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Osteophyte development--molecular characterization of differentiation stages.

机译:骨赘发育-分化阶段的分子特征。

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OBJECTIVE: Osteophytes are non-neoplastic osteo-cartilaginous protrusions growing at the margins of osteoarthritic joints. They can not only be considered as in situ repair tissue, but also represent an excellent in vivo model for induced cartilage repair processes. Our focus was to identify different steps of osteophyte development via analysis of expression patterns of marker genes of chondrocytic differentiation. DESIGN: We performed an extensive analysis of the presence and expression of matrix components using histochemical, immunohistochemical and in situ hybridization technology. RESULTS: Four different stages of osteophyte formation could be identified based on histomorphological and cell biological parameters: starting from mesenchymal condensates, chondrogenic differentiation is indicated by the onset of Col2A and aggrecan expression (stage I). Stage II shows fibrocartilage with an admixture of cartilaginous and fibrous matrix components such as Col2 and aggrecan on the one hand and Col1 on the other hand. The proliferating osteophyte (stage III) shows a zonal organization similar to the fetal growth plate cartilage with extensive chondrocyte hypertrophy in the zones next to ongoing endochondral bone formation. 'Mature' osteophytes (stage IV) resembled largely articular hyaline cartilage with a predominance of Col2 and aggrecan and Col6 found mainly pericellularily. CONCLUSIONS: The development of osteophytes is a good in vivo model to pursue chondrocyte differentiation from pluripotent mesenchymal cells to mature or hypertrophic chondrocytes in situ in the adult. The analysis of marker molecules of mesenchymal differentiation allows to identify different stages of repair tissue development and the transformation from fibrous tissue to neo-cartilage. Tissue architecture and matrix composition in mature osteophytes suggests that metaplastic neo-cartilagenous tissue might be one potential source of cartilage repair tissue in the adult joint.
机译:目的:骨赘是在骨关节炎关节边缘生长的非肿瘤性骨-软骨突起。它们不仅可以被认为是原位修复组织,而且代表了诱导软骨修复过程的优秀体内模型。我们的重点是通过分析软骨细胞分化标志物基因的表达模式来鉴定骨赘发育的不同步骤。设计:我们使用组织化学,免疫组织化学和原位杂交技术对基质成分的存在和表达进行了广泛的分析。结果:根据组织形态学和细胞生物学参数,可以鉴定出骨赘形成的四个不同阶段:从间充质开始,Col2A的发生和软骨聚集蛋白聚糖的表达表明软骨形成的分化(I期)。第二阶段显示纤维软骨与软骨和纤维基质成分的混合物,例如一方面是Col2和聚集蛋白聚糖,另一方面是Col1。增生的骨赘(III期)显示出与胎儿生长板软骨相似的带状组织,在软骨内骨形成附近区域中软骨细胞肥大。 “成熟的”骨赘(IV期)在很大程度上类似于关节软骨,主要是Col2和蛋白聚糖,而Col6主要在细胞周围发现。结论:成骨细胞的发育是一个良好的体内模型,可以在成人中进行软骨细胞从多能间充质细胞向成熟或肥大软骨细胞的分化。间充质分化标记分子的分析可以确定修复组织发育的不同阶段,以及从纤维组织向新软骨的转化。成熟骨赘的组织结构和基质组成表明,化生的新软骨组织可能是成年关节中软骨修复组织的一种潜在来源。

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