Expression of osteopontin in cisplatin-induced tubular injury

被引:15
作者
Iguchi, S
Nishi, S
Ikegame, M
Hoshi, K
Yoshizawa, T
Kawashima, H
Arakawa, M
Ozawa, H
Gejyo, F
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Div Clin Nephrol & Rheumatol, Niigata 9518510, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Div Anat & Cell Biol Hard Tissue Tissue Regenerat, Niigata, Japan
[3] Niigata Univ, Grad Sch Med & Dent Sci, Div Cell Biol & Mol Pharmacol Tissue Regenerat &, Course Oral Life Sci, Niigata, Japan
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2004年 / 97卷 / 03期
关键词
osteopontin; cisplatin; tubular injury;
D O I
10.1159/000078643
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Osteopontin (OPN) is considered as a key protein in cell regeneration. OPN is thought to have many functions in cell-cell binding and cell-matrix binding via OPN receptors in various organs. But there is little information on the precise role of OPN. To clarify the functional role of OPN in tubular injury, we performed in situ hybridization and immunohistochemical analysis of the expression of OPN in a renal cortical necrosis model induced by cisplatin from the acute injury to late recovery phases. In the acute injury phase, both mRNA and protein of OPN were markedly induced in damaged tubular lumens with cell debris. In the late recovery phase, on the other hand, OPN protein and mRNA were observed in dilated and flattened tubular epithelial cells showing a regenerative appearance. Most of these cells were also immunostained with CD44, a receptor of OPN. PCNA staining was also co-localized with these expressions. In light of the CD44 function regulating cell proliferation, these findings suggest that OPN may contribute to regeneration of tubular epithelial cells during the acute to late recovery phases of cortical tubular damage induced by cisplatin. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:96 / 105
页数:10
相关论文
共 21 条
[11]   In vivo targeting of inducible NO synthase with oligodeoxynucleotides protects rat kidney against ischemia [J].
Noiri, E ;
Peresleni, T ;
Miller, F ;
Goligorsky, MS .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (10) :2377-2383
[12]   Characterization of CD44-mediated hyaluronan binding by renal tubular epithelial cells [J].
Oertli, B ;
Fan, XH ;
Wuthrich, RP .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1998, 13 (02) :271-278
[13]   Role of intrinsic renal cells versus infiltrating cells in glomerular crescent formation [J].
Ophascharoensuk, V ;
Pippin, JW ;
Gordon, KL ;
Shankland, SJ ;
Couser, WG ;
Johnson, RJ .
KIDNEY INTERNATIONAL, 1998, 54 (02) :416-425
[14]   Differences in osteopontin up-regulation between proximal and distal tubules after renal ischemia/reperfusion [J].
Persy, VP ;
Verstrepen, WA ;
Ysebaert, DK ;
De Greef, KE ;
De Broe, ME .
KIDNEY INTERNATIONAL, 1999, 56 (02) :601-611
[15]  
PICHLER R, 1994, AM J PATHOL, V144, P915
[16]  
PRINCE CW, 1987, J BIOL CHEM, V262, P2900
[17]   Osteopontin inhibits nitric oxide production and cytotoxicity by activated RAW264.7 macrophages [J].
Rollo, EE ;
Laskin, DL ;
Denhardt, DT .
JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (03) :397-404
[18]   Differential effects of osteopontin on the cytotoxic activity of macrophages from young and old mice [J].
Rollo, EE ;
Denhardt, DT .
IMMUNOLOGY, 1996, 88 (04) :642-647
[19]   OSTEOPONTIN MESSENGER-RNA IN THE KIDNEY ON AN EXPERIMENTAL RAT MODEL OF RENAL STONE FORMATION WITHOUT RENAL-FAILURE [J].
UMEKAWA, T ;
YAMATE, T ;
AMASAKI, N ;
KOHRI, K ;
KURITA, T .
UROLOGIA INTERNATIONALIS, 1995, 55 (01) :6-10
[20]   Receptor-ligand interaction between CD44 and osteopontin (Eta-1) [J].
Weber, GF ;
Ashkar, S ;
Glimcher, MJ ;
Cantor, H .
SCIENCE, 1996, 271 (5248) :509-512