All-trans-retinoic acid inhibits the development of mesangial proliferative glomerulonephritis in interleukin-6 transgenic mice

被引:16
作者
Shima, Y
Iwano, M
Yoshizaki, K
Tanaka, T
Kawase, I
Nishimoto, N
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Lab Immune Regulat, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Med, Dept Mol Med, Osaka, Japan
[3] Nara Med Univ, Dept Internal Med 1, Kashihara, Nara 634, Japan
[4] Osaka Univ, Sch Hlth & Sport Sci, Dept Med Sci 1, Osaka, Japan
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2005年 / 100卷 / 01期
关键词
retinoic acid; mesangial cell; glomerulonephritis; interleukin-6; transgenic mice; vitamin A;
D O I
10.1159/000084655
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
All-trans-retinoic acid ( ATRA), a vitamin A derivative, was reported to suppress the interleukin-6 (IL-6) production and to downregulate the IL-6 receptor (IL-6R) and/or its signal transducer glycoprotein 130. We investigated the in vivo antinephritic effect of ATRA on IL-6 transgenic mice which had developed mesangial proliferative glomerulonephritis (PGN) as well as its in vitro inhibitory effect on the proliferation of rat mesangial cells. In vivo experiments on IL-6 transgenic mice showed that ATRA administration suppressed proteinuria and hematuria and reduced the IL-6 concentrations; furthermore, histological examination demonstrated that it improved PGN. In vitro experiments using rat mesangial cells demonstrated that ATRA inhibited cell growth in a dose-dependent manner within a range from 10(-4) to 10(-6) M. This inhibition by ATRA was partially counteracted by the addition of IL-6. RT-PCR assay results showed that ATRA also reduced IL-6R, but not the glycoprotein 130 expression in mesangial cells. These findings indicate that, by blocking of the IL-6 function, ATRA may be therapeutically effective in PGN. Copyright (C) 2005 S. Karger AG, Basel.
引用
收藏
页码:E54 / E62
页数:9
相关论文
共 32 条
[1]   PRODUCTION OF PLATELET-DERIVED GROWTH FACTORLIKE PROTEIN BY RAT MESANGIAL CELLS IN CULTURE [J].
ABBOUD, HE ;
POPTIC, E ;
DICORLETO, P .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 80 (03) :675-683
[2]   INTERLEUKIN-6 IN BIOLOGY AND MEDICINE [J].
AKIRA, S ;
TAGA, T ;
KISHIMOTO, T .
ADVANCES IN IMMUNOLOGY, VOL 54, 1993, 54 :1-78
[3]   ACUTE ADAPTATIVE CHANGES TO UNILATERAL NEPHRECTOMY IN HUMANS [J].
ARGILES, A ;
MOURAD, G ;
BASSET, N ;
AXELRUDCAVADORE, C ;
HAIECH, J ;
MION, C ;
CAVADORE, JC ;
DEMAILLE, JG .
KIDNEY INTERNATIONAL, 1987, 32 (05) :714-720
[4]  
BRINCKERHOFF CE, 1985, CIBA F SYMP, V113, P191
[5]   1,2-DIOXETANES - NOVEL CHEMI-LUMINESCENT ENZYME SUBSTRATES - APPLICATIONS TO IMMUNOASSAYS [J].
BRONSTEIN, I ;
EDWARDS, B ;
VOYTA, JC .
JOURNAL OF BIOLUMINESCENCE AND CHEMILUMINESCENCE, 1989, 4 (01) :99-111
[6]   RENAL SURVIVAL RATE OF IGA NEPHROPATHY [J].
CHIDA, Y ;
TOMURA, S ;
TAKEUCHI, J .
NEPHRON, 1985, 40 (02) :189-194
[7]   IDIOPATHIC IGA MESANGIAL NEPHROPATHY - CLINICAL AND HISTOLOGICAL STUDY OF 374 PATIENTS [J].
DAMICO, G ;
IMBASCIATI, E ;
DIBELGIOIOSO, GB ;
BERTOLI, S ;
FOGAZZI, G ;
FERRARIO, F ;
FELLIN, G ;
RAGNI, A ;
COLASANTI, G ;
MINETTI, L ;
PONTICELLI, C .
MEDICINE, 1985, 64 (01) :49-60
[8]   Effects of all-trans retinoic acid on renin-angiotensin system in rats with experimental nephritis [J].
Dechow, C ;
Morath, C ;
Peters, J ;
Lehrke, I ;
Waldherr, R ;
Haxsen, V ;
Ritz, E ;
Wagner, J .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2001, 281 (05) :F909-F919
[9]  
DOHI K, 1991, CLIN NEPHROL, V35, P1
[10]   PROGNOSTIC DETERMINANTS IN LUPUS NEPHRITIS - A LONG-TERM CLINICOPATHOLOGICAL STUDY [J].
DONADIO, JV ;
HART, GM ;
BERGSTRALH, EJ ;
HOLLEY, KE .
LUPUS, 1995, 4 (02) :109-115