Arthritis Research UK Centre for OA Pathogenesis, Kennedy Institute of Rheumatology, University of Oxford, Oxford, UK.
J Physiol. 2019 Mar;597(5):1271-1281. doi: 10.1113/JP275451. Epub 2018 Jul 29.
The articular cartilage is exquisitely sensitive to mechanical load. Its structure is largely defined by the mechanical environment and destruction in osteoarthritis is the pathophysiological consequence of abnormal mechanics. It is often overlooked that disuse of joints causes profound loss of volume in the articular cartilage, a clinical observation first described in polio patients and stroke victims. Through the 1980s, the results of studies exploiting experimental joint immobilisation supported this. Importantly, this substantial body of work was also the first to describe metabolic changes that resulted in decreased synthesis of matrix molecules, especially sulfated proteoglycans. The molecular mechanisms that underlie disuse atrophy are poorly understood despite the identification of multiple mechanosensing mechanisms in cartilage. Moreover, there has been a tendency to equate cartilage loss with osteoarthritic degeneration. Here, we review the historic literature and clarify the structural, metabolic and clinical features that clearly distinguish cartilage loss due to disuse atrophy and those due to osteoarthritis. We speculate on the molecular sensing pathways in cartilage that may be responsible for cartilage mechanoadaptation.
关节软骨对机械负荷非常敏感。其结构在很大程度上由机械环境决定,骨关节炎的破坏是力学异常的病理生理后果。人们常常忽视关节的废用会导致关节软骨体积的明显丧失,这一临床观察最早在小儿麻痹症患者和中风患者中描述。直到 20 世纪 80 年代,利用实验性关节固定的研究结果支持了这一观点。重要的是,这项大量的工作也是第一个描述导致基质分子合成减少的代谢变化的研究,尤其是硫酸软骨素蛋白聚糖。尽管在软骨中已经鉴定出多种机械敏感机制,但仍不清楚导致废用性萎缩的分子机制。此外,人们倾向于将软骨丧失等同于骨关节炎的退化。在这里,我们回顾了历史文献,并阐明了结构、代谢和临床特征,这些特征清楚地区分了由于废用性萎缩和骨关节炎引起的软骨丧失。我们推测软骨中的分子感应途径可能是导致软骨力学适应性的原因。