来自两个家族的5个个体的诱导多能干细胞系,携带致病性荷兰MYBPC3创始人变异,不同程度的肥厚性心肌病

IF 0.8 4区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Floor W. van den Dolder , Vincent A.J. Warnaar , Yeszamin L. Onderwater , Annette F. Baas , Diederik W.D. Kuster , Jolanda van der Velden
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引用次数: 0

摘要

肥厚性心肌病(HCM)通常由致病性或可能致病性变异引起,其中30 - 50%涉及编码心肌肌球蛋白结合蛋白c (MYBPC3)的基因变异。我们从两个家族的5个个体中获得了人诱导多能干细胞系,这些个体携带致病性荷兰MYBPC3创始人变异:c.2373insG (n = 2)和c.2827C >;T (n = 3),具有高度可变的疾病表达。外周血单核细胞用外泌质粒重编程。所有细胞系均表达多能性标记,表现出正常的核型,并能在体外分化为各胚层的衍生物。这些细胞系可作为研究HCM发病机制的疾病模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Generation of induced pluripotent stem cell lines from five individuals from two families carrying a pathogenic Dutch MYBPC3 founder variant with variable degrees of hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is often caused by pathogenic or likely pathogenic variants, of which 30–50 % involve a variant in the gene encoding cardiac myosin-binding protein-C (MYBPC3). We generated human induced pluripotent stem cell lines from five individuals from two families carrying a pathogenic Dutch MYBPC3 founder variant: c.2373insG (n = 2) and c.2827C > T (n = 3), with highly variable disease expression. Peripheral blood mononuclear cells were reprogrammed using episomal plasmids. All cell lines express pluripotent markers, exhibit a normal karyotype, and could differentiate into derivatives of each germ layers in vitro. These cell lines can serve as disease model to investigate HCM pathogenesis.
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来源期刊
Stem cell research
Stem cell research 生物-生物工程与应用微生物
CiteScore
2.20
自引率
8.30%
发文量
338
审稿时长
55 days
期刊介绍: Stem Cell Research is dedicated to publishing high-quality manuscripts focusing on the biology and applications of stem cell research. Submissions to Stem Cell Research, may cover all aspects of stem cells, including embryonic stem cells, tissue-specific stem cells, cancer stem cells, developmental studies, stem cell genomes, and translational research. Stem Cell Research publishes 6 issues a year.
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