High glucose-induced TGF-beta 1 regulates mesangial production of heparan sulfate proteoglycan

被引:62
作者
Kolm, V [1 ]
Sauer, U [1 ]
Olgemoller, B [1 ]
Schleicher, ED [1 ]
机构
[1] UNIV MUNICH, ACAD HOSP, DIABET RES INST, DEPT BIOCHEM, D-80804 MUNICH, GERMANY
来源
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY | 1996年 / 270卷 / 05期
关键词
diabetic nephropathy; transforming growth factor-beta 1 antisense; perlecan; fibronectin; hyperglycemia;
D O I
10.1152/ajprenal.1996.270.5.F812
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Previous investigations have demonstrated that growing mesangial cells in high glucose concentration stimulates extracellular matrix synthesis and also increases the expression of transforming growth factor-beta (TGF-beta). We examined the effects of hyperglycemia on mesangial proliferation and heparan sulfate proteoglycan (HSPG) and fibronectin production. Prolonged exposure of mesangial cells to increasing glucose concentrations resulted in dose-dependent effects on growth inhibition and stimulation of matrix production. Treatment of mesangial cells with high glucose-conditioned medium or with TGF-beta 1 mimicked the effects of high-glucose incubation. Furthermore, TGF-beta 1 caused a dose-dependent increase in HSPG mRNA levels. The high-glucose effects on mesangial cells were preceded by an increase in total TGF-beta 1 protein. The presence of TGF-beta 1 antisense oligonucleotide attenuated the glucose-mediated effects on mesangial proliferation and matrix production. The data show that even moderately elevated glucose concentrations appear to affect the mesangial cells. The results indicate that 1) TGF-beta 1 protein production is necessary to obtain the high glucose-induced effects and 2) TGF-beta 1 stimulates mesangial HSPG expression and production. Because these effects may be attenuated by oligonucleotides antisense to TGF-beta 1, the results suggest a possible way for effective intervention in TGF-beta-mediated glomerulosclerosis.
引用
收藏
页码:F812 / F821
页数:10
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