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1Department of Medicine, Saint Louis University and St. Louis Veterans Affairs Medical Center, St. Louis; 2Departments of Urology and Pathology, New York University School of Medicine, New York, New York; 3Department of Biochemistry, Saint Louis University, St. Louis, Missouri; and 4Department of Medicine, Indiana University, Indianapolis, Indiana
Submitted 17 February 2008 ; accepted in final form 16 May 2008
Tamm-Horsfall protein (THP) is a glycoprotein with unclear functions expressed exclusively in thick ascending limbs (TAL) of the kidney. Its role in ischemic acute kidney injury is uncertain, with previous data suggesting a possible negative effect by enhancing cast formation and promoting inflammation. Using a recently characterized THP knockout mouse (THP–/–), we investigated the role of THP in renal ischemia-reperfusion injury (IRI). In wild-type mice (THP+/+), THP expression was increased by injury. THP–/– mice developed more functional and histological renal damage after IRI compared with THP+/+. THP–/– kidneys showed more inflammation and tubular necrosis. Cast formation correlated with the severity of injury and was independent of THP presence. THP absence was associated with a more necrotic, rather than apoptotic, phenotype of cell death. The outer medulla was predominantly affected, where significant interstitial neutrophil infiltration was detected in proximity to injured S3 proximal tubular segments and TAL. This coincided with an enhanced expression of the innate immunity receptor Toll-like receptor 4 (TLR4) in S3 segments of THP–/– compared with THP+/+ mice. Specifically, a basolateral S3 expression of TLR4 was more evident in THP–/– kidneys compared with a more apical distribution in THP+/+. Such basolateral location for TLR4 allows a greater interaction with proinflammatory ligands present in the interstitium during ischemia. In conclusion, we are showing a completely novel role for a very old protein in the setting of renal injury. Our data suggest that THP stabilizes the outer medulla in the face of injury by decreasing inflammation, possibly through an effect on TLR4.
acute kidney injury; Toll-like receptors; uromodulin; ischemia-reperfusion
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