화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.364, No.3, 502-508, 2007
Involvement of glomerular SREBP-1c in diabetic nephropathy
The role of glomerular SREBP-1c in diabetic nephropathy was investigated. PEPCK-promoter transgenic mice overexpressing nuclear SREBP-1c exhibited enhancement of proteinuria with mesangial proliferation and matrix accumulation, mimicking diabetic nephropathy, despite the absence of hyperglycemia or hyperlipidemia. Isolated transgenic glomeruli had higher expression of TGF beta-1, fibronectin, and SPARC in the absence of marked lipid accumulation. Gene expression of P47(phox), p67(phox), and PU.1 were also activated, accompanying increased 8-OHdG in urine and kidney, demonstrating that glomerular SREBP-1c could directly cause oxidative stress through induced NADPH oxidase. Similar changes were observed in STZ-treated diabetic mice with activation of endogenous SREBP-1c. Finally, diabetic proteinuria and oxidative stress were ameliorated in SREBP-1-null mice. Adenoviral overexpression of active and dominant-negative SREBP-I c caused consistent reciprocal changes in expression of both profibrotic and oxidative stress genes in MESI3 mesangial cells. These data suggest that activation of glomerular SREBP-1c could contribute to emergence and/or progression of diabetic nephropathy. (C) 2007 Elsevier Inc. All rights reserved.