首页> 外文期刊>International journal of biological sciences >Phenotypic characterization of osteoarthritic osteocytes from the sclerotic zones: A possible pathological role in subchondral bone sclerosis
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Phenotypic characterization of osteoarthritic osteocytes from the sclerotic zones: A possible pathological role in subchondral bone sclerosis

机译:硬化区骨关节炎骨细胞的表型表征:软骨下骨硬化中可能的病理作用

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摘要

Subchondral bone sclerosis is a well-recognised manifestation of osteoarthritis (OA). The osteocyte cell network is now considered to be central to the regulation of bone homeostasis; however, it is not known whether the integrity of the osteocyte cell network is altered in OA patients. The aim of this study was to investigate OA osteocyte phenotypic changes and its potential role in OA subchondral bone pathogenesis. The morphological and phenotypic changes of osteocytes in OA samples were investigated by micro-CT, SEM, histology, immunohistochemistry, TRAP staining, apoptosis assay and real-time PCR studies. We demonstrated that in OA subchondral bone, the osteocyte morphology was altered showing rough and rounded cell body with fewer and disorganized dendrites compared with the osteocytes in control samples. OA osteocyte also showed dysregulated expression of osteocyte markers, apoptosis, and degradative enzymes, indicating that the phenotypical changes in OA osteocytes were accompanied with OA subchondral bone remodelling (increased osteoblast and osteoclast activity) and increased bone volume with altered mineral content. Significant alteration of osteocytes identified in OA samples indicates a potential regulatory role of osteocytes in subchondral bone remodelling and mineral metabolism during OA pathogenesis.
机译:软骨下骨硬化是公认的骨关节炎(OA)表现。现在认为骨细胞细胞网络是调节骨稳态的关键。然而,尚不清楚OA患者骨细胞细胞网络的完整性是否改变。这项研究的目的是调查OA骨细胞表型的变化及其在骨软骨下骨发病机制中的潜在作用。通过显微CT,扫描电镜,组织学,免疫组织化学,TRAP染色,凋亡分析和实时PCR研究了OA样品中骨细胞的形态和表型变化。我们证明在OA软骨下骨中,与对照样品中的骨细胞相比,骨细胞的形态发生了变化,显示出粗糙而圆形的细胞体,树突少且杂乱无章。 OA骨细胞还显示出骨细胞标志物,细胞凋亡和降解酶的表达失调,表明OA骨细胞的表型改变伴随着OA软骨下骨重塑(增加了成骨细胞和破骨细胞的活性),并且增加了骨体积,并改变了矿物质含量。在OA样品中鉴定出的骨细胞发生重大变化,表明在OA发病机理中,骨细胞在软骨下骨重塑和矿物质代谢中具有潜在的调节作用。

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