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

Author:

Huang Guo N.1,Thatcher Jeffrey E.2,McAnally John1,Kong Yongli3,Qi Xiaoxia1,Tan Wei3,DiMaio J. Michael2,Amatruda James F.134,Gerard Robert D.3,Hill Joseph A.3,Bassel-Duby Rhonda1,Olson Eric N.1

Affiliation:

1. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

2. Department of Cardiovascular and Thoracic Surgery, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

3. Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

4. Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Abstract

Enhancing Heart Function The epicardium, a protective layer of tissue surrounding the mammalian heart, plays a critical role during embryogenesis because it supplies growth factors and multipotent progenitor cells essential for heart development. In adults, the epicardium is dormant but it becomes reactivated when the heart is injured, a response that leads to re-expression of developmental genes. Studying mouse models, Huang et al. (p. 1599 , published online 15 November; see the Perspective by Rosenzweig ) found that the C/EBP transcription factors activated the epicardium during development and injury. Blockade of C/EBP signaling in the epicardium of injured (ischemic) hearts reduced inflammation and improved heart function, a finding that could ultimately lead to new strategies for the repair of heart damage.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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