Renal IL-18 production is macrophage independent during obstructive injury

• Published in: PloS one Vol. 7; no. 10; p. e47417
• Main Authors: Franke, Ethan I, Vanderbrink, Brian A, Hile, Karen L, Zhang, Hongji, Cain, Alexandra, Matsui, Futoshi, Meldrum, Kirstan K
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 12.10.2012; Public Library of Science (PLoS)
• Subjects: Acute Kidney Injury - metabolism; Acute Kidney Injury - pathology; Analysis; Animals; Apoptosis; Biology; Bisphosphonates; Body weight; Caspase; Caspase 1 - metabolism; Caspase-1; Clear cell-type renal cell carcinoma; Clodronic acid; Cytokines; Depletion; Enzyme-linked immunosorbent assay; Enzymes; Epithelial cells; Epithelial Cells - cytology; Epithelial Cells - metabolism; Fibroblasts; Fibrosis; Gene expression; Gene Expression Regulation; Genetic aspects; Homogenization; Infiltration; Inflammation; Inflammation - metabolism; Inflammation - pathology; Injuries; Interleukin; Interleukin 18; Interleukin 18 receptors; Interleukin-18 - secretion; Ischemia; Jaundice; Kidney - cytology; Kidney - drug effects; Kidneys; Localization; Macrophages; Macrophages - cytology; Macrophages - metabolism; Male; Medicine; Mice; Receptors, Interleukin-18 - metabolism; Risk factors; Rodents; Signal Transduction; Staining; Surgery; Ureteral Obstruction - metabolism; Ureteral Obstruction - pathology; Urology; Indiana; United States > US; Indianapolis Indiana
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0047417

Interleukin 18 (IL-18) is a pro-inflammatory cytokine that mediates fibrotic renal injury during obstruction. Macrophages are a well-known source of IL-18; however, renal tubular epithelial cells are also a potential source of this cytokine. We hypothesized that IL-18 is predominantly a renal tubular cell product and is produced during renal obstruction independent of macrophage infiltration. To study this, male C57BL6 mice were subjected to unilateral ureteral obstruction (UUO) vs. sham operation in the presence or absence of macrophage depletion (liposomal clodronate (1 ml/100 g body weight i.v.)). The animals were sacrificed 1 week after surgery and renal cortical tissue harvested. Tissue levels of active IL-18 (ELISA), IL-18 receptor mRNA expression (real time PCR), and active caspase-1 expression (western blot) were measured. The cellular localization of IL-18 and IL-18R was assessed using dual labeling immunofluorescent staining (IFS). Immunohistochemical staining of renal tissue sections confirmed macrophage depletion by liposomal clodronate. IL-18 production, IL-18R expression, and active caspase 1 expression were elevated in response to renal obstruction and did not decline to a significant degree in the presence of macrophage depletion. Obstruction-induced IL-18 and IL-18R production localized predominantly to tubular epithelial cells (TEC) during obstruction despite macrophage depletion. These results demonstrate that renal tubular epithelial cells are the primary source of IL-18 production during obstructive injury, and that tubular cell production of IL-18 occurs independent of macrophage infiltration.