Hunter G K, Weinert C A
Faculty of Dentistry, University of Western Ontario, London, Canada.
Connect Tissue Res. 1996;35(1-4):379-84. doi: 10.3109/03008209609029215.
In order to determine the role of proteoglycan in the calcification of cartilage, the effects on calcifying chondrocyte cultures of treatments that disrupt proteoglycan biosynthesis have been studied. Treatment of secondary cultures of embryonic chick chondrocytes with non-toxic concentrations of the beta-xyloside p-nitrophenyl beta-D-xylopyranoside (PNPX) resulted in dose-dependent inhibition of both proteoglycan and mineral deposition. Based on the expression of Type X collagen, however, PNPX is also a potent inhibitor of chondrocyte differentiation. Under-sulfation of proteoglycans was effected by growth of chondrocyte cultures in sulfate-depleted medium. Growth in low-sulfate medium did not significantly affect the growth or differentiation of these cultures, but caused an approximate two-fold decrease in mineral content compared to cultures grown in normal medium. These findings indicate that disruption of proteoglycan biosynthesis in chondrocyte cultures results in decreased levels of calcification. Therefore, proteoglycans appear to function as promoters of chondrocyte calcification.
为了确定蛋白聚糖在软骨钙化中的作用,研究了破坏蛋白聚糖生物合成的处理对钙化软骨细胞培养物的影响。用无毒浓度的β-木糖苷对硝基苯基β-D-吡喃木糖苷(PNPX)处理胚胎鸡软骨细胞的传代培养物,导致蛋白聚糖和矿物质沉积均呈剂量依赖性抑制。然而,基于X型胶原的表达,PNPX也是软骨细胞分化的有效抑制剂。蛋白聚糖的硫酸化不足是通过在硫酸盐缺乏的培养基中培养软骨细胞来实现的。在低硫酸盐培养基中生长对这些培养物的生长或分化没有显著影响,但与在正常培养基中生长的培养物相比,矿物质含量降低了约两倍。这些发现表明,软骨细胞培养物中蛋白聚糖生物合成的破坏导致钙化水平降低。因此,蛋白聚糖似乎起着软骨细胞钙化促进剂的作用。