McQuillan D J, Handley C J, Robinson H C
Biochem J. 1986 Aug 1;237(3):741-7. doi: 10.1042/bj2370741.
Proteoglycan synthesis in explant cultures of adult bovine articular cartilage is stimulated in a dose-dependent manner when the tissue is cultured in the presence of foetal-calf serum. The stimulation of proteoglycan synthesis is paralleled by a similar increase in DNA synthesis; however, when DNA synthesis is inhibited by hydroxyurea the stimulation of proteoglycan synthesis by serum remains essentially the same. The apparent half-life of the pool of proteoglycan core protein precursor was measured in freshly isolated tissue as well as in tissue cultured for 7 days in the presence and in the absence of foetal-calf serum; under all conditions the half-life was the same, suggesting that this value is independent of the net rate of proteoglycan synthesis. In the presence of actinomycin D, an inhibitor of RNA synthesis, there was a difference in the apparent half-life of the available pool of mRNA coding for proteoglycan core protein: 8.5 h for tissue maintained in the presence of serum and 3.8 h for tissue cultured in the absence of serum. It is suggested that proteoglycan synthesis is stimulated by serum factors at the level of DNA-dependent RNA synthesis. Concomitant with an increase in the rate of proteoglycan synthesis induced by the presence of serum in the culture medium, an increase in the concentrations of several glycosyltransferases involved in chondroitin sulphate synthesis was also observed.
当成年牛关节软骨外植体培养物在胎牛血清存在的情况下进行培养时,蛋白聚糖的合成以剂量依赖的方式受到刺激。蛋白聚糖合成的刺激与DNA合成的类似增加同时出现;然而,当DNA合成被羟基脲抑制时,血清对蛋白聚糖合成的刺激基本保持不变。在新鲜分离的组织以及在有和没有胎牛血清的情况下培养7天的组织中,测量了蛋白聚糖核心蛋白前体池的表观半衰期;在所有条件下,半衰期都是相同的,这表明该值与蛋白聚糖合成的净速率无关。在RNA合成抑制剂放线菌素D存在的情况下,编码蛋白聚糖核心蛋白的可用mRNA池的表观半衰期存在差异:在血清存在下维持的组织为8.5小时,在无血清条件下培养的组织为3.8小时。有人提出,血清因子在依赖DNA的RNA合成水平上刺激蛋白聚糖的合成。与培养基中血清的存在所诱导的蛋白聚糖合成速率增加同时,还观察到参与硫酸软骨素合成的几种糖基转移酶的浓度增加。