Experimental Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands.
Experimental Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands
Rheumatology (Oxford). 2016 Jan;55(1):16-24. doi: 10.1093/rheumatology/kev270. Epub 2015 Jul 31.
There is increasing evidence that low-density lipoprotein (LDL) cholesterol plays a role in the pathology of OA. Specifically, oxidized LDL (oxLDL), which has been shown to play an essential role during development of atherosclerosis, could be involved in processes such as synovial inflammation, cartilage destruction and bone deformations. OxLDL can activate synovial cells such as macrophages, endothelial cells and synovial fibroblasts, resulting in release of growth factors, MMP and pro-inflammatory cytokines. In this review article, we discuss the role of LDL and oxLDL in OA joint pathology and share our viewpoint of possible mechanisms by which these proteins could influence the development and progression of OA. The proposed theory could provide insight into the aetiopathology of OA and give rise to new potential treatments.
越来越多的证据表明,低密度脂蛋白(LDL)胆固醇在 OA 的病理学中起作用。具体来说,已经表明氧化的 LDL(oxLDL)在动脉粥样硬化的发展过程中起着至关重要的作用,它可能参与诸如滑膜炎、软骨破坏和骨骼畸形等过程。oxLDL 可以激活滑膜细胞,如巨噬细胞、内皮细胞和滑膜成纤维细胞,导致生长因子、MMP 和促炎细胞因子的释放。在这篇综述文章中,我们讨论了 LDL 和 oxLDL 在 OA 关节病理学中的作用,并分享了我们对这些蛋白质可能影响 OA 发展和进展的可能机制的观点。这一理论可以深入了解 OA 的病因学,并为新的潜在治疗方法提供依据。