Leucine rich α-2 glycoprotein is a potential urinary biomarker for renal tubular injury

被引:30
|
作者
Lee, Hyun [1 ,2 ]
Fujimoto, Minoru [2 ]
Ohkawara, Tomoharu [2 ]
Honda, Hiromi [2 ]
Serada, Satoshi [2 ]
Terada, Yoshio [3 ]
Naka, Tetsuji [2 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
[2] Kochi Univ, Kochi Med Sch, Ctr Intractable Immune Dis, Nanko Ku, Kochi 7838505, Japan
[3] Kochi Univ, Kochi Med Sch, Dept Endocrinol Metab & Nephrol, Nanko Ku, Kochi 7838505, Japan
关键词
LRG; Biomarker; Albumin overload; NLRP3; IL-1; beta; Renal tubular injury; NLRP3 INFLAMMASOME ACTIVATION; PROXIMAL TUBULE; KIDNEY-DISEASE; FIBROSIS; FAILURE; ALPHA(2)-GLYCOPROTEIN; PATHOGENESIS; NEPHROPATHY; PROTEINURIA; PROGRESSION;
D O I
10.1016/j.bbrc.2018.03.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent evidence suggests that renal tubular injury plays a key role in deterioration of renal function in both chronic kidney disease (CKD) and acute kidney injury (AKI). Since commonly used biochemical indicators such as GFR, serum creatinine, blood urea nitrogen and creatinine clearance are inappropriate for detecting alteration in renal tubules, biomarkers reflecting renal tubular injury have been extensively explored. Our research group identified leucine rich alpha-2 glycoprotein (LRG) as a novel serum biomarker for various inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease. In inflammatory diseases, LRG expression is up-regulated at the site of inflammation, in accordance with the induction of LRG in many cell types by various inflammatory cytokines. Recently, urinary LRG was reported as a possible biomarker for several renal diseases, but the mechanism of LRG excretion in urine is still unclear. In this study, by analyzing a mouse albumin (ALB) overload model that is commonly used to study proteinuria-induced renal tubular injury, we provided evidence that urinary LRG is produced in renal tubular epithelial cells by interleukin-1 beta (IL-1 beta) that is released during proteinuria-induced renal damage. In this model, urinary LRG became detectable after ALB overload. In kidney, mRNA expression of LRG together with that of NACHT LRR and PYD domains-containing protein 3 (NLRP3) and IL-1 beta was significantly up-regulated in ALB-overloaded mice, compared to PBS-treated mice. By pathological analysis of kidney, LRG was detected in the injured proximal tubules, distal tubules and collecting ducts in ALB-overloaded mice. Accordingly, in vitro stimulation of mouse renal cortical tubular epithelial cells with excessive ALB led to LRG mRNA up-regulation and its protein secretion, which was effectively blocked by IL-1 receptor antagonist. These results suggest that urinary LRG could be applied to a biomarker detecting renal tubular injury in various renal diseases. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:1045 / 1051
页数:7
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