Abstract
Following myocardial infarction (MI), circulating blood monocytes respond to chemotactic factors, migrate into the infarcted myocardium, and differentiate into macrophages. At the injury site, macrophages remove necrotic cardiac myocytes and apoptotic neutrophils; secrete cytokines, chemokines, and growth factors; and modulate phases of the angiogenic response. As such, the macrophage is a primary responder cell type that is involved in the regulation of post-MI wound healing at multiple levels. This review summarizes what is currently known about macrophage functions post-MI and borrows literature from other injury and inflammatory models to speculate on additional roles. Basic science and clinical avenues that remain to be explored are also discussed.
Original language | English (US) |
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Pages (from-to) | 147-158 |
Number of pages | 12 |
Journal | International Journal of Cardiology |
Volume | 130 |
Issue number | 2 |
DOIs | |
State | Published - Nov 12 2008 |
Externally published | Yes |
Keywords
- Angiogenesis
- Fibrosis
- Left ventricular remodeling
- Macrophage
- Matrix metalloproteinases
- Myocardial infarction
ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine