Podocyte injuries exacerbate mesangial proliferative glomerulonephritis

被引:42
作者
Morioka, Y
Koike, H
Ikezumi, Y
Ito, Y
Oyanagi, A
Gejyo, F
Shimizu, F
Kawachi, H
机构
[1] Niigata Univ, Fac Med, Inst Nephrol, Dept Cell Biol, Niigata 9518510, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Div Clin Nephrol & Rheumatol, Niigata, Japan
关键词
puromycin aminonucleoside; anti-Thy 1.1 monoclonal antibody; nephrin; podoplanin;
D O I
10.1046/j.1523-1755.2001.00047.x
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
Background. From the observations of morphology seen in early phases of the experimental models of the irreversible mesangial proliferative glomerulonephritis, we hypothesized that podocyte injury is one of the important factors in bringing upon irreversible glomerular alterations. To verify this hypothesis, we investigated whether podocyte injury induced by puromycin aminonucleoside (PAN) injection affects the mesangial alterations of anti-Thy 1.1 glomerulonephritis. Methods. Female Wistar rats were injected with 0.5 mg monoclonal antibody (mAb) 1-22-3 five days after the injection of 10 mg or 5 mg/100 g body weight (BW) of puromycin aminonucleoside (PAN), and sacrificed at 7 days or 8 weeks after the mAb 1-22-3 injection. Results. Consecutive injections of 10 mg/100 g BW of PAN and mAb 1-22-3 caused the irreversible mesangial alteration with persistent proteinuria (at week 8, proteinuria 100.3 +/- 57.8 mg/24 h, matrix score 1.13 +/- 0.52, collagen type I score 2.04 +/- 0.53, mRNA for collagen type 1227 +/- 79% to the group with a single injection of 1-22-3). Although single injection of 5 mg/100 g BW of PAN was not capable of inducing abnormal proteinuria, consecutive injections of 5 mg/100 g BW of PAN and mAb 1-22-3 also caused irreversible mesangial alteration and persistent proteinuria. Conclusions. Podocyte injury might be an important factor that exacerbates mesangial proliferation and mesangial matrix expansion. The irreversible mesangial alterations caused by consecutive injections of PAN and mAb 1-22-3 may be a novel model that could be used to analyze the mechanism of progressive mesangial alteration.
引用
收藏
页码:2192 / 2204
页数:13
相关论文
共 42 条
[1]   Cloning and expression of the rat nephrin homolog [J].
Ahola, H ;
Wang, SX ;
Luimula, P ;
Solin, ML ;
Holzman, LB ;
Holthöfer, H .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (03) :907-913
[2]   SUPPRESSION OF EXPERIMENTAL GLOMERULONEPHRITIS BY ANTISERUM AGAINST TRANSFORMING GROWTH FACTOR-BETA-1 [J].
BORDER, WA ;
OKUDA, S ;
LANGUINO, LR ;
SPORN, MB ;
RUOSLAHTI, E .
NATURE, 1990, 346 (6282) :371-374
[3]  
BreitenederGeleff S, 1997, AM J PATHOL, V151, P1141
[4]  
CHENG QL, 1995, CLIN EXP IMMUNOL, V102, P181
[5]   A ROLE FOR OXYGEN FREE-RADICALS IN AMINONUCLEOSIDE NEPHROSIS [J].
DIAMOND, JR ;
BONVENTRE, JV ;
KARNOVSKY, MJ .
KIDNEY INTERNATIONAL, 1986, 29 (02) :478-483
[6]  
EDDY AA, 1991, AM J PATHOL, V138, P1111
[7]   INFUSION OF PLATELET-DERIVED GROWTH-FACTOR OR BASIC FIBROBLAST GROWTH-FACTOR INDUCES SELECTIVE GLOMERULAR MESANGIAL CELL-PROLIFERATION AND MATRIX ACCUMULATION IN RATS [J].
FLOEGE, J ;
ENG, E ;
YOUNG, BA ;
ALPERS, CE ;
BARRETT, TB ;
BOWENPOPE, DF ;
JOHNSON, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (06) :2952-2962
[8]  
Floege J, 1998, J AM SOC NEPHROL, V9, P792
[9]   RAT GLOMERULAR MESANGIAL CELLS SYNTHESIZE BASIC FIBROBLAST GROWTH-FACTOR - RELEASE, UP-REGULATED SYNTHESIS, AND MITOGENICITY IN MESANGIAL PROLIFERATIVE GLOMERULONEPHRITIS [J].
FLOEGE, J ;
ENG, E ;
LINDNER, V ;
ALPERS, CE ;
YOUNG, BA ;
REIDY, MA ;
JOHNSON, RJ .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2362-2369
[10]   PODOCALYXIN ON THE GLOMERULAR EPITHELIAL-CELLS IS PRESERVED WELL IN VARIOUS GLOMERULAR-DISEASES [J].
HARA, M ;
YANAGIHARA, T ;
TAKADA, T ;
ITOH, M ;
ADACHI, Y ;
YOSHIZUMI, A ;
KAWASAKI, K ;
YAMAMOTO, T ;
KIHARA, I .
NEPHRON, 1994, 67 (01) :123-124