Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, OX 7LD, UK.
Virchows Arch. 2012 Aug;461(2):205-10. doi: 10.1007/s00428-012-1274-3. Epub 2012 Jul 11.
Multinucleated cells termed chondroclasts have been observed on the deep surface of resorbed hyaline cartilage but the relationship of these cells to macrophages and osteoclasts and their role in rheumatoid arthritis (RA) and other arthritic conditions is uncertain. Multinucleated cells in RA and other arthritic conditions showing evidence of cartilage resorption were characterised immunohistochemically for expression of macrophage/osteoclast markers. Mature human osteoclasts formed from circulating monocytes and tissue macrophages were cultured for up to 4 days on slices of human cartilage and glycosaminoglycan (GAG) release was measured. Multinucleated cells resorbing unmineralised cartilage were seen in osteoarthritis, RA, septic arthritis, avascular necrosis and in four cases of giant cell tumour of bone that had extended through the subchondral bone plate. Chondroclasts expressed an osteoclast-like phenotype (TRAP+, cathepsin K+, MMP9+, CD14-, HLA-DR-, CD45+, CD51+ and CD68+). Both macrophages and osteoclasts cultured on cartilage released GAG. These findings indicate that chondroclasts have an osteoclast-like phenotype and that mature human osteoclasts are capable of cartilage matrix resorption. Resorption of unmineralised subchondral cartilage by chondroclasts and macrophages can be a feature of joint destruction in inflammatory and non-inflammatory arthropathies as well as inflammatory and neoplastic subchondral bone lesions.
已在被吸收的透明软骨的深部表面观察到多核细胞,称为破骨细胞,但其与巨噬细胞和破骨细胞的关系及其在类风湿关节炎(RA)和其他关节炎中的作用尚不确定。RA 和其他关节炎中显示出软骨吸收证据的多核细胞通过免疫组织化学方法对巨噬细胞/破骨细胞标志物的表达进行了特征描述。从循环单核细胞和成体组织巨噬细胞中培养成熟的人类破骨细胞,在人软骨切片上培养长达 4 天,并测量糖胺聚糖(GAG)的释放。在骨关节炎、RA、化脓性关节炎、缺血性坏死和四例骨巨细胞瘤中观察到正在吸收未矿化软骨的破骨细胞,这些肿瘤已经穿过软骨下骨板。破骨细胞表达破骨细胞样表型(TRAP+、组织蛋白酶 K+、MMP9+、CD14-、HLA-DR-、CD45+、CD51+和 CD68+)。在软骨上培养的巨噬细胞和破骨细胞均释放 GAG。这些发现表明破骨细胞具有破骨细胞样表型,并且成熟的人类破骨细胞能够吸收软骨基质。软骨下未矿化软骨被破骨细胞和巨噬细胞吸收可能是炎症性和非炎症性关节病以及炎症性和肿瘤性软骨下骨病变中关节破坏的特征。