Heo Hye Jin, Kim Hyoung Kyu, Youm Jae Boum, Cho Sung Woo, Song In-Sung, Lee Sun Young, Ko Tae Hee, Kim Nari, Ko Kyung Soo, Rhee Byoung Doo, Han Jin
National Research Laboratory for Mitochondrial Signaling, Department of Physiology, College of Medicine, Cardiovascular and Metabolic Disease Center, Inje University, Busan, Korea.
Laboratory of Vascular Biology and Stem Cell, Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Exp Mol Med. 2016 Aug 19;48(8):e254. doi: 10.1038/emm.2016.70.
Mitochondria are crucial for maintaining the properties of embryonic stem cells (ESCs) and for regulating their subsequent differentiation into diverse cell lineages, including cardiomyocytes. However, mitochondrial regulators that manage the rate of differentiation or cell fate have been rarely identified. This study aimed to determine the potential mitochondrial factor that controls the differentiation of ESCs into cardiac myocytes. We induced cardiomyocyte differentiation from mouse ESCs (mESCs) and performed microarray assays to assess messenger RNA (mRNA) expression changes at differentiation day 8 (D8) compared with undifferentiated mESCs (D0). Among the differentially expressed genes, Pdp1 expression was significantly decreased (27-fold) on D8 compared to D0, which was accompanied by suppressed mitochondrial indices, including ATP levels, membrane potential, ROS and mitochondrial Ca(2+). Notably, Pdp1 overexpression significantly enhanced the mitochondrial indices and pyruvate dehydrogenase activity and reduced the expression of cardiac differentiation marker mRNA and the cardiac differentiation rate compared to a mock control. In confirmation of this, a knockdown of the Pdp1 gene promoted the expression of cardiac differentiation marker mRNA and the cardiac differentiation rate. In conclusion, our results suggest that mitochondrial PDP1 is a potential regulator that controls cardiac differentiation at an early differentiation stage in ESCs.
线粒体对于维持胚胎干细胞(ESC)的特性以及调节其随后分化为包括心肌细胞在内的多种细胞谱系至关重要。然而,很少有能调控分化速率或细胞命运的线粒体调节因子被鉴定出来。本研究旨在确定控制ESC分化为心肌细胞的潜在线粒体因子。我们从小鼠ESC(mESC)诱导心肌细胞分化,并进行微阵列分析,以评估与未分化的mESC(D0)相比,分化第8天(D8)时信使核糖核酸(mRNA)表达的变化。在差异表达基因中,与D0相比,Pdp1在D8时的表达显著降低(27倍),同时伴随着线粒体指标的抑制,包括ATP水平、膜电位、活性氧和线粒体Ca(2+)。值得注意的是,与模拟对照相比,Pdp1过表达显著增强了线粒体指标和丙酮酸脱氢酶活性,并降低了心脏分化标志物mRNA的表达和心脏分化率。与此一致的是,Pdp1基因敲低促进了心脏分化标志物mRNA的表达和心脏分化率。总之,我们的结果表明线粒体PDP1是一种潜在的调节因子,可在ESC分化早期控制心脏分化。