首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Role of proteoglycans in endochondral ossification: immunofluorescent localization of link protein and proteoglycan monomer in bovine fetal epiphyseal growth plate
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Role of proteoglycans in endochondral ossification: immunofluorescent localization of link protein and proteoglycan monomer in bovine fetal epiphyseal growth plate

机译:蛋白聚糖在软骨内骨化中的作用:牛胎儿骨phy生长板中连接蛋白和蛋白聚糖单体的免疫荧光定位

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摘要

The hypothesis is widely held that, in growth plate during endochondral ossification, proteoglycans in the extracellular matrix of the lower hypertrophic zone are degraded by proteases and removed before mineralization, and that this is the mechanism by which a noncalcifiable matrix is transformed into a calcifiable matrix. We have evaluated this hypothesis by examining the immunofluorescent localization and concentrations of proteoglycan monomer core protein and link protein, and the concentrations of glycosaminoglycans demonstrated by safranin 0 staining, in the different zones of the bovine fetal cartilage growth plate. Monospecific antibodies were prepared to proteoglycan monomer core protein and to link protein. The immunofluorescent localization of these species was examined in decalcified and undecalcified sections containing the zones of proliferating and hypertrophic chondrocytes and in sections containing the zones of proliferating and hypertrophic chondrocytes and the metaphysis, decalcified in 0.5 M EDTA, pH 7.5, in the presence of protease inhibitors. Proteoglycan monomer core protein and link protein are demonstrable without detectable loss throughout the extracellular matrix of the longitudinal septa of the hypertrophic zone and in the calcified cartilage of the metaphysis. In fact, increased staining is observed in the calcifying cartilage. Contrary to the prevailing hypothesis, our results indicate that there is no net loss of proteoglycans during mineralization and that the proteoglycans become entombed in the calcified cartilage which provides a scaffolding on which osteoid and bone are formed. Proteoglycans appear to persist unaltered in the calcified cartilage core of the trabeculae, until at last the entire trabeculae are eroded from their surfaces and removed by osteoclasts, when the primary spongiosa is replaced by the secondary spongiosa.
机译:该假设被广泛认为,在软骨内骨化期间的生长板中,下肥大区的细胞外基质中的蛋白聚糖被蛋白酶降解并在矿化之前被去除,这是不可钙化基质转化为可钙化基质的机制。 。我们通过检查牛胎儿软骨生长板不同区域中蛋白聚糖单体核心蛋白和连接蛋白的免疫荧光定位和浓度以及番红素0染色证明的糖胺聚糖浓度,评估了这一假设。制备了蛋白聚糖单体核心蛋白和连接蛋白的单特异性抗体。在存在蛋白酶的情况下,在0.5 M EDTA,pH 7.5下,在含有增生和肥大的软骨细胞区域的脱钙和未脱钙的切片以及含有增生和肥大的软骨细胞和干sections端的区域的切片中检查了这些物种的免疫荧光定位。抑制剂。蛋白聚糖单体核心蛋白和连接蛋白是可证实的,在肥大区纵向隔垫的整个细胞外基质中以及在干physi端的钙化软骨中均未检测到损失。实际上,在钙化软骨中观察到染色增加。与普遍的假设相反,我们的结果表明在矿化过程中蛋白聚糖没有净损失,蛋白聚糖被包埋在钙化的软骨中,钙化的软骨提供了形成类骨和骨骼的支架。蛋白聚糖似乎在小梁的钙化软骨核心中保持不变,直到最终将整个小梁从其表面侵蚀并被破骨细胞清除,此时原发性海绵状海绵状细胞被继发性海绵状海绵状细胞所取代。

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