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利用CRISPR/Cas9从人胚胎干细胞系产生FOS基因敲除系。

Generation of FOS gene knockout lines from a human embryonic stem cell line using CRISPR/Cas9.

作者信息

Li Chunfu, Wang Qing, Peng Zhiyong, Lin Yuchen, Liu Huaying, Yang Xiuling, Li Shan, Liu XiaoTing, Chen Jingru

机构信息

Department of Pediatrics, Nanfang Hospital, Southern Medical University, GuangZhou, China.

Department of Pediatrics, Nanfang Hospital, Southern Medical University, GuangZhou, China.

出版信息

Stem Cell Res. 2019 Aug;39:101479. doi: 10.1016/j.scr.2019.101479. Epub 2019 Jun 5.

Abstract

FOS is component of the AP-1 complex and has been reported to be involved in many cellular functions, including cell proliferation, differentiation, survival, angiogenesis, hematopoiesis and cancer progress. To further understand the exact role of FOS in these processes, here we created two FOS knockout human embryonic stem cell lines by CRISPR/Cas9 mediated gene targeting. These cell lines retained normal morphology and karyotype, normal expression of pluripotent markers, and differentiation potential both in vivo and in vitro. These cell lines can be used to verify whether the FOS mutated produces any affect on endothelial cells and hematopoietic progenitor cells during the hematopoietic differentiation.

摘要

FOS是AP-1复合物的组成部分,据报道它参与许多细胞功能,包括细胞增殖、分化、存活、血管生成、造血和癌症进展。为了进一步了解FOS在这些过程中的具体作用,我们在此通过CRISPR/Cas9介导的基因靶向创建了两条FOS基因敲除的人类胚胎干细胞系。这些细胞系保持正常的形态和核型、多能性标志物的正常表达以及体内和体外的分化潜能。这些细胞系可用于验证FOS突变在造血分化过程中是否对内皮细胞和造血祖细胞产生任何影响。

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