Effects of advanced glycosylation endproducts on perlecan core protein of glomerular epithelium

被引:30
作者
Ha, TS
Song, CJ
Lee, JH
机构
[1] Chungbuk Natl Univ, Coll Med, Dept Pediat, Cheongju 361240, South Korea
[2] Pochon CHA Univ, Coll Med, Dept Pediat, Sungnam, South Korea
关键词
diabetic nephropathy; advanced glycosylation end-products; heparan sulfate proteoglycan; kidney glomerulus; epithelial cells;
D O I
10.1007/s00467-004-1590-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Perlecan is one of major heparan sulfate proteoglycans in the glomerular basement membrane and is reduced in the renal parenchyma of diabetic patients and animals with proteinuria. To examine the effects of glucose and advanced glycosylated end-products (AGE) on perlecan, we cultured rat glomerular epithelial cells (GEpC) on AGE- or bovine serum albumin (BSA)-coated plates under normal (NG, 5 mM) and high-glucose (HG, 30 mM) conditions and measured the change in perlecan core protein production by a sandwich ELISA and northern blot analysis. We observed significant decreases of perlecan core protein under HG conditions at 1 week incubation, specifically on the AGE-coated compared with the BSA-coated surface, by 22.2% and 4.7%, respectively. The expression of mRNA for perlecan promoter was decreased under HG conditions on AGE-coated surfaces by 19.7% at 2 days and 61.1% at 1 week. Even under NG condition, the expression of mRNA was reduced by 30% at 1 week if GEpC were grown on an AGE-coated surface. In conclusion, HG and AGE have an additive effect in reducing the production of perlecan core protein by GEpC in vitro. AGE had a greater effect than HG, implying that the inhibition of AGE formation may be more effective than short-term glucose control in the prevention of diabetic proteinuria.
引用
收藏
页码:1219 / 1224
页数:6
相关论文
共 32 条
[1]  
BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
[2]   ECM GENE-EXPRESSION AND ITS MODULATION BY INSULIN IN DIABETIC RATS [J].
FUKUI, M ;
NAKAMURA, T ;
EBIHARA, I ;
SHIRATO, I ;
TOMINO, Y ;
KOIDE, H .
DIABETES, 1992, 41 (12) :1520-1527
[3]   Regulation of glomerular endothelial cell proteoglycans by glucose [J].
Ha, TS ;
Duraisamy, S ;
Faulkner, JL ;
Kasinath, BS .
JOURNAL OF KOREAN MEDICAL SCIENCE, 2004, 19 (02) :245-252
[4]  
Ha TS, 1999, J AM SOC NEPHROL, V10, P1931
[5]   THE BIOLOGY OF PERLECAN - THE MULTIFACETED HEPARAN-SULFATE PROTEOGLYCAN OF BASEMENT-MEMBRANES AND PERICELLULAR MATRICES [J].
IOZZO, RV ;
COHEN, IR ;
GRASSEL, S ;
MURDOCH, AD .
BIOCHEMICAL JOURNAL, 1994, 302 :625-639
[6]   Early increase of chondroitin sulfate glycosaminoglycan in the glomerular basement membrane of rats with diabetic glomerulopathy [J].
Karasawa, R ;
Nishi, S ;
Suzuki, Y ;
Imai, N ;
Arakawa, M .
NEPHRON, 1997, 76 (01) :62-71
[7]  
Kasinath BS, 1996, J CELL PHYSIOL, V167, P131, DOI 10.1002/(SICI)1097-4652(199604)167:1<131::AID-JCP15>3.3.CO
[8]  
2-O
[9]   DIABETES-MELLITUS INDUCED-INHIBITION OF GLUCOSAMINYL N-DEACETYLASE - EFFECT OF SHORT-TERM BLOOD-GLUCOSE CONTROL IN DIABETIC RATS [J].
KOFOEDENEVOLDSEN, A ;
NOONAN, D ;
DECKERT, T .
DIABETOLOGIA, 1993, 36 (04) :310-315
[10]   ISOLATION AND CHARACTERIZATION OF RAT GLOMERULAR EPITHELIAL-CELLS INVITRO [J].
KREISBERG, JI ;
HOOVER, RL ;
KARNOVSKY, MJ .
KIDNEY INTERNATIONAL, 1978, 14 (01) :21-30