Phagocyte-myocyte interactions and consequences during hypoxic wound healing

Shuang Zhang, Shirley Dehn, Matthew DeBerge, Ki Jong Rhee, Barry Hudson, Edward B. Thorp

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)


Myocardial infarction (MI), secondary to atherosclerotic plaque rupture and occlusive thrombi, triggers acute margination of inflammatory neutrophils and monocyte phagocyte subsets to the damaged heart, the latter of which may give rise briefly to differentiated macrophage-like or dendritic-like cells. Within the injured myocardium, a primary function of these phagocytic cells is to remove damaged extracellular matrix, necrotic and apoptotic cardiac cells, as well as immune cells that turn over. Recognition of dying cellular targets by phagocytes triggers intracellular signaling, particularly in macrophages, wherein cytokines and lipid mediators are generated to promote inflammation resolution, fibrotic scarring, angiogenesis, and compensatory organ remodeling. These actions cooperate in an effort to preserve myocardial contractility and prevent heart failure. Immune cell function is modulated by local tissue factors that include secreted protease activity, oxidative stress during clinical reperfusion, and hypoxia. Importantly, experimental evidence suggests that monocyte function and phagocytosis efficiency is compromised in the setting of MI risk factors, including hyperlipidemia and ageing, however underlying mechanisms remain unclear. Herein we review seminal phagocyte and cardiac molecular factors that lead to, and culminate in, the recognition and removal of dying injured myocardium, the effects of hypoxia, and their relationship to cardiac infarct size and heart healing.

Original languageEnglish
Pages (from-to)65-73
Number of pages9
JournalCellular Immunology
Issue number1-2
Publication statusPublished - 2014 Sept 1

Bibliographical note

Funding Information:
Funding from NIH 4R00HL097021-03 Grant from the NHLBI (to E.T.).

Publisher Copyright:
© 2014 Elsevier Inc..

All Science Journal Classification (ASJC) codes

  • Immunology


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