4.8 Article

C/EBP Transcription Factors Mediate Epicardial Activation During Heart Development and Injury

Journal

SCIENCE
Volume 338, Issue 6114, Pages 1599-1603

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1229765

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Funding

  1. O'Donnell Foundation Fellow of the Life Sciences Research Foundation
  2. NIH Pathway [1K99HL114738]
  3. NIH [HL100401-01]
  4. Donald W. Reynolds Center for Clinical Cardiovascular Research
  5. American Heart Association
  6. Jon Holden DeHaan Foundation
  7. Leducq Foundation
  8. Robert A. Welch Foundation [1-0025]

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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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