心脏发育
转录因子
炎症
封锁
细胞生物学
祖细胞
生物
医学
内科学
心脏病学
干细胞
受体
基因
胚胎干细胞
遗传学
作者
Guo N. Huang,Jeffrey E. Thatcher,John McAnally,Yongli Kong,Xiaoxia Qi,Wei Tan,J. Michael DiMaio,James F. Amatruda,Robert D. Gerard,Joseph A. Hill,Rhonda Bassel‐Duby,Eric N. Olson
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-11-17
卷期号:338 (6114): 1599-1603
被引量:213
标识
DOI:10.1126/science.1229765
摘要
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.
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