Lund University, Faculty of Medicine, Department of Clinical Sciences Lund, Orthopaedics, Clinical Epidemiology Unit, Lund, Sweden; Lund University, Faculty of Medicine, Department of Clinical Sciences Lund, Rheumatology and Molecular Skeletal Biology, Lund, Sweden.
Lund University, Faculty of Medicine, Department of Clinical Sciences Lund, Orthopaedics, Clinical Epidemiology Unit, Lund, Sweden.
Osteoarthritis Cartilage. 2020 Aug;28(8):1092-1101. doi: 10.1016/j.joca.2020.05.001. Epub 2020 May 11.
Recent research in knee osteoarthritis (OA) highlights the role of the meniscus in OA pathology. Our aim was to compare the proteomes of medial and lateral menisci from end-stage medial compartment knee OA patients, with reference menisci from knee-healthy deceased donors, using mass spectrometry.
Tissue plugs of Ø3 mm were obtained from the posterior horns of the lateral and medial menisci from one knee of 10 knee-healthy deceased donors and 10 patients undergoing knee replacement. Proteins were extracted and prepared for mass spectrometric analysis. Statistical analysis was conducted on abundance data that was log-transformed, using a linear mixed effects model and evaluated using pathway analysis.
We identified a total of 835 proteins in all samples, of which 331 were included in the statistical analysis. The largest differences could be seen between the medial menisci from OA patients and references, with most proteins showing higher intensities in the medial menisci from OA patients. Several matrix proteins, e.g., matrix metalloproteinase 3 (MMP3) (4.3 times higher values [95%CI 1.8, 10.6]), TIMP1 (3.5 [1.4, 8.5]), asporin (4.1 [1.7, 10.0]) and versican (4.4 [1.8, 10.9]), all showed higher abundance in medial menisci from OA patients compared to medial reference menisci. OA medial menisci also showed increased activation of several pathways involved in inflammation.
An increase in protein abundance for proteins such as MMP and TIMP1 in the medial menisci from OA patients suggests simultaneous activation of both catabolic and anabolic processes that warrants further attention.
最近对膝关节骨关节炎(OA)的研究强调了半月板在 OA 病理中的作用。我们的目的是使用质谱法比较终末期内侧间室膝 OA 患者的内侧和外侧半月板与健康膝关节捐献者参考半月板的蛋白质组。
从 10 名健康膝关节捐献者和 10 名接受膝关节置换术的患者的一个膝关节的外侧和内侧半月板的后角获得 Ø3mm 的组织塞。提取蛋白质并进行质谱分析。对经对数转换的丰度数据进行统计分析,使用线性混合效应模型,并通过途径分析进行评估。
我们在所有样本中总共鉴定出 835 种蛋白质,其中 331 种蛋白质包含在统计分析中。OA 患者的内侧半月板和参考之间的差异最大,大多数蛋白质在 OA 患者的内侧半月板中的强度更高。几种基质蛋白,例如基质金属蛋白酶 3(MMP3)(高 4.3 倍[95%CI 1.8,10.6])、TIMP1(3.5 [1.4,8.5])、asporin(4.1 [1.7,10.0])和 versican(4.4 [1.8,10.9]),在 OA 患者的内侧半月板中均显示出比内侧参考半月板更高的丰度。OA 内侧半月板还显示出几个涉及炎症的途径的激活增加。
OA 患者内侧半月板中 MMP 和 TIMP1 等蛋白的蛋白丰度增加表明同时激活了分解代谢和合成代谢过程,这值得进一步关注。