Endogenous danger signals released from necrotic cells are thought to be sensed by phagocytes leading to secretion of IL-1α and neutrophilic recruitment. However, the mechanisms for IL-1α production and IL-1α-mediated sterile inflammation remain poorly understood. We report here that necrotic cell extracts elicited little secretion of CXCL1 and IL-6 from macrophages but robust production in mesothelial cells. The induction of CXCL1 as well as activation of NF-κB and MAPKs by cytosolic extracts required the presence of IL-1α in the necrotic cell. Conversely, expression of IL-1R and MyD88 but not IL-1α, RICK, TLR2, TLR4, TRIF, or inflammasome components in mesothelial cells was critical for the production of CXCL1. Furthermore, IL-1α was critical to induce the recruitment of neutrophils in the peritoneal cavity via CXCR2. These studies show that IL-1α is a key danger signal released from necrotic cells to trigger CXCL1 secretion and recruitment of neutrophils via IL-1R/MyD88 on neighboring mesothelial cells.
CITATION STYLE
Eigenbrod, T., Park, J.-H., Harder, J., Iwakura, Y., & Núñez, G. (2008). Cutting Edge: Critical Role for Mesothelial Cells in Necrosis-Induced Inflammation through the Recognition of IL-1α Released from Dying Cells. The Journal of Immunology, 181(12), 8194–8198. https://doi.org/10.4049/jimmunol.181.12.8194
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