The lectin like domain of thrombomodulin is involved in the defence against pyelonephritis. Issue 6 (December 2015)

• Record Type: Journal Article
• Authors: Lattenist, Lionel; Teske, Gwendoline; Claessen, Nike; Florquin, Sandrine; Conway, Edward M.; Roelofs, Joris J.T.H.
• Is Part Of: Thrombosis research. Volume 136:Issue 6(2015)
• Page Start: 1325
• Page End: 1331
• Publication Date: 2015-12
• Subjects: Thrombosis -- Periodicals; 616.135
• DOI: 10.1016/j.thromres.2015.11.004
• Languages: English
• ISSNs: 0049-3848

Abstract

Abstract: Pyelonephritis, a common complication of urinary tract infections, is frequently associated with kidney scarring and may lead to end-stage renal disease. During bacterial infections inflammatory and coagulation pathways and their mutual interaction are playing pivotal roles in the host response. Given that thrombomodulin (TM) is crucially involved in the interplay between coagulation and inflammation, we aimed to investigate the roles of its EGF and lectin-like domains in inflammation during acute pyelonephritis. Indeed, the EGF-like and the lectin-like domains of TM, are especially known to orchestrate inflammation and coagulation in different ways. Acute pyelonephritis was induced by intravesical inoculation of 1 × 10 8 CFU of uropathogenic Escherichia coli in two strains of TM transgenic mice. TM pro/pro mice carry a mutation in the EGF-like domain making them unable to activate protein C, an anticoagulant and anti-inflammatory protein. TM LeD/LeD mice lack the lectin-like domain of TM, which is critical for its anti-inflammatory and cytoprotective properties. Mice were sacrificed 24 and 48 h after inoculation. Bacterial loads, the immune response and the activation of coagulation were evaluated in the kidney and the bladder. TM LeD/LeD mice showed elevated bacterial load in bladder and kidneys compared to WT mice, whereas TM pro/pro had similar bacterial load as WT mice. TM LeD/LeD mice displayed a reduced local production of pro-inflammatory cytokines and neutrophil renal infiltration. Activation of coagulation was comparable in TM LeD/LeD and WT mice. From these data, we conclude that the lectin-like domain of thrombomodulin is critically involved in host defence against E. coli induced acute pyelonephritis. Highlights: Mice lacking the lectin-like domain of thrombomodulin (TM LeD/LeD mice) show elevated bacterial load in bladder and kidneys. TM LeD/LeD mice display reduced local production of pro-inflammatory cytokines and neutrophil renal infiltration. The lectin-like domain of thrombomodulin is critically involved in host defence against E. coli induced acute pyelonephritis.