstract

Primary ciliary dyskinesia (PCD) is an autosomal recessive hereditary disorder affecting motile cilia structure and function, which leads to respiratory diseases and infertility. Here, an induced pluripotent stem cell (iPSC) line of PCD was generated from peripheral blood mononuclear cells of a female patient carrying biallelic mutations in Cyclin O (CCNO) gene. Reprogramming was performed with the non-integrated episomal vectors. The obtained transgene-free iPSCs had normal karyotypes, expressed pluripotency genes, and differentiated into three germ layers. This iPSC line could be a useful guide for studying the pathogenic mechanism, establishing a disease model of PCD, and screening potential therapeutic targets.

摘要

原发性纤毛运动障碍(PCD)是一种常染色体隐性遗传性疾病,影响纤毛的结构和功能,导致呼吸道疾病和不孕。本研究从携带 Cycin O(CCNO)基因双等位基因突变的女性患者外周血单核细胞中诱导生成了 PCD 的诱导多能干细胞(iPSC)系。该过程使用了非整合的附加体载体。获得的无转基因的 iPSC 具有正常的核型,表达多能性基因,并分化为三个胚层。该 iPSC 系可作为研究致病机制、建立 PCD 疾病模型和筛选潜在治疗靶点的有用工具。

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