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X型胶原蛋白在犬生长板和成年犬关节软骨中的定位。

Localization of type X collagen in canine growth plate and adult canine articular cartilage.

作者信息

Gannon J M, Walker G, Fischer M, Carpenter R, Thompson R C, Oegema T R

机构信息

Department of Orthopaedic Surgery, University of Minnesota, Minneapolis.

出版信息

J Orthop Res. 1991 Jul;9(4):485-94. doi: 10.1002/jor.1100090404.

Abstract

Type X collagen was extracted from ends of canine growth plates by pepsin digestion after 4 M guanidine hydrochloride extraction, purified by stepwise salt precipitation (2.0 M NaCl in 0.5 M acetic acid), and chromatographed on a Bio-Gel A1.5 M column in 1.0 M CaCl2. Without reduction on sodium dodecyl sulfate (SDS) polyacrylamide gels, the preparation yielded a single, high-molecular-weight (mol wt) band; after reduction, a single band of relative mol wt 5.0 x 10(4) was found. Polyclonal sera were raised against the purified collagen and used in the immunolocalization of canine type X collagen. As expected, indirect immunoperoxidase (IP) or indirect immunofluorescent staining with the polyclonal sera demonstrated that most of the immunoreactivity was localized in the zone of provisional calcification of the growth plate and in cartilage remnants in the metaphyseal region of the physis. A progressive decrease in staining toward the diaphysis of the fetal canine long bone was apparent as the trabecular structures were remodeled to bone. Unexpectedly, type X collagen was also detected in the zone of calcified, mature articular cartilage. It was concentrated in the pericellular matrix of the chondrocytes, appeared at or just above the tidemark, and was expressed immediately before mineralization. Identification of type X collagen in both the canine growth plate and the zone of calcified articular cartilage suggests that cells in the deep layer of cartilage and in the zone of calcified cartilage in the adult animal retain some characteristics of a growth plate and may be involved in regulation of mineralization at this critical interface. The expression of growth plate-like properties would allow the deep chondrocytes of mature articular cartilage to play a role in remodeling of the joint with age and in the pathogenesis of osteoarthritis.

摘要

在4M盐酸胍提取后,通过胃蛋白酶消化从犬生长板末端提取X型胶原蛋白,经逐步盐沉淀(在0.5M乙酸中加入2.0M氯化钠)纯化,并在1.0M氯化钙中于Bio-Gel A1.5M柱上进行层析。在十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶上不进行还原时,该制剂产生一条单一的高分子量(分子量)条带;还原后,发现一条相对分子量为5.0×10⁴的单一条带。制备了针对纯化胶原蛋白的多克隆血清,并用于犬X型胶原蛋白的免疫定位。正如预期的那样,用多克隆血清进行间接免疫过氧化物酶(IP)或间接免疫荧光染色表明,大部分免疫反应性定位于生长板的临时钙化区和干骺端区域的软骨残余物中。随着小梁结构重塑为骨,向胎儿犬长骨干骺端的染色逐渐减少是明显的。出乎意料的是,在钙化的成熟关节软骨区域也检测到了X型胶原蛋白。它集中在软骨细胞的细胞周基质中,出现在潮线处或潮线稍上方,并在矿化前立即表达。在犬生长板和钙化关节软骨区域中均鉴定出X型胶原蛋白,这表明成年动物软骨深层和钙化软骨区域的细胞保留了生长板的一些特征,并且可能参与了这个关键界面处的矿化调节。生长板样特性的表达将使成熟关节软骨的深层软骨细胞在关节随年龄的重塑以及骨关节炎的发病机制中发挥作用。

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