Expression of renal transforming growth factor-β and its receptors in a rat model of chronic cyclosporine-induced nephropathy

被引:10
作者
Bing, P. [1 ]
Maode, L. [1 ]
Li, F. [1 ]
Sheng, H. [1 ]
机构
[1] Sichuan Univ, W China Hosp, Dept Surg, Chengdu 610041, Peoples R China
关键词
TUBULAR EXPRESSION; FACTOR-BETA(1); GROWTH-FACTOR-BETA-1; STIMULATION; DYSFUNCTION;
D O I
10.1016/j.transproceed.2006.07.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective. We sought to detect expression of transforming growth factor-beta 1 (TGF-beta 1) as well as its receptors type I (TRI) and type II (TRII) in rat kidneys during chronic cyclosporine (CsA)-induced nephropathy. Methods. Twenty four rats were randomly divided into three experimental groups: group 1; NSD (control, n = 8) were administered a normal sodium diet, group 2; LSD (n = 8) were administered a low sodium diet, group 3; CsA (n = 8) were sodium-depleted rats administered Neoral by gastric gavage in a model of chronic CsA-induced nephropathy. TGF-beta 1, TRI, and TRII proteins, as well as TRI and TRII mRNAs were measured in the CsA-treated rat kidneys by immunohistochemistry and in situ hybridization, respectively. Serniquantitative results were shown by image analysis. Results. The expression of TGF-beta 1, TRI, TRII, TRI mRNA, and TRII mRNA were all increased in CsA-treated rat kidneys, compared with NSD or LSD (P < .05). Conclusion. Our study showed that the ligand of TGF-beta 1 and its receptors TRI, TRII were all up-regulated. It may be important inhibit the expression of TGF-beta 1 or its receptors in patients who suffer from chronic CsA-induced nephropathy.
引用
收藏
页码:2176 / 2179
页数:4
相关论文
共 11 条
[1]   REGULATION OF TRANSFORMING GROWTH FACTOR-BETA(1) AND ITS RECEPTOR BY CYCLOSPORINE IN HUMAN T-LYMPHOCYTES [J].
AHUJA, SS ;
SHRIVASTAV, S ;
DANIELPOUR, D ;
BALOW, JE ;
BOUMPAS, DT .
TRANSPLANTATION, 1995, 60 (07) :718-723
[2]  
Hong SW, 2001, AM J PATHOL, V158, P1653
[3]  
Jiang Wei, 2002, Zhonghua Yi Xue Za Zhi, V82, P1160
[4]   In vivo hyperexpression of transforming growth factor-beta(1) in mice: Stimulation by cyclosporine [J].
Khanna, A ;
Kapur, S ;
Sharma, V ;
Li, BG ;
Suthanthiran, M .
TRANSPLANTATION, 1997, 63 (07) :1037-1039
[5]   Increased renal tubular expression of transforming growth factor beta in human allografts correlates with cyclosporine toxicity [J].
Pankewycz, OG ;
Miao, L ;
Isaacs, R ;
Guan, J ;
Pruett, T ;
Haussmann, G ;
Sturgill, BC .
KIDNEY INTERNATIONAL, 1996, 50 (05) :1634-1640
[6]   Blockade of type β transforming growth factor signaling prevents liver fibrosis and dysfunction in the rat [J].
Qi, Z ;
Atsuchi, N ;
Ooshima, A ;
Takeshita, A ;
Ueno, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :2345-2349
[7]   TGF-β receptor expression and binding in rat mesangial cells:: Modulation by glucose and cyclic mechanical strain [J].
Riser, BL ;
Ladson-Wofford, S ;
Sharba, A ;
Cortes, P ;
Drake, K ;
Guerin, CJ ;
Yee, J ;
Choi, ME ;
Segarini, PR ;
Narins, RG .
KIDNEY INTERNATIONAL, 1999, 56 (02) :428-439
[8]  
SHANKLAND SJ, 1996, KIDNEY INT, V49, P430
[9]   Role of transforming growth factor-beta 1 in experimental chronic cyclosporine nephropathy [J].
Shihab, FS ;
Andoh, TF ;
Tanner, AM ;
Noble, NA ;
Border, WA ;
Franceschini, N ;
Bennett, WM .
KIDNEY INTERNATIONAL, 1996, 49 (04) :1141-1151
[10]   In vivo expression of transforming growth factor-β1 in humans -: Stimulation by cyclosporine [J].
Shin, GT ;
Khanna, A ;
Ding, RC ;
Sharma, VK ;
Lagman, M ;
Li, BG ;
Suthanthiran, M .
TRANSPLANTATION, 1998, 65 (03) :313-318