Akiyama Tomohiko, Wakabayashi Shunichi, Soma Atsumi, Sato Saeko, Nakatake Yuhki, Oda Mayumi, Murakami Miyako, Sakota Miki, Chikazawa-Nohtomi Nana, Ko Shigeru B H, Ko Minoru S H
Department of Systems Medicine, Keio University School of Medicine, Tokyo 160-8582, Japan.
Stem Cells Int. 2017;2017:7215010. doi: 10.1155/2017/7215010. Epub 2017 Apr 9.
Human pluripotent stem cells (hPSCs) have the capacity to differentiate into essentially all cell types in the body. Such differentiation can be directed to specific cell types by appropriate cell culture conditions or overexpressing lineage-defining transcription factors (TFs). Especially, for the activation of myogenic program, early studies have shown the effectiveness of enforced expression of TFs associated with myogenic differentiation, such as PAX7 and MYOD1. However, the efficiency of direct differentiation was rather low, most likely due to chromatin features unique to hPSCs, which hinder the access of TFs to genes involved in muscle differentiation. Indeed, recent studies have demonstrated that ectopic expression of epigenetic-modifying factors such as a histone demethylase and an ATP-dependent remodeling factor significantly enhances myogenic differentiation from hPSCs. In this article, we review the recent progress for in vitro generation of skeletal muscles from hPSCs through forced epigenetic and transcriptional manipulation.
人类多能干细胞(hPSCs)有能力分化为体内几乎所有的细胞类型。通过适当的细胞培养条件或过表达谱系定义转录因子(TFs),这种分化可以导向特定的细胞类型。特别是,对于肌源性程序的激活,早期研究表明,强制表达与肌源性分化相关的转录因子(如PAX7和MYOD1)是有效的。然而,直接分化的效率相当低,这很可能是由于hPSCs特有的染色质特征,它阻碍了转录因子与参与肌肉分化的基因的结合。事实上,最近的研究表明,表观遗传修饰因子(如组蛋白去甲基化酶和ATP依赖性重塑因子)的异位表达显著增强了hPSCs的肌源性分化。在本文中,我们综述了通过强制表观遗传和转录操作从hPSCs体外生成骨骼肌的最新进展。