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通过聚集蛋白聚糖的生物素化结合区域探测透明质酸在关节软骨中的分布。

Distribution of hyaluronan in articular cartilage as probed by a biotinylated binding region of aggrecan.

作者信息

Parkkinen J J, Häkkinen T P, Savolainen S, Wang C, Tammi R, Agren U M, Lammi M J, Arokoski J, Helminen H J, Tammi M I

机构信息

Department of Anatomy, University of Kuopio, Finland.

出版信息

Histochem Cell Biol. 1996 Mar;105(3):187-94. doi: 10.1007/BF01462291.

Abstract

The proportion of total tissue hyaluronan involved in interactions with aggrecan and link protein was estimated from extracts of canine knee articular cartilages using a biotinylated hyaluronan binding region-link protein complex (bHABC) of proteoglycan aggregate as a probe in an ELISA-like assay. Microscopic sections were stained with bHABC to reveal free hyaluronan in various sites and zones of the cartilages. Articular cartilage, cut into 20 microns-thick sections, was extracted with 4 M guanidinium chloride (GuCl). Aliquots of the extract (after removing GuCl) were assayed for hyaluronan, before and after papain digestion. The GuCl extraction residues were analyzed after solubilization by papain. It was found that 47-51% of total hyaluronan remained in the GuCl extraction residue, in contrast to the 8-15% of total proteoglycans. Analysis of the extract revealed that 24-50% of its hyaluronan was directly detectable with the probe, while 50-76% became available only after protease digestion. The extracellular matrix in cartilage sections was stained with the bHABC probe only in the superficial zone and the periphery of the articular surfaces, both sites known to have a relatively low proteoglycan concentration. Trypsin pretreatment of the sections enhanced the staining of the intermediate and deep zones, presumably by removing the steric obstruction caused by the chondroitin sulfate binding region of aggrecans. Enhanced matrix staining in these zones was also obtained by a limited digestion with chondroitinase ABC. The results indicate that a part of cartilage hyaluronan is free from endogenous binding proteins, such as aggrecan and link protein, but that the chondroitin sulfate-rich region of aggrecan inhibits its probing in intact tissue sections. Therefore, hyaluronan staining was more intense in cartilage areas with lower aggrecan content. A large proportion of hyaluronan resists GuCl extraction, even from 20-micrograms-thick tissue sections.

摘要

使用蛋白聚糖聚集体的生物素化透明质酸结合区域-连接蛋白复合物(bHABC)作为探针,通过类似酶联免疫吸附测定(ELISA)的方法,从犬膝关节软骨提取物中估算参与与聚集蛋白聚糖和连接蛋白相互作用的总组织透明质酸的比例。用bHABC对显微切片进行染色,以揭示软骨不同部位和区域中的游离透明质酸。将关节软骨切成20微米厚的切片,用4M氯化胍(GuCl)进行提取。提取物的等分试样(去除GuCl后)在木瓜蛋白酶消化前后进行透明质酸检测。木瓜蛋白酶溶解后对GuCl提取残留物进行分析。结果发现,总透明质酸的47%-51%保留在GuCl提取残留物中,而总蛋白聚糖的这一比例为8%-15%。对提取物的分析表明,其24%-50%的透明质酸可用探针直接检测到,而50%-76%仅在蛋白酶消化后才可用。软骨切片中的细胞外基质仅在浅表区和关节表面周边用bHABC探针染色,这两个部位的蛋白聚糖浓度相对较低。切片经胰蛋白酶预处理后,中间区和深层区的染色增强,推测是通过去除聚集蛋白聚糖硫酸软骨素结合区域造成的空间阻碍。通过用硫酸软骨素酶ABC进行有限消化,也可在这些区域获得增强的基质染色。结果表明,软骨透明质酸的一部分没有内源性结合蛋白(如聚集蛋白聚糖和连接蛋白),但聚集蛋白聚糖富含硫酸软骨素的区域会抑制其在完整组织切片中的检测。因此,在聚集蛋白聚糖含量较低的软骨区域,透明质酸染色更强烈。即使是从20微米厚的组织切片中,很大一部分透明质酸也能抵抗GuCl提取。

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