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生长猪关节-骺软骨中蛋白聚糖的体外产生

In vitro production of proteoglycans in the articular-epiphyseal cartilage of growing pigs.

作者信息

Ekman S, Unger E, Kjellén L

机构信息

Department of Anatomy & Histology, Swedish University of Agricultural Sciences, Uppsala.

出版信息

Glycoconj J. 1994 Apr;11(2):81-8. doi: 10.1007/BF00731147.

Abstract

The failure of cartilage mineralization in osteochondrotic cartilage may be due to an impaired proteoglycan production. The in vitro production of proteoglycans was therefore studied in the joint cartilage of growing pigs, aged 9-18 weeks, after incubation of cartilage samples with 35S-sulfate. Cartilage was obtained from different areas of the femoral condyles and samples from these areas were further divided into three layers, where the superficial layer contains articular cartilage and the basal layers consist of growth cartilage. There was no significant difference in the overall amount of 35S-proteoglycans synthesized in different areas of the condyles. However, the total production of 35S-proteoglycans per mg tissue was highest in the basal layer in all areas. This was not due to a larger number of cells; the superficial layer contained more DNA per mg tissue than the basal layer. Gel chromatography on Sepharose CL-2B of the cartilage extracts, which resulted in the separation of large proteoglycans (Kav approximately 0.4) from proteoglycans of small hydrodynamic size (Kav approximately 0.8), showed that the relative amount of large proteoglycans increased with the distance from the articular surface. Again, no difference in the relative amounts of large and small proteoglycans were found when cartilage from different areas were compared. Osteochondrotic cartilage was detected in the pigs aged 12-18 weeks. In areas where osteochondrotic cartilage were present, the total production of 35S-proteoglycans was lowered and the relative amount of large proteoglycans was less than that found in the adjoining areas devoid of osteochondrotic lesions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

骨软骨病性软骨中软骨矿化失败可能是由于蛋白聚糖产生受损。因此,在用35S - 硫酸盐孵育软骨样本后,对9至18周龄生长猪的关节软骨中蛋白聚糖的体外产生进行了研究。软骨取自股骨髁的不同区域,这些区域的样本进一步分为三层,其中表层包含关节软骨,基层由生长软骨组成。在髁的不同区域合成的35S - 蛋白聚糖总量没有显著差异。然而,所有区域中每毫克组织的35S - 蛋白聚糖总产量在基层最高。这并非由于细胞数量更多;表层每毫克组织所含的DNA比基层更多。对软骨提取物在Sepharose CL - 2B上进行凝胶色谱分析,可将大型蛋白聚糖(洗脱体积约0.4)与流体动力学尺寸小的蛋白聚糖(洗脱体积约0.8)分离,结果表明大型蛋白聚糖的相对量随着距关节表面距离的增加而增加。同样,比较不同区域的软骨时,未发现大型和小型蛋白聚糖的相对量有差异。在12至18周龄的猪中检测到骨软骨病性软骨。在存在骨软骨病性软骨的区域,35S - 蛋白聚糖的总产量降低,大型蛋白聚糖的相对量低于相邻无骨软骨病性病变区域。(摘要截断于250字)

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