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大鼠肋软骨中硫酸软骨素蛋白聚糖的降解模式

Mode of degradation of the chondroitin sulphate proteoglycan in rat costal cartilage.

作者信息

Wasteson A, Lindahl U, Hallén A

出版信息

Biochem J. 1972 Dec;130(3):729-38. doi: 10.1042/bj1300729.

Abstract
  1. Chondroitin sulphate was isolated from different regions of rat costal cartilage after extensive proteolysis of the tissues. The molecular weight, determined by gel chromatography, of the polysaccharide obtained from an actively growing region (lateral zone) near the osteochondral junction was higher than that of the polysaccharide isolated from the remaining portion of the costal cartilage (medial zone). 2. In both types of cartilage the molecular weight of chondroitin sulphate, labelled with [(35)S]sulphate, remained unchanged in vivo over a period of 10 days, approximately corresponding to the half-life of the chondroitin sulphate proteoglycan. The molecular-weight distribution of chondroitin [(35)S]sulphate, labelled in vivo or in vitro, was invariably identical with that of the bulk polysaccharide from the same tissue. It is concluded that the observed regional variations in molecular-weight distribution were established at the time of polysaccharide biosynthesis. 3. In tissue culture more than half of the (35)S-labelled polysaccharide-proteins of the two tissues was released into the medium within 10 days of incubation. The released materials were of smaller molecular size than were the corresponding native proteoglycans. In contrast, the molecular-weight distribution of the chondroitin [(35)S]sulphate (single polysaccharide chains) remained constant throughout the incubation period. 4. A portion (about 20%) of the total radioactive material released from (35)S-labelled cartilage in tissue culture was identified as inorganic [(35)S]sulphate. No corresponding decrease in the degree of sulphation of the labelled polysaccharide could be detected. These findings suggest that a limited fraction of the proteoglycan molecules had been extensively desulphated. 5. It is suggested that the initial phase of degradation involves proteolytic cleavage of the proteoglycan, but the constituent polysaccharide chains remain intact. The partially degraded proteoglycan may be eliminated from the cartilage by diffusion into the circulatory system. An additional degradative process, which may occur intracellularly, includes desulphation of the polysaccharide, probably in conjunction with a more extensive breakdown of the polymer.
摘要
  1. 在对大鼠肋软骨组织进行广泛的蛋白水解后,从其不同区域分离出硫酸软骨素。通过凝胶色谱法测定,从骨软骨交界处附近活跃生长区域(外侧区)获得的多糖的分子量高于从肋软骨其余部分(内侧区)分离出的多糖的分子量。2. 在这两种类型的软骨中,用[³⁵S]硫酸盐标记的硫酸软骨素的分子量在体内10天内保持不变,大约相当于硫酸软骨素蛋白聚糖的半衰期。体内或体外标记的硫酸软骨素[³⁵S]的分子量分布始终与来自同一组织的大量多糖的分子量分布相同。由此得出结论,观察到的分子量分布的区域差异是在多糖生物合成时确定的。3. 在组织培养中,两种组织中超过一半的³⁵S标记的多糖蛋白在培养10天内释放到培养基中。释放的物质的分子大小比相应的天然蛋白聚糖小。相比之下,硫酸软骨素[³⁵S](单多糖链)的分子量分布在整个培养期间保持不变。4. 组织培养中从³⁵S标记的软骨释放的总放射性物质的一部分(约20%)被鉴定为无机[³⁵S]硫酸盐。未检测到标记多糖的硫酸化程度有相应降低。这些发现表明,有限比例的蛋白聚糖分子已被广泛脱硫。5. 有人提出,降解的初始阶段涉及蛋白聚糖的蛋白水解裂解,但组成多糖链保持完整。部分降解的蛋白聚糖可能通过扩散进入循环系统而从软骨中清除。另一个可能发生在细胞内的降解过程包括多糖的脱硫,可能与聚合物的更广泛分解同时发生。

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