Central Research Institute, JW Pharmaceutical Corporation, Hwaseong 445-380, Korea.
Arch Pharm Res. 2012 Nov;35(11):1979-88. doi: 10.1007/s12272-012-1115-6. Epub 2012 Dec 4.
Embryonic stem (ES) cells may be used as an alternative source of functionally intact cardiomyocytes for ischemic heart disease. Several natural and synthetic small molecules have been identified as useful tools for controlling and manipulating stem cell renewal and differentiation. Currently, there is an urgent requirement for novel small molecules that specifically induce differentiation of stem cells into cardiomyocytes. To identify compounds that promote cardiomyogenesis of stem cells, cell-based screening of a peptidomimetic small-molecule library was carried out. A series of β-turn peptidomimetic compounds, including CW209E, increased the expression of α-MHC promoter-driven enhanced green fluorescent protein (EGFP) and ratio of beating embryoid bodies (EBs) without inducing cytotoxicity in mouse embryonic stem cells. CW209E also increased the number of beating EBs in human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs). Thus, this chemical compound should be useful for elucidation of the molecular pathway of cardiogenesis and generation of cardiomyocytes ex vivo, which can be further applied for experimental or clinical cell therapy for ischemic heart diseases.
胚胎干细胞(ES 细胞)可作为治疗缺血性心脏病的功能健全的心肌细胞的替代来源。已经发现了几种天然和合成的小分子,它们可作为控制和操纵干细胞更新和分化的有用工具。目前,迫切需要能够特异性诱导干细胞向心肌细胞分化的新型小分子。为了鉴定促进干细胞心肌发生的化合物,对肽模拟小分子文库进行了基于细胞的筛选。一系列β-转角肽模拟化合物,包括 CW209E,可增加α-MHC 启动子驱动的增强型绿色荧光蛋白(EGFP)的表达和搏动胚状体(EB)的比例,而在小鼠胚胎干细胞中不诱导细胞毒性。CW209E 还增加了人胚胎干细胞(hESC)和人诱导多能干细胞(hiPSC)中搏动 EB 的数量。因此,这种化学化合物应该有助于阐明心肌发生的分子途径,并在体外产生心肌细胞,可进一步应用于缺血性心脏病的实验或临床细胞治疗。