Identification of Serum Biomarkers for Early-Stage Knee Osteoarthritis Using Proteomics in a Murine Model of Osteoarthritis

骨关节炎 医学 内侧半月板 内科学 病理 内分泌学 替代医学
作者
Shohei Yamauchi,Eiji Sasaki,Yota Tatara,K. Ishíbashi,Takahiro Tsushima,Yuka Kimura,Eiichi Tsuda,Yasuyuki Ishibashi
出处
期刊:Cartilage [SAGE Publishing]
标识
DOI:10.1177/19476035251363443
摘要

Objective To characterize the serum protein profiles of osteoarthritis model mice, particularly mice with early-stage osteoarthritis, using liquid chromatography-mass spectrometry (LC-MS/MS). Design Serum and knee samples were collected from 5 control mice and 15 osteoarthritis model mice that underwent destabilization of the medial meniscus (DMM). Osteoarthritic knee samples were collected 4, 8, and 12 weeks after DMM. Knee osteoarthritis severity was scored using the Osteoarthritis Research Society International (OARSI) scoring system. All serum samples were analyzed via LC-MS/MS after removing highly abundant proteins using a ProteoMiner kit (Bio-Rad). Results The average OARSI scores of the medial tibial plateau and medial femoral condyle at 8 weeks after DMM (3.40 ± 1.02 points, P = 0.03; 2.60 ± 1.71 points, P = 0.03) and 12 weeks after DMM (8.30 ± 3.12 points, P = 0.03; 4.80 ± 0.75 points, P = 0.03) were significantly higher than the corresponding values in the control group. Compared to those in the control model, 15, 35, and 56 proteins showed different expression levels at 4, 8, and 12 weeks after DMM, respectively. Differentially expressed proteins at 4 weeks after DMM included adenylate kinase, type IV intermediate filament protein, nestin, and insulin-like growth factor-binding proteins. The pathways activated at 4 weeks after DMM differed from those activated at 8 and 12 weeks after DMM. Conclusion Protein expression and activation pathways in the osteoarthritis model differed from those in the control model. Several proteins differentially expressed at 4 weeks postoperatively may be involved in the pathogenesis of osteoarthritis and serve as potential biomarkers of early-stage osteoarthritis.
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