Department of Orthopaedics, Peking University Third Hospital, Beijing, China.
State Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, Chinese Academy of Sciences, Beijing, China.
Connect Tissue Res. 2021 Nov;62(6):709-719. doi: 10.1080/03008207.2020.1870969. Epub 2021 Jan 17.
Osteoarthritis (OA) is a joint disorder involving cartilage degeneration and subchondral bone sclerosis. The bone-cartilage interface is implicated in OA pathogenesis due to its susceptibility to mechanical and biological factors. The crosstalk between cartilage and the underlying subchondral bone is elevated in OA due to multiple factors, such as increased vascularization, porosity, microcracks and fissures. Changes in the osteochondral joint are traceable to alterations in chondrocytes and bone cells (osteoblasts, osteocytes and osteoclasts). The phenotypes of these cells can change with the progression of OA. Aberrant intercellular communications among bone cell-bone cell and bone cell-chondrocyte are of great importance and might be the factors promoting OA development. An appreciation of cellular phenotypic changes in OA and the mechanisms by which these cells communicate would be expected to lead to the development of targeted drugs with fewer side effects.
骨关节炎(OA)是一种关节疾病,涉及软骨退化和软骨下骨硬化。由于其易受机械和生物因素的影响,骨-软骨界面与 OA 的发病机制有关。由于多种因素,如血管生成增加、多孔性、微裂纹和裂隙,OA 中软骨和下面的软骨下骨之间的串扰增加。骨软骨关节的变化可归因于软骨细胞和骨细胞(成骨细胞、骨细胞和破骨细胞)的改变。这些细胞的表型可以随着 OA 的进展而改变。骨细胞-骨细胞和骨细胞-软骨细胞之间异常的细胞间通讯非常重要,可能是促进 OA 发展的因素。了解 OA 中细胞表型变化以及这些细胞如何进行通讯的机制,有望开发出副作用更少的靶向药物。