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短肢畸形(bm/bm)小鼠软骨中的蛋白聚糖和糖胺聚糖

Proteoglycans and glycosaminoglycans in cartilage from the brachymorphic (bm/bm) mouse.

作者信息

Wikström B, Engfeldt B, Heinegård D, Hjerpe A

出版信息

Coll Relat Res. 1985 Mar;5(2):193-204. doi: 10.1016/s0174-173x(85)80040-6.

Abstract

The brachymorphic (bm/bm) mouse is a disproportionate dwarf with a disturbance of the endochondral growth of the skeleton. Rib cartilage from 25-day-old affected animals and their normal siblings was analyzed for its contents and composition of proteoglycans. In addition to the previously reported undersulfation of chondroitin sulfate, it was demonstrated that one of the two types of aggregating proteoglycan and possibly the small ones are decreased in bm/bm costal cartilage, both in the growth region and in the remaining part. The molecular defect of the bm/bm condition is known to affect the synthesis of 3-phosphoadenosine 5-phosphosulfate (Sugahara and Schwartz, Proc. Natl. Acad. Sci. USA 76: 6615-6618, 1979). The above finding therefore suggests the existence of feedback mechanisms for the regulation of proteoglycan synthesis, whereby the undersulfation of glycosaminoglycans would result in decreased synthesis or increased turnover of certain proteoglycan subpopulations. Analysis of the glycosaminoglycan side chains indicated that mouse rib cartilage contains small amounts of keratan sulfate of extremely small size. The affected and control tissues, however, seemed to contain equal amounts of both glucosamine and galactosamine.

摘要

短形(bm/bm)小鼠是一种不成比例的侏儒,其软骨内骨骼生长受到干扰。对25日龄患病动物及其正常同胞的肋软骨进行了蛋白聚糖含量和组成分析。除了先前报道的硫酸软骨素硫酸化不足外,还证明在bm/bm肋软骨中,无论是生长区域还是其余部分,两种聚集型蛋白聚糖中的一种以及可能的小分子蛋白聚糖都减少了。已知bm/bm状态的分子缺陷会影响3-磷酸腺苷5-磷酸硫酸酯的合成(Sugahara和Schwartz,《美国国家科学院院刊》76:6615 - 6618,1979)。因此,上述发现表明存在调节蛋白聚糖合成的反馈机制,据此糖胺聚糖硫酸化不足会导致某些蛋白聚糖亚群的合成减少或周转增加。对糖胺聚糖侧链的分析表明,小鼠肋软骨含有少量极小尺寸的硫酸角质素。然而,患病组织和对照组织似乎含有等量的氨基葡萄糖和半乳糖胺。

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