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Role of caveolae in high glucose and TGF-?21 induced fibronectin production in rat mesangial cells

机译:小窝蛋白在高糖和TGF-β21诱导的大鼠肾小球系膜细胞中产生纤连蛋白的作用

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Accumulation of extracellular matrix (ECM) in glomerular mesangium correlates with loss of renal function in diabetic nephropathy. However, the mechanisms underlying are still incompletely known. In the present study, we explored the role of caveolae in ECM production in rat mesangial cells (MCs) stimulated by high glucose or transforming growth factor-β1 (TGF-β1), and investigated the possible mechanisms. High glucose (HG) or TGF-β1 significantly increased collagen-1 and fibronectin expression at both mRNA and protein levels in time- course dependent manners, and simultaneously induced caveolin-1 tyrosine phosphorylation. Disruption of caveolae with Methyl-β-cyclodextrin (β-MCD) prevented HG and TGF-β1 induced caveolin-1 tyrosine phosphorylation, and attenuated fibronectin but not collagen-1 production. This effect of β-MCD on fibronectin production could be abolished by cholesterol, which restored HG and TGF-β1 induced caveolin-1 tyrosine phosphorylation. In addition, HG and TGF-β1 induced fibronectin production was attenuated by a caveolin-1 scaffold domain peptide. These findings indicate that mesangial cell caveolae regulate fibronectin production at least partly through caveolin-1 phosphorylation.
机译:肾小球系膜中细胞外基质(ECM)的积累与糖尿病肾病中肾功能的丧失有关。但是,底层机制仍不完全清楚。在本研究中,我们探讨了小窝在高糖或转化生长因子-β1(TGF-β1)刺激的大鼠系膜细胞(MC)中ECM产生中的作用,并研究了可能的机制。高葡萄糖(HG)或TGF-β1以时程依赖性方式在mRNA和蛋白水平上均显着增加了胶原蛋白1和纤连蛋白的表达,同时诱导了小窝蛋白1酪氨酸的磷酸化。用甲基-β-环糊精(β-MCD)破坏小窝可阻止HG和TGF-β1诱导小窝1酪氨酸磷酸化,并减弱纤连蛋白,但不能减少1型胶原的产生。 β-MCD对纤连蛋白产生的这种影响可以被胆固醇消除,胆固醇可以恢复HG和TGF-β1诱导的小窝蛋白1酪氨酸磷酸化。此外,caveolin-1支架结构域肽减弱了HG和TGF-β1诱导的纤连蛋白的产生。这些发现表明肾小球系膜细胞caveolae至少部分通过caveolin-1磷酸化调节纤连蛋白的产生。

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