[PDF][PDF] Tissue-specific macrophage responses to remote injury impact the outcome of subsequent local immune challenge

FF Hoyer, K Naxerova, MJ Schloss, M Hulsmans… - Immunity, 2019 - cell.com
FF Hoyer, K Naxerova, MJ Schloss, M Hulsmans, AV Nair, P Dutta, DM Calcagno
Immunity, 2019cell.com
Myocardial infarction, stroke, and sepsis trigger systemic inflammation and organism-wide
complications that are difficult to manage. Here, we examined the contribution of
macrophages residing in vital organs to the systemic response after these injuries. We
generated a comprehensive catalog of changes in macrophage number, origin, and gene
expression in the heart, brain, liver, kidney, and lung of mice with myocardial infarction,
stroke, or sepsis. Predominantly fueled by heightened local proliferation, tissue macrophage …
Summary
Myocardial infarction, stroke, and sepsis trigger systemic inflammation and organism-wide complications that are difficult to manage. Here, we examined the contribution of macrophages residing in vital organs to the systemic response after these injuries. We generated a comprehensive catalog of changes in macrophage number, origin, and gene expression in the heart, brain, liver, kidney, and lung of mice with myocardial infarction, stroke, or sepsis. Predominantly fueled by heightened local proliferation, tissue macrophage numbers increased systemically. Macrophages in the same organ responded similarly to different injuries by altering expression of tissue-specific gene sets. Preceding myocardial infarction improved survival of subsequent pneumonia due to enhanced bacterial clearance, which was caused by IFNɣ priming of alveolar macrophages. Conversely, EGF receptor signaling in macrophages exacerbated inflammatory lung injury. Our data suggest that local injury activates macrophages in remote organs and that targeting macrophages could improve resilience against systemic complications following myocardial infarction, stroke, and sepsis.
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