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从携带复杂杂合、同型校正和纯合 Bloc1s1 突变的个体中生成人类诱导多能干细胞。

Generation of human induced pluripotential stem cells from individuals with complex heterozygous, isogenic corrected, and homozygous Bloc1s1 mutations.

机构信息

Laboratory of Mitochondrial Biology and Metabolism, National Heart Lung and Blood Institute, Bethesda, MD, USA.

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

出版信息

Stem Cell Res. 2022 Oct;64:102905. doi: 10.1016/j.scr.2022.102905. Epub 2022 Aug 30.

Abstract

Genetic studies show that BLOC1S1 modulates mitochondrial and endosome-lysosome function (Wu et al., 2021a). Furthermore, Bloc1s1 mutations are linked to leukodystrophy (Bertoli-Avella et al., 2021). The Vanderver laboratory identified additional individuals with leukodystrophy that harbored either complex heterozygous (Bloc1s1 c.206A > C and c.359G > A), or homozygous (Bloc1s1 c.185 T > C) point mutations. We generated induced pluripotential stem cell (iPSC) lines from these subjects, from parents of the complex heterozygous mutations patient, and from CRISPR isogenic (c.206A > C and c.359G > A) corrected iPSC-line. These complex heterozygous, homozygous, and isogenic-corrected Bloc1s1 lines were phenotypically normal and were capable of differentiation towards the three germ layers.

摘要

遗传研究表明,BLOC1S1 调节线粒体和内体溶酶体功能 (Wu 等人,2021a)。此外,Bloc1s1 突变与脑白质营养不良有关 (Bertoli-Avella 等人,2021)。Vanderver 实验室鉴定了其他患有脑白质营养不良的个体,他们要么携带复杂的杂合突变 (Bloc1s1 c.206A>C 和 c.359G>A),要么携带纯合突变 (Bloc1s1 c.185T>C)。我们从这些受试者、复杂杂合突变患者的父母以及 CRISPR 同基因 (c.206A>C 和 c.359G>A) 校正的 iPSC 系中生成了诱导多能干细胞 (iPSC) 系。这些复杂的杂合子、纯合子和同基因校正的 Bloc1s1 系表型正常,能够向三个胚层分化。

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