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骨赘形成——分化阶段的分子特征

Osteophyte development--molecular characterization of differentiation stages.

作者信息

Gelse K, Söder S, Eger W, Diemtar T, Aigner T

机构信息

Cartilage Research, Department of Pathology, University of Erlangen-Nürnberg, Federal Republic of Germany.

出版信息

Osteoarthritis Cartilage. 2003 Feb;11(2):141-8. doi: 10.1053/joca.2002.0873.

Abstract

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.

摘要

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出物。它们不仅可被视为原位修复组织,而且代表了诱导软骨修复过程的优良体内模型。我们的重点是通过分析软骨细胞分化标记基因的表达模式来确定骨赘发育的不同阶段。

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分析。

结果

根据组织形态学和细胞生物学参数可确定骨赘形成的四个不同阶段:从间充质凝聚开始,Ⅱ型胶原(Col2A)和聚集蛋白聚糖表达的开始表明软骨形成分化(Ⅰ期)。Ⅱ期显示纤维软骨,一方面混合有软骨和纤维基质成分,如Ⅱ型胶原和聚集蛋白聚糖,另一方面有Ⅰ型胶原。增殖性骨赘(Ⅲ期)表现出与胎儿生长板软骨相似的带状组织,在正在进行的软骨内骨形成旁边的区域有广泛的软骨细胞肥大。“成熟”骨赘(Ⅳ期)在很大程度上类似于关节透明软骨,以Ⅱ型胶原和聚集蛋白聚糖为主,Ⅵ型胶原主要在细胞周围发现。

结论

骨赘的发育是研究成年期多能间充质细胞原位分化为成熟或肥大软骨细胞的良好体内模型。对间充质分化标记分子的分析有助于识别修复组织发育的不同阶段以及从纤维组织到新软骨的转变。成熟骨赘的组织结构和基质组成表明,化生新软骨组织可能是成年关节软骨修复组织的一个潜在来源。

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