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利用CRISPR-Cas9通过内源性基因激活控制间充质干细胞中的脂肪生成分化

Control of Adipogenic Differentiation in Mesenchymal Stem Cells via Endogenous Gene Activation Using CRISPR-Cas9.

作者信息

Furuhata Yuichi, Nihongaki Yuta, Sato Moritoshi, Yoshimoto Keitaro

机构信息

Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, The University of Tokyo , Shirokanedai 4-6-1, Minato-ku, Tokyo 108-8639, Japan.

Department of General Systems Studies, Graduate School of Arts and Sciences, The University of Tokyo , Komaba 3-8-1, Meguro-ku, Tokyo 153-8902, Japan.

出版信息

ACS Synth Biol. 2017 Dec 15;6(12):2191-2197. doi: 10.1021/acssynbio.7b00246. Epub 2017 Nov 7.

Abstract

Mesenchymal stem cells (MSCs) are of interest in regenerative medicine owing to their multilineage differentiation and self-renewal properties. Understanding the in vivo differentiation process is necessary for clinical applications including cell therapy and transplantation. This remains challenging owing to the lack of induction methods that imitate the natural programming process. Endogenous gene regulation of tissue-specific transcription factors is therefore desirable. In the present study, we demonstrated endogenous activation of adipogenic genes through the dCas9-based transcription system and achieved efficient induction of different types of adipocyte-like cells from MSCs. Interestingly, the MSCs converted via single-gene activation exhibited morphological and molecular properties of white adipocytes, while beige adipocyte-like cells were induced via multiplex gene activation of three specific transcription factors. These results reveal that the fate of MSCs can be effectively manipulated by direct activation of specific endogenous gene expression using a dCas9-based activator with reduced exogenous additives.

摘要

间充质干细胞(MSCs)因其多向分化和自我更新特性而在再生医学领域备受关注。了解其体内分化过程对于包括细胞治疗和移植在内的临床应用至关重要。由于缺乏模仿自然编程过程的诱导方法,这仍然具有挑战性。因此,组织特异性转录因子的内源性基因调控是可取的。在本研究中,我们通过基于dCas9的转录系统证明了脂肪生成基因的内源性激活,并实现了从MSCs高效诱导不同类型的脂肪细胞样细胞。有趣的是,通过单基因激活转化的MSCs表现出白色脂肪细胞的形态和分子特性,而米色脂肪细胞样细胞则通过三种特定转录因子的多重基因激活诱导产生。这些结果表明,使用基于dCas9的激活剂直接激活特定内源性基因表达,并减少外源性添加剂,可以有效地操纵MSCs的命运。

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