Department of Orthopaedics and Traumatology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong.
Osteoarthritis Cartilage. 2013 Apr;21(4):574-81. doi: 10.1016/j.joca.2013.01.002. Epub 2013 Jan 9.
This study aimed to investigate the spatial and temporal subchondral bone change of Dunkin-Hartley (DH) strain guinea pigs spontaneous osteoarthritis (OA) model at early stage with three-dimensional Microfocal Computed Tomography (Micro-CT) analysis, histology and immunohistochemistry.
Knee joints of DH and Bristol Strain 2 (BS2) guinea pigs were analyzed at 1, 2 and 3 months of age for early staged subchondral bone ultrastructure change of OA by Micro-CT and histology. And cartilage degeneration was monitored by histological examination. In addition, expression of Osterix was quantified by immunohistochemistry.
Microscopic cartilage degeneration was not found at first 3 months in both DH and BS2 guinea pigs. Subchondral bone sclerosis with trabecular ultrastructure turnover was characterized in subchondral bone of DH guinea pigs. Increased thickness, bone mineral density with decreased porosity were defined in subchondral plate of DH guinea pigs. Subchondral trabecular bone was found to be plate-like, convex and isotropy with higher bone volume. Histology confirmed the finding of lower porosity at osteochondral junction and increased bone volume. Immunohistochemistry revealed that the early OA subchondral bone change may be due to elevated level of osteoblast differentiation.
Subchondral bone ultrastructure change occurred at early stage of OA ahead of microscopic cartilage degeneration, which may further impair articular cartilage. It was possibly related to elevated level of osteoblast differentiation.
本研究旨在通过三维微焦点计算机断层扫描(Micro-CT)分析、组织学和免疫组织化学方法,研究 Dunkin-Hartley(DH)品系豚鼠自发性骨关节炎(OA)模型早期关节软骨下骨的时空变化。
分析 DH 和 Bristol Strain 2(BS2)豚鼠膝关节在 1、2 和 3 月龄时的早期 OA 软骨下骨超微结构变化。通过组织学检查监测软骨退变。并用免疫组织化学法定量检测成骨细胞标志物 Osterix 的表达。
在最初的 3 个月内,DH 和 BS2 豚鼠的软骨均未出现显微镜下的退变。DH 豚鼠的软骨下骨表现为骨硬化,伴有小梁超微结构的更替。DH 豚鼠的软骨下板表现为厚度增加、骨密度增加、孔隙率降低。软骨下骨小梁呈板状、凸状、各向同性,骨量增加。组织学证实骨软骨交界处的孔隙率较低,骨量增加。免疫组织化学显示,早期 OA 软骨下骨变化可能与成骨细胞分化水平升高有关。
OA 早期软骨下骨超微结构变化早于显微镜下软骨退变,可能进一步损害关节软骨。这可能与成骨细胞分化水平升高有关。