Chae Dong-Sik, Kim Mi Eun, Kang Kyung-Yil, Lee Nae Yoon, Lee Woo-Suk, Lee Jun Sik
Department of Orthopedic Surgery, International St. Mary's Hospital, College of Medicine, Catholic Kwandong University, Incheon 22711, Republic of Korea.
Department of Life Science, Immunology Research Lab, BK21-Four Education Research Group, College of Natural Sciences, Chosun University, Gwangju 61452, Republic of Korea.
Exp Ther Med. 2021 Dec;22(6):1470. doi: 10.3892/etm.2021.10905. Epub 2021 Oct 21.
Osteoarthritis (OA), which is caused by joint damage, is the most common form of arthritis, affecting millions of people worldwide. This damage can accumulate over time, which is why aging is one of the main contributors to joint damage associated with OA. The OA-related proteins that have been reported to date have been identified by the comparative analysis of OA patients with normal controls, following surgical or pharmacological treatment. For the first time, the present study analyzed OA-related proteins in patients with OA according to the International Cartilage Repair Society (ICRS) scale. Changes in protein expression can be observed during the OA process. The present study demonstrated differential protein expression patterns in articular cartilage from ICRS1- and ICRS3-graded OA patients. ICRS grade-matched OA knee samples from 12 OA patients, 6 ICRS grade 1 patients and 6 ICRS3 patients were subjected to proteomic analysis using the LTQ-Orbitrap mass spectrometry system. A total of 231 unique proteins were identified as expressed across the ICRS1 and ICRS3 OA patient groups. Relative differences in protein expression associated with the following classifications were observed: Biological adhesion, cell killing, cellular process, development process and molecular function. Although some of these proteins have been previously reported to be associated with rheumatoid arthritis, including cartilage oligomeric matrix protein, collagen types, angiogenin, complement C5 and CD59 glycoprotein, numerous additional proteins were newly identified, which may further help our understanding of disease pathogenesis. These findings suggested that these proteins may be used to develop novel therapeutic targets for OA.
骨关节炎(OA)是由关节损伤引起的,是最常见的关节炎形式,影响着全球数百万人。这种损伤会随着时间的推移而累积,这就是为什么衰老也是与OA相关的关节损伤的主要促成因素之一。迄今为止报道的与OA相关的蛋白质是通过对接受手术或药物治疗后的OA患者与正常对照进行比较分析而确定的。本研究首次根据国际软骨修复协会(ICRS)分级标准分析了OA患者中与OA相关的蛋白质。在OA过程中可以观察到蛋白质表达的变化。本研究展示了ICRS1级和ICRS3级OA患者关节软骨中不同的蛋白质表达模式。来自12例OA患者(6例ICRS 1级患者和6例ICRS 3级患者)的ICRS分级匹配的OA膝关节样本使用LTQ-Orbitrap质谱系统进行了蛋白质组学分析。总共鉴定出231种独特的蛋白质在ICRS1和ICRS3 OA患者组中均有表达。观察到与以下分类相关的蛋白质表达的相对差异:生物黏附、细胞杀伤、细胞过程、发育过程和分子功能。尽管其中一些蛋白质先前已被报道与类风湿性关节炎相关,包括软骨寡聚基质蛋白、胶原类型、血管生成素、补体C5和CD59糖蛋白,但许多其他蛋白质是新发现的,这可能有助于我们进一步了解疾病的发病机制。这些发现表明,这些蛋白质可用于开发针对OA的新型治疗靶点。