Immunology and Molecular Biology Department, Nasonova Research Institute of Rheumatology, 34A Kashirskoye shosse, Moscow, 115522, Russia.
Rheumatol Int. 2018 Nov;38(11):1963-1974. doi: 10.1007/s00296-018-4103-4. Epub 2018 Jul 17.
Osteoarthritis (OA) is a chronic disorder associated mainly with pain, limited range of motion, stiffness, low-grade systemic inflammation, and articular cartilage destruction. Recent studies have demonstrated the involvement of chondrocyte differentiation (hypertrophy) as one of the mechanisms in cartilage degradation in OA. This implicates the involvement of principal changes in the regulation of cellular function associated with profound alterations in chondrocyte energy metabolism in the course of cartilage resorption. Therefore, this review describes the major energy-generating pathways and their regulatory molecules used by the growth plate chondrocytes during endochondral ossification and by articular chondrocytes in OA. These regulatory molecules facilitate either the glycolytic pathway of energy generation, which controls cell proliferation, or mitochondrial oxidative phosphorylation promoted by AMPK and sirtuins and responsible for tissue regeneration. Consideration of the disturbances in energy metabolic pathways associated with OA might provide an approach to disclose the primary causes of the disease's development and progression. Medline/PubMed was searched for publications in English using key words: osteoarthritis, epiphyseal growth plate, articular cartilage, glycolysis, oxidative phosphorylation, and regulation of energy metabolism.
骨关节炎(OA)是一种主要与疼痛、运动范围受限、僵硬、低度全身炎症和关节软骨破坏相关的慢性疾病。最近的研究表明,软骨细胞分化(肥大)是 OA 中软骨降解的机制之一。这意味着在软骨吸收过程中,与软骨细胞能量代谢的深刻改变相关的细胞功能调节的主要变化的参与。因此,本综述描述了生长板软骨细胞在软骨内成骨过程中和关节软骨细胞在 OA 中使用的主要能量产生途径及其调节分子。这些调节分子促进控制细胞增殖的糖酵解途径,或由 AMPK 和 Sirtuins 促进的线粒体氧化磷酸化,负责组织再生。考虑与 OA 相关的能量代谢途径的紊乱可能为揭示疾病发展和进展的主要原因提供一种方法。使用关键词:骨关节炎、骺板、关节软骨、糖酵解、氧化磷酸化和能量代谢调节,在 Medline/PubMed 上搜索英文出版物。