Renal osteopontin protein and mRNA upregulation during acute nephrotoxicity in the rat

被引:30
作者
Verstrepen, WA [1 ]
Persy, VP [1 ]
Verhulst, A [1 ]
Dauwe, S [1 ]
De Broe, ME [1 ]
机构
[1] Univ Antwerp, Dept Nephrol Hypertens, B-2650 Edegem, Belgium
关键词
acute renal failure; gentamicin; kidney; mercuric chloride;
D O I
10.1093/ndt/16.4.712
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. The effect of segment-specific proximal tubular injury on spatio-temporal osteopontin (OPN) distribution was determined in two different nephrotoxic rat models to evaluate its conceivability with a possible role for OPN in acute renal failure (ARF). OPN gene expression was further determined in proximal and distal tubular cells to investigate the origin of increased renal OPN. Methods. Renal OPN protein and mRNA expression were compared in the rat during mercuric-chloride- vs gentamicin-induced ARF using immunohistochemistry and ill situ hybridization. Results. Mercuric chloride primarily induced tubular injury and subsequent cell proliferation in proximal straight tubules (PST), whereas gentamicin predominantly injured proximal convoluted tubules (PCT). In both models, the distribution of OPN protein was associated with increased OPN mRNA levels in proximal as well as distal tubular cells. However, upregulation was delayed in the proximal tubular segment suffering most from injury, i.e. PCT in gentamicin ARF vs PST in mercuric-chloride ARF. OPN immunostaining at the apical cell membrane from distal tubules was in contrast to perinuclear vesicular staining in proximal tubular cells. Conclusions. OPN gene and protein expression is induced in both proximal and distal tubular cells during rat toxic ARF. The distinct subcellular localization in proximal vs distal tubular cells indicates differences in OPN processing and/or handling. The spatiotemporal distribution is consistent with a possible role ill renal injury and regeneration.
引用
收藏
页码:712 / 724
页数:13
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