Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, William Henry Duncan Building, West Derby Street, Liverpool, L7 8TX, UK.
Department of Cellular and Molecular Physiology, Institute of Translational Medicine, University of Liverpool, Nuffield Building, Crown Street, Liverpool, L69 3BX, UK.
Sci Rep. 2019 Aug 1;9(1):11188. doi: 10.1038/s41598-019-47545-2.
The structure, ultrastructure and function of hyaline articular cartilage (HAC) and subchondral bone (SCB), and their involvement in the pathogenesis of osteoarthritis (OA) have been extensively researched. However, much less attention has been focused on the intervening tissue, articular calcified cartilage (ACC) and its role in the initiation and progression of OA. Using both light microscopy (LM) and transmission electron microscopy (TEM), a study of ACC in wild type (WT) mice, and mice with genetic osteoarthropathies (AKU) was undertaken to further understand the role played by ACC in the early stages of OA.Tibio-femoral joints were obtained from BALB/c WT and BALB/c AKU mice aged between 7 and 69 weeks. One joint was processed for routine histological analysis. The tip of the medial femoral condyle (MFC), which contained HAC, ACC, and SCB, was dissected from the contra-lateral joint and processed for TEM.In WT and AKU mice novel microanatomical structures, designated concentric lamellae, were identified surrounding chondrocytes in the ACC. The lamellae appeared to be laid down in association with advancement of the tidemark indicating they may be formed during calcification of cartilage matrix. The lamellae were associated with hypertrophic chondrocytes throughout the ACC.Novel microanatomical structures, termed concentric lamellae, which were present around hypertrophic chondrocytes in the ACC are described for the first time. Their apparent association with mineralisation, advancement of the tidemark, and greater abundance in a model of osteoarthropathy indicate their formation could be important in the pathogenesis of OA and AKU.
关节透明软骨(HAC)和软骨下骨(SCB)的结构、超微结构和功能及其在骨关节炎(OA)发病机制中的作用已经得到了广泛的研究。然而,人们对关节间组织,即关节钙化软骨(ACC)及其在 OA 发病和进展中的作用的关注要少得多。本研究通过使用光学显微镜(LM)和透射电子显微镜(TEM)对野生型(WT)小鼠和具有遗传性骨关节炎(AKU)的小鼠的 ACC 进行了研究,以进一步了解 ACC 在 OA 早期阶段所起的作用。从 7 至 69 周龄的 BALB/c WT 和 BALB/c AKU 小鼠中获取胫股关节。一个关节用于常规组织学分析。从对侧关节中解剖出包含 HAC、ACC 和 SCB 的内侧股骨髁(MFC)尖端,并进行 TEM 处理。在 WT 和 AKU 小鼠中,在 ACC 中的软骨细胞周围发现了新型微解剖结构,命名为同心层。这些层似乎是随着潮线的推进而沉积的,表明它们可能是在软骨基质钙化过程中形成的。这些层与整个 ACC 中的肥大软骨细胞有关。本文首次描述了在 ACC 中的肥大软骨细胞周围存在的新型微解剖结构,称为同心层。它们与矿化、潮线的推进以及在骨关节炎模型中更丰富的存在明显相关,表明它们的形成可能在 OA 和 AKU 的发病机制中很重要。