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葡萄糖对培养的系膜细胞产生蛋白聚糖的影响。

The effect of glucose on proteoglycans produced by cultured mesangial cells.

作者信息

Silbiger S, Schlondorff D, Crowley S, Rosenberg L, Choi H, Hatcher V, Gordon P

机构信息

Department of Medicine, Montefiore Medical Center, Bronx, NY 10467.

出版信息

Diabetes. 1993 Dec;42(12):1815-22. doi: 10.2337/diab.42.12.1815.

Abstract

Altered proteoglycan metabolism may play a role in the development of diabetic glomerulopathy. This study was conducted to examine the effects of glucose on the production and physical characteristics of proteoglycans generated by rat mesangial cells in culture. Rat mesangial cells were exposed to elevated glucose media (500 mg/dl) or standard glucose media (200 mg/dl) for 8-10 days, and proteoglycan synthesis was determined using 35S-labeling in conjunction with anion exchange and sizing chromatography. Rat mesangial cells generated predominantly chondroitin/dermatan sulfate proteoglycans, with small amounts of heparan sulfate proteoglycans. High glucose did not alter the number of rat mesangial cells after 24 h or after 8-10 days, compared with cells grown under standard glucose conditions. The total amount of glycosaminoglycan generated and the sizes of the major proteoglycans were not different between cultures grown in standard and elevated glucose medium. Levels of mRNA for the proteoglycan, biglycan (as assessed by Northern blot analysis), also were comparable between the standard and elevated glucose conditions. Exposure to media high in glucose did not change the rate of secretion of proteoglycans from the cell layer to the medium, but did result in a greater quantity of radiolabeled proteoglycan deposited in the extracellular matrix. The cell, extracellular matrix and medium proteoglycans isolated from the elevated glucose cultures, consistently eluted from the anion exchange column at a lower [NaCl] compared with those generated under standard glucose conditions, indicating a loss of anionic charges.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

蛋白聚糖代谢改变可能在糖尿病肾小球病的发展中起作用。本研究旨在探讨葡萄糖对培养的大鼠系膜细胞产生的蛋白聚糖的生成及物理特性的影响。将大鼠系膜细胞置于高糖培养基(500mg/dl)或标准糖培养基(200mg/dl)中8 - 10天,采用35S标记结合阴离子交换和尺寸排阻色谱法测定蛋白聚糖的合成。大鼠系膜细胞主要产生硫酸软骨素/硫酸皮肤素蛋白聚糖,少量硫酸乙酰肝素蛋白聚糖。与在标准葡萄糖条件下生长的细胞相比,高糖在24小时后或8 - 10天后并未改变大鼠系膜细胞的数量。在标准糖培养基和高糖培养基中培养的细胞,所产生的糖胺聚糖总量及主要蛋白聚糖的大小并无差异。通过Northern印迹分析评估的蛋白聚糖双糖链蛋白聚糖的mRNA水平,在标准糖和高糖条件下也相当。暴露于高糖培养基并未改变蛋白聚糖从细胞层分泌到培养基中的速率,但确实导致更多放射性标记的蛋白聚糖沉积在细胞外基质中。与在标准葡萄糖条件下产生的蛋白聚糖相比,从高糖培养物中分离的细胞、细胞外基质和培养基中的蛋白聚糖,在较低的[NaCl]浓度下从阴离子交换柱上洗脱,表明阴离子电荷丢失。(摘要截短至250字)

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