Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Science. 2012 Dec 21;338(6114):1599-603. doi: 10.1126/science.1229765. Epub 2012 Nov 15.
The epicardium encapsulates the heart and functions as a source of multipotent progenitor cells and paracrine factors essential for cardiac development and repair. Injury of the adult heart results in reactivation of a developmental gene program in the epicardium, but the transcriptional basis of epicardial gene expression has not been delineated. We established a mouse embryonic heart organ culture and gene expression system that facilitated the identification of epicardial enhancers activated during heart development and injury. Epicardial activation of these enhancers depends on a combinatorial transcriptional code centered on CCAAT/enhancer binding protein (C/EBP) transcription factors. Disruption of C/EBP signaling in the adult epicardium reduced injury-induced neutrophil infiltration and improved cardiac function. These findings reveal a transcriptional basis for epicardial activation and heart injury, providing a platform for enhancing cardiac regeneration.
心外膜包裹心脏,并作为多能祖细胞和旁分泌因子的来源,对于心脏发育和修复至关重要。成人心肌损伤会导致心外膜中发育基因程序的重新激活,但心外膜基因表达的转录基础尚未确定。我们建立了一种小鼠胚胎心脏器官培养和基因表达系统,该系统有助于鉴定在心脏发育和损伤过程中心外膜激活的增强子。这些增强子在心外膜中的激活依赖于以 CCAAT/增强子结合蛋白 (C/EBP) 转录因子为核心的组合转录密码。在成年心外膜中破坏 C/EBP 信号会减少损伤诱导的中性粒细胞浸润并改善心脏功能。这些发现揭示了心外膜激活和心脏损伤的转录基础,为增强心脏再生提供了一个平台。