Tissue injury, such as occurs in response to a lack of oxygen, promotes an influx of immune cells to the site of damage. After an ischemic injury to the heart, such as occurs after a heart attack or heart transplant, these responses are often maladaptive, resulting in decreased contractility and possible failure. Innate immune cells called neutrophils infiltrate the heart and are linked to pathogenic responses following an ischemic event; however, it is not clear how these cells are recruited to the site of damage.