Glomerular and tubular induction of the transcription factor c-Jun in human renal disease

被引:103
作者
De Borst, M. H.
Prakash, J.
Melenhorst, W. B. W. H.
van den Heuvel, M. C.
Kok, R. J.
Navis, G.
van Goor, H.
机构
[1] Univ Groningen, Dept Pathol & Lab Med, NL-9700 RB Groningen, Netherlands
[2] Univ Med Ctr Groningen, Dept Pathol & Lab Med, NL-9700 RB Groningen, Netherlands
[3] Univ Med Ctr Groningen, Dept Pharmacokinet & Drug Delivery, Groningen, Netherlands
[4] Utrecht Inst Phatrmaceut Sci, Dept Pharmaceut, Utrecht, Netherlands
[5] Univ Groningen, NL-9700 AB Groningen, Netherlands
[6] Univ Med Ctr Groningen, Dept Med, Div Nephrol, Groningen, Netherlands
关键词
c-Jun; activator protein-1 (AP-1); c-Jun N-terminal kinase (JNK); kidney human renal disease; biopsy;
D O I
10.1002/path.2228
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The transcription factor c-Jun regulates the expression of genes involved in proliferation and inflammation in many cell types but its role in human renal disease is largely unclear. In the current study we investigated whether c-Jun activation is associated with human renal disease and if c-Jun activation regulates pro-inflammatory and pro-fibrotic genes in renal cells. Activation of c-Jun was quantified by scoring renal expression of phosphorylated c-Jun (pc-Jun) in control human renal tissue and in biopsies from patients with various renal diseases (diabetic nephropathy, focal glomerulosclerosis, hypertension, IgA nephropathy, membranous glomerulopathy, minimal change disease, membranoproliferative glomerulonephritis, systemic lupus erythematosus, acute rejection, and Wegener's granulomaiosis); this was correlated with parameters of renal damage. Furthermore, we studied the functional role of c-Jun activation in human tubular epithelial cells (HK-2) stimulated with TGF-ss. Activated c-Jun was present in nuclei of glomerular and tubular cells in all human renal diseases, but only sporadically in controls. Across the diseases, the extent of pc-Jun expression correlated with the degree of focal glomerulosclerosis, interstitial fibrosis, cell proliferation, kidney injury molecule-1 (Kim-1) expression, macrophage accumulation, and impairment of renal function. In HK-2 cells,'TGF-ss induced c-Jun activation after 1 h (+40%, p < 0.001) and 24 h (+160%, p < 0.001). The specific c-Jun N-terminal kinase (JNK) inhibitor SP600125 abolished c-Jun phosphorylation at all time points and blunted TGF-ss or BSA-induced procollagen-1 alpha and MCP-1 gene expression in HK-2 cells. We conclude that in human renal disease, the transcription factor c-Jun'is activated in glomerular and tubular cells. Activation of c-Jun may be involved in the regulation of inflammation and/or fibrosis in human renal disease. Copyright (c) 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:219 / 228
页数:10
相关论文
共 36 条
[1]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[2]   PKB and megalin determine the survival or death of renal proximal tubule cells [J].
Caruso-Neves, Celso ;
Pinheiro, Ana Acacia S. ;
Cai, Hui ;
Souza-Menezes, Jackson ;
Guggino, William B. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (49) :18810-18815
[3]   Enalapril reduces the expression of nuclear factor-κB and c-Jun N-terminal kinase in the renal cortices of five-sixths-nephrectomized rats [J].
Costa, Joana C. S. R. ;
Costa, Roberto S. ;
Silva, Cleonice G. A. ;
Coimbra, Terezila M. .
AMERICAN JOURNAL OF NEPHROLOGY, 2006, 26 (03) :281-286
[4]  
DEBORST MH, 2006, SIGNAL TRANSDUCTION, V6, P32
[5]   Chronic inhibition of nuclear factor-κB attenuates renal injury in the 5/6 renal ablation model [J].
Fujihara, Clarice K. ;
Antunes, Glaucia R. ;
Mattar, Ana L. ;
Malheiros, Denise M. A. C. ;
Vieira, Jose M., Jr. ;
Zatz, Roberto .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2007, 292 (01) :F92-F99
[6]   Curcumin blocks multiple sites of the TGF-β signaling cascade in renal cells [J].
Gaedeke, J ;
Noble, NA ;
Border, WA .
KIDNEY INTERNATIONAL, 2004, 66 (01) :112-120
[7]  
Grandaliano G, 1996, J AM SOC NEPHROL, V7, P906
[8]   Kidney Injury Molecule-1 (KIM-1): A novel biomarker for human renal proximal tubule injury [J].
Han, WK ;
Bailly, V ;
Abichandani, R ;
Thadhani, R ;
Bonventre, JV .
KIDNEY INTERNATIONAL, 2002, 62 (01) :237-244
[9]  
Han ZN, 2001, J CLIN INVEST, V108, P73, DOI 10.1172/JCI12466
[10]   Priming of glomerular mesangial cells by activated macrophages causes blunted responses to proinflammatory stimuli [J].
Hayakawa, K ;
Meng, YM ;
Hiramatsu, N ;
Kasai, A ;
Yamauchi, K ;
Yao, J ;
Kitamura, M .
JOURNAL OF IMMUNOLOGY, 2006, 176 (04) :2529-2537