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C/EBP Transcription Factors Mediate Epicardial Activation During Heart Development and Injury
Author(s) -
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 BasselDuby,
Eric N. Olson
Publication year - 2012
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.1229765
Subject(s) - heart development , transcription factor , inflammation , blockade , microbiology and biotechnology , progenitor cell , biology , medicine , cardiology , stem cell , receptor , gene , embryonic stem cell , genetics
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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