Expression of glomerular plasminogen activator inhibitor type 1 in glomerulonephritis

被引:63
作者
Hamano, K
Iwano, M
Akai, Y
Sato, H
Kubo, A
Nishitani, Y
Uyama, H
Yoshida, Y
Miyazaki, M
Shiiki, H
Kohno, S
Dohi, K
机构
[1] Nara Med Univ, Dept Internal Med 1, Kashihara, Nara 6348522, Japan
[2] Nagasaki Univ, Sch Med, Dept Internal Med 2, Nagasaki 852, Japan
关键词
plasminogen activator inhibitor type 1 (PAI-1); tissue plasminogen activator (tPA); focal segmental; glomerulosclerosis (FSGS); membranous nephropathy (MN);
D O I
10.1053/ajkd.2002.31986
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
Plasminogen activator inhibitor type 1 (PAI-1) and tissue plasminogen activator (tPA) are the major regulators of plasmin generation. Glomerular PAI-1/tPA balance is involved in extracellular matrix turnover, as well as fibrin deposition in glomerull. Renal biopsy specimens were obtained from 80 patients with either primary or secondary glomerulonephritis (10 patients, minimal change nephrotic syndrome; 6 patients, focal segmental glomerulosclerosis [FSGS]; 10 patients, membranous nephropathy [MN]; 24 patients, mesangial proliferative glomerulonephritis; 15 patients, lupus nephritis; 14 patients, diabetic nephropathy; and I patient, membranoproliferative glomerulonephritis). We quantified glomerular PAI-1 and tPA messenger RNA (mRNA) by competitive polymerase chain reaction. We also determined PAI-1 mRNA localization by In situ hybridization. Glomerular PAI-1 mRNA levels in patients with FSGS and MN were significantly greater than those of controls. There was a sixfold increase in PAI-1-tPA mRNA ratio in patients with MN compared with the control group. In addition, glomerular PAI-1 mRNA level correlated with level of proteinuria. Conversely, there was no difference in tPA mRNA levels among types of glomerulonephritis. These results suggest that suppressed glomerular fibrinolytic and proteolytic activity may be associated with the pathogenesis of glomerulonephritis, especially in FSGS and MN. (C) 2002 by the National Kidney Foundation, Inc.
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收藏
页码:695 / 705
页数:11
相关论文
共 55 条
[1]   Expression of decay accelerating factor mRNA and complement C3 mRNA in human diseased kidney [J].
Abe, K ;
Miyazaki, M ;
Koji, T ;
Furusu, A ;
Ozono, Y ;
Harada, T ;
Sakai, H ;
Nakane, PK ;
Kohno, S .
KIDNEY INTERNATIONAL, 1998, 54 (01) :120-130
[2]   TISSUE-TYPE PLASMINOGEN-ACTIVATOR AND ITS INHIBITOR IN HUMAN GLOMERULONEPHRITIS [J].
AYA, N ;
YOSHIOKA, K ;
MURAKAMI, K ;
HINO, S ;
OKADA, K ;
MATSUO, O ;
MAKI, S .
JOURNAL OF PATHOLOGY, 1992, 166 (03) :289-295
[3]   EARLY-SEASON EFFECTS OF SUPPLEMENTED SOLAR UV-B RADIATION ON SEEDLING EMERGENCE, CANOPY STRUCTURE, SIMULATED STAND PHOTOSYNTHESIS AND COMPETITION FOR LIGHT [J].
BARNES, PW ;
FLINT, SD ;
CALDWELL, MM .
GLOBAL CHANGE BIOLOGY, 1995, 1 (01) :43-53
[4]   ANALYSIS OF THE PLASMINOGEN-ACTIVATOR ACTIVITY OF THE HUMAN GLOMERULUS [J].
BERGSTEIN, JM ;
RILEY, M ;
BANG, NU .
KIDNEY INTERNATIONAL, 1988, 33 (04) :868-874
[5]   GLOMERULAR FIBRIN DEPOSITION AND REMOVAL [J].
BERGSTEIN, JM .
PEDIATRIC NEPHROLOGY, 1990, 4 (01) :78-87
[6]  
Cai Y, 1996, J PATHOL, V179, P188
[7]  
COLLEN D, 1980, THROMB HAEMOSTASIS, V43, P77
[8]   PLASMINOGEN ACTIVATORS, TISSUE DEGRADATION, AND CANCER [J].
DANO, K ;
ANDREASEN, PA ;
GRONDAHLHANSEN, J ;
KRISTENSEN, P ;
NIELSEN, LS ;
SKRIVER, L .
ADVANCES IN CANCER RESEARCH, 1985, 44 :139-266
[9]  
DAWSON SJ, 1993, J BIOL CHEM, V268, P10739
[10]   Bleomycin-induced pulmonary fibrosis in transgenic mice that either lack or overexpress the murine plasminogen activator inhibitor-1 gene [J].
Eitzman, DT ;
McCoy, RD ;
Zheng, XX ;
Fay, WP ;
Shen, TL ;
Ginsburg, D ;
Simon, RH .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (01) :232-237