TY - JOUR
T1 - Glomerular and tubular induction of the transcription factor c-Jun in human renal disease
AU - de Borst, M. H.
AU - Prakash, J.
AU - Melenhorst, W. B. W. H.
AU - van den Heuvel, M. C.
AU - Kok, R. J.
AU - Navis, G.
AU - van Goor, H.
N1 - Proceedings Paper 6
PY - 2007/10
Y1 - 2007/10
N2 - 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.
AB - 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.
KW - c-Jun
KW - activator protein-1 (AP-1)
KW - c-Jun N-terminal kinase (JNK)
KW - kidney human renal disease
KW - biopsy
KW - NF-KAPPA-B
KW - MONOCYTE CHEMOATTRACTANT PROTEIN-1
KW - HUMAN ENDOTHELIAL-CELLS
KW - TERMINAL KINASE
KW - RESPONSE ELEMENTS
KW - AP-1 ACTIVATION
KW - GENE-EXPRESSION
KW - MESANGIAL CELLS
KW - GLOMERULONEPHRITIS
KW - INJURY
U2 - 10.1002/path.2228
DO - 10.1002/path.2228
M3 - Article
VL - 213
SP - 219
EP - 228
JO - JOURNAL OF PATHOLOGY
JF - JOURNAL OF PATHOLOGY
SN - 0022-3417
IS - 2
T2 - 39th Annual Meeting of the American-Society-of-Nephrology
Y2 - 14 November 2006 through 19 November 2006
ER -