Acute CD47 Blockade During Ischemic Myocardial Reperfusion Enhances Phagocytosis-Associated Cardiac Repair

Shuang Zhang, Xin Yi Yeap, Matthew DeBerge, Nivedita K. Naresh, Kevin Wang, Zhengxin Jiang, Jane E. Wilcox, Steven M. White, John P. Morrow, Paul W. Burridge, Daniel Procissi, Evan A. Scott, William Frazier, Edward B. Thorp*

*Corresponding author for this work

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

Our data suggest that, after a myocardial infarction, integrin-associated protein CD47 on cardiac myocytes is elevated. In culture, increased CD47 on the surface of dying cardiomyocytes impairs phagocytic removal by immune cell macrophages. After myocardial ischemia and reperfusion, acute CD47 inhibition with blocking antibodies enhanced dead myocyte clearance by cardiac phagocytes and also improved the resolution of cardiac inflammation, reduced infarct size, and preserved cardiac contractile function. Early targeting of CD47 in the myocardium after reperfusion may be a new strategy to enhance wound repair in the ischemic heart.

Original languageEnglish (US)
Pages (from-to)386-397
Number of pages12
JournalJACC: Basic to Translational Science
Volume2
Issue number4
DOIs
StatePublished - Aug 2017

Keywords

  • CD47
  • macrophage
  • phagocytosis

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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