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抗坏血酸对软骨细胞培养中芳基硫酸酯酶活性和硫酸化蛋白聚糖代谢的影响。

Effect of ascorbic acid on arylsulfatase activities and sulfated proteoglycan metabolism in chondrocyte cultures.

作者信息

Schwartz E R, Adamy L

出版信息

J Clin Invest. 1977 Jul;60(1):96-106. doi: 10.1172/JCI108774.

Abstract

A correlation between increased arylsulfatase activities and decreased sulfated proteoglycan content in human osteoarthritic articular cartilage suggested a possible interrelationship between these parameters. Since we had previously shown that ascorbate caused a decrease in levels of arylsulfatase A and B activities in normal chondrocyte cultures, the validity of the above relationship was examined by measuring the effect of vitamin C on the biosynthesis and distribution of 35S-labeled proteoglycans and arylsulfatase A and B activities in cell extracts of chondrocytes derived from normal and osteoarthritic tissue. Arylsulfatase A and B activities were found to be reduced in the presence of ascorbic acid in all normal and osteoarthritic cell lines examined when measured 3, 6, 10, and 13 days after the introduction of the vitamin in the culture medium. Acid phosphatase activity, on the other hand, was found to be elevated in the presence of ascorbate. The inhibitory effect by ascorbic acid on arylsulfatase activities could be reversed by withdrawing the vitamin from the nutrient medium. Addition of EDTA to the cell extracts before assay also reversed the inhibiton. Sulfated proteoglycan biosynthesis as reflected in 35S-sulfate uptake per milligram of DNA was significantly increased in the presence of ascorbic acid. The distribution of the newly synthesized molecules between the cell layer and medium fractions was altered. In the presence of ascorbate, more deposition into the cell layer of newly synthesized macromolecules occurred. These data suggest an inverse relationship between arylsulfatase activities and the stability of the newly synthesized sulfated proteoglycans in the extracellular matrix.

摘要

人类骨关节炎关节软骨中芳基硫酸酯酶活性增加与硫酸化蛋白聚糖含量降低之间的相关性表明,这些参数之间可能存在相互关系。由于我们之前已表明抗坏血酸会导致正常软骨细胞培养物中芳基硫酸酯酶A和B的活性水平降低,因此通过测量维生素C对来自正常和骨关节炎组织的软骨细胞提取物中35S标记的蛋白聚糖的生物合成和分布以及芳基硫酸酯酶A和B活性的影响,来检验上述关系的有效性。当在培养基中加入维生素后3、6、10和13天进行测量时,发现在所有检测的正常和骨关节炎细胞系中,抗坏血酸存在时芳基硫酸酯酶A和B的活性均降低。另一方面,发现抗坏血酸存在时酸性磷酸酶活性升高。通过从营养培养基中去除维生素,可以逆转抗坏血酸对芳基硫酸酯酶活性的抑制作用。在测定前向细胞提取物中加入乙二胺四乙酸(EDTA)也可逆转这种抑制作用。抗坏血酸存在时,每毫克DNA的35S-硫酸盐摄取量所反映的硫酸化蛋白聚糖生物合成显著增加。新合成分子在细胞层和培养基部分之间的分布发生了改变。在抗坏血酸存在的情况下,新合成的大分子更多地沉积到细胞层中。这些数据表明芳基硫酸酯酶活性与细胞外基质中新合成硫酸化蛋白聚糖的稳定性之间存在负相关关系。

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