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SOX10 单一转录因子在人多能干细胞中快速高效产生少突胶质细胞。

SOX10 Single Transcription Factor-Based Fast and Efficient Generation of Oligodendrocytes from Human Pluripotent Stem Cells.

机构信息

Department of Development and Regeneration, Stem Cell Biology and Embryology, KU Leuven Stem Cell Institute, Herestraat 49, Onderwijs en Navorsing 4, Box 804, 3000 Leuven, Belgium.

Department of Development and Regeneration, Stem Cell Biology and Embryology, KU Leuven Stem Cell Institute, Herestraat 49, Onderwijs en Navorsing 4, Box 804, 3000 Leuven, Belgium.

出版信息

Stem Cell Reports. 2018 Feb 13;10(2):655-672. doi: 10.1016/j.stemcr.2017.12.014. Epub 2018 Jan 11.

Abstract

Scarce access to primary samples and lack of efficient protocols to generate oligodendrocytes (OLs) from human pluripotent stem cells (hPSCs) are hampering our understanding of OL biology and the development of novel therapies. Here, we demonstrate that overexpression of the transcription factor SOX10 is sufficient to generate surface antigen O4-positive (O4) and myelin basic protein-positive OLs from hPSCs in only 22 days, including from patients with multiple sclerosis or amyotrophic lateral sclerosis. The SOX10-induced O4 population resembles primary human OLs at the transcriptome level and can myelinate neurons in vivo. Using in vitro OL-neuron co-cultures, myelination of neurons by OLs can also be demonstrated, which can be adapted to a high-throughput screening format to test the response of pro-myelinating drugs. In conclusion, we provide an approach to generate OLs in a very rapid and efficient manner, which can be used for disease modeling, drug discovery efforts, and potentially for therapeutic OL transplantation.

摘要

原发性样本获取困难,且缺乏有效的人多能干细胞(hPSC)向少突胶质细胞(OL)分化的方案,这阻碍了我们对 OL 生物学的理解和新型疗法的开发。在此,我们证明 SOX10 转录因子的过表达足以在短短 22 天内从 hPSC 中产生表面抗原 O4 阳性(O4)和髓鞘碱性蛋白阳性的 OL,其中包括多发性硬化症或肌萎缩性侧索硬化症患者的细胞。SOX10 诱导的 O4 群体在转录组水平上类似于原代人 OL,并可在体内对神经元进行髓鞘化。通过体外 OL-神经元共培养,也可以证明 OL 对神经元的髓鞘化作用,且这种方法可以适应高通量筛选格式,以测试促髓鞘化药物的反应。总之,我们提供了一种快速有效的生成 OL 的方法,可用于疾病建模、药物发现工作,以及潜在的 OL 治疗性移植。

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