Department of Anesthesiology, Guizhou Medical University, Guiyang, Guizhou 550004, P.R. China.
Department of Pain Medicine, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou 550004, P.R. China.
Mol Med Rep. 2018 Aug;18(2):2110-2116. doi: 10.3892/mmr.2018.9208. Epub 2018 Jun 22.
Degenerative alterations in articular cartilage are involved in the pathogenesis of osteoarthritis. The present study aimed to evaluate the role of complement component 5a (C5a) in osteoarthritic alterations in the articular cartilage and synovialis via a joint immobilization (IM) rat model. Rats were assigned to three groups: Control, IM and IM+anti‑C5a antibody (IM+anti‑C5a) groups. A terminal deoxynucleotidyl transferase dUTP nick end labeling assay and hematoxylin and eosin staining were used to evaluate the morphological alterations in the articular cartilage and synovialis. Reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR) analysis, immunohistochemical analysis and western blotting were used to evaluate C5a expression in the articular cartilage and synovialis. An ELISA was used to evaluate C5a‑induced alterations in interleukin (IL)‑1β, IL‑17A and tumor necrosis factor (TNF)‑α levels in the serum and joint fluid. The results demonstrated that knee joint immobilization induced destruction of knee joint synovial fluid and cartilage in the IM and IM+anti‑C5a antibody groups. Immobilization significantly increased the expression levels of C5a in serum and joint fluid in the IM group. Immunohistochemistry, western blotting and RT‑qPCR analysis illustrated markedly increased expression of C5a in the IM group. Immobilization markedly increased the IL‑1β, IL‑17A and TNF‑α expression levels in the serum and joint fluid in the IM group. Anti‑C5a was able to decrease immobilization‑induced alterations in morphology and cytokines compared with the IM group. The expression of C5a was increased in synoviocytes and joint cartilage in the IM model. Pro‑inflammatory cytokines, including TNF‑α and IL‑1β were released in the activated synoviocytes via the induction of C5a, suggesting that C5a serves an important role in joint inflammatory processes.
关节软骨的退行性改变与骨关节炎的发病机制有关。本研究旨在通过关节固定(IM)大鼠模型评估补体成分 5a(C5a)在关节软骨和滑膜骨关节炎改变中的作用。大鼠分为三组:对照组、IM 组和 IM+抗 C5a 抗体(IM+抗 C5a)组。末端脱氧核苷酸转移酶 dUTP 缺口末端标记法和苏木精和伊红染色用于评估关节软骨和滑膜的形态改变。逆转录-定量聚合酶链反应(RT-qPCR)分析、免疫组织化学分析和 Western blot 用于评估关节软骨和滑膜中 C5a 的表达。ELISA 用于评估 C5a 诱导的血清和关节液中白细胞介素(IL)-1β、IL-17A 和肿瘤坏死因子(TNF)-α水平的改变。结果表明,膝关节固定导致 IM 和 IM+抗 C5a 抗体组的膝关节滑膜液和软骨破坏。固定显著增加了 IM 组血清和关节液中 C5a 的表达水平。免疫组织化学、Western blot 和 RT-qPCR 分析表明,IM 组 C5a 的表达明显增加。固定显著增加了 IM 组血清和关节液中 IL-1β、IL-17A 和 TNF-α的表达水平。与 IM 组相比,抗 C5a 能够降低固定诱导的形态和细胞因子的改变。在 IM 模型中,C5a 在滑膜细胞和关节软骨中的表达增加。TNF-α 和 IL-1β 等促炎细胞因子通过 C5a 的诱导在活化的滑膜细胞中释放,表明 C5a 在关节炎症过程中起重要作用。