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Nonenzymatic glycation of mesangial matrix and prolonged exposure of mesangial matrix to elevated glucose reduces collagen synthesis and proteoglycan charge

机译:肾小球系膜基质的非酶糖基化和长时间的肾小球系膜基质暴露于升高的葡萄糖降低了胶原蛋白的合成和蛋白聚糖的电荷

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Nonenzymatic glycation of mesangial matrix and prolonged exposure of mesangial matrix to elevated glucose reduces collagen synthesis and proteoglycan charge. Expansion of the mesangial matrix in diabetes occurs after prolonged exposure to the diabetic milieu. To mimic the long-term hyperglycemia of diabetes mellitus we developed tissue culture systems that might approximate the chronic state. This was accomplished in two ways: (1) by growing mesangial cells on extracellular matrix glycated and crosslinked in vitro and (2) by continuously growing cells on their own matrix on filters in elevated glucose medium (500 mg/dl) for up to eight weeks without passage. Synthesis of collagen and proteoglycans was evaluated in cells grown under these conditions. In both these situations, 3H-proline incorporation into collagenase sensitive protein and 35S incorporation into sulfated proteins were reduced compared to control cultures. Despite reduction in 35S incorporation into proteoglycans in the high glucose cultures, total glycosaminoglycan content was unchanged. However, proteoglycans generated by mesangial cells grown in elevated glucose media were of a lower negative charge than controls. In mesangial cells continuously grown on filters, the levels of messenger RNA for collagen types I and IV, biglycan and TGF- were not different in cells grown at elevated or standard glucose concentrations for two and four weeks. We conclude that crosslinking of mesangial matrix or continuous culture of cells for prolonged periods of time in high glucose medium, which may also crosslink matrix, suppresses collagen synthesis and reduces the negative charges on matrix proteoglycans without altering mRNA levels.
机译:肾小球系膜基质的非酶糖基化和肾小球系膜基质长时间暴露于升高的葡萄糖会降低胶原蛋白的合成和蛋白聚糖的电荷。糖尿病患者肾小球系膜基质的扩展发生在长时间暴露于糖尿病环境中之后。为了模拟糖尿病的长期高血糖症,我们开发了可能近似于慢性状态的组织培养系统。这可以通过两种方式来实现:(1)通过在体外使糖基化和交联的细胞外基质上培养肾小球系膜细胞;(2)通过在葡萄糖培养基(500 mg / dl)的滤膜上使细胞在其自身基质上连续生长,最多八次。周未通过。在这些条件下生长的细胞中评估了胶原蛋白和蛋白聚糖的合成。在这两种情况下,与对照培养相比,减少了将3H-脯氨酸掺入胶原酶敏感蛋白中和将35S掺入硫酸化蛋白中。尽管在高葡萄糖培养物中减少了35S掺入蛋白聚糖的过程,但总糖胺聚糖含量没有变化。但是,由在升高的葡萄糖培养基中生长的肾小球膜细胞产生的蛋白聚糖的负电荷比对照组低。在连续在滤膜上生长的系膜细胞中,I型和IV型胶原蛋白,双糖链蛋白聚糖和TGF-β的信使RNA的水平在以升高或标准葡萄糖浓度生长2周和4周的细胞中没有差异。我们得出结论,系膜基质交联或在高葡萄糖培养基中长时间连续培养细胞,这也可能使基质交联,抑制胶原蛋白合成并减少基质蛋白聚糖上的负电荷,而不会改变mRNA水平。

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