Kolm V, Sauer U, Olgemöller B, Schleicher E D
Institute for Diabetes Research, Department of Biochemistry, Academic Hospital, University of Munich, Germany.
Am J Physiol. 1996 May;270(5 Pt 2):F812-21. doi: 10.1152/ajprenal.1996.270.5.F812.
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.
以往的研究表明,在高糖浓度下培养系膜细胞会刺激细胞外基质合成,还会增加转化生长因子-β(TGF-β)的表达。我们研究了高血糖对系膜细胞增殖以及硫酸乙酰肝素蛋白聚糖(HSPG)和纤连蛋白产生的影响。系膜细胞长时间暴露于不断升高的葡萄糖浓度下,会对生长抑制和基质产生刺激产生剂量依赖性效应。用高糖条件培养基或TGF-β1处理系膜细胞可模拟高糖孵育的效应。此外,TGF-β1导致HSPG mRNA水平呈剂量依赖性增加。高糖对系膜细胞的作用之前,总TGF-β1蛋白会增加。TGF-β1反义寡核苷酸的存在减弱了葡萄糖对系膜细胞增殖和基质产生的介导作用。数据表明,即使是适度升高的葡萄糖浓度似乎也会影响系膜细胞。结果表明:1)TGF-β1蛋白的产生是获得高糖诱导效应所必需的;2)TGF-β1刺激系膜细胞HSPG的表达和产生。由于这些效应可能会被TGF-β1反义寡核苷酸减弱,因此结果提示了一种有效干预TGF-β介导的肾小球硬化的可能途径。