Department of Orthopaedics, The Second Hospital of Shanxi Medical University, Shanxi Key Laboratory of Bone and Soft Tissue Injury Repair, Taiyuan, Shanxi, PR China.
Department of Orthopaedics, The Alpert Medical School of Brown University, Providence, RI, USA.
Int Immunopharmacol. 2018 Dec;65:212-220. doi: 10.1016/j.intimp.2018.10.007. Epub 2018 Oct 11.
BACKGROUND: It has been noted that anterior cruciate ligament (ACL) injury-induced cartilage degeneration is the key risk factor for post-traumatic osteoarthritis (PTOA). However, whether the cartilage degeneration after ACL injury is caused by inflammation, abnormal biomechanics or both remains largely unknown, as there has been no animal model for separating the two factors so far. METHODS: Eighteen-month-old female mini-pigs were divided into an "idealized" anterior cruciate ligament reconstruction (IACLR) group and a control group (n = 16 limbs per group). Real-time PCR, safranine O staining and indian ink staining were performed to verify whether animal models were successfully established or not. Multiple linear regression analysis was used to evaluate the correlation between levels of the inflammatory factors (including interferon [IFN]-γ, interleukin [IL]-1β, IL-4, IL-6, IL-8, IL-10, IL-12 and tumor necrosis factor [TNF]-α measured by the Luminex method) and changes in cartilage histology (quantified by morphological scoring) after surgery. RESULTS: A significant OA cartilage damage with increased MMP-1, MMP-13 mRNA levels and reduced aggrecan mRNA/protein levels was observed in IACLR groups. As a result, the IACLR gross morphology score was dramatically increased than control. Moreover, IACLR significantly increased the levels of IL-1β, IL-4, IL-6 and TNF-α in the synovial fluid of the knee. Most importantly, a close relationship was found between IL-1β, IL-6 and TNF-α concentrations and morphological score of PTOA, respectively. CONCLUSION: These results demonstrated that inflammatory factors are independently responsible for the onset of PTOA.
背景:研究表明,前交叉韧带(ACL)损伤导致的软骨退变是创伤后骨关节炎(PTOA)的关键风险因素。然而,ACL 损伤后软骨退变是由炎症、异常生物力学还是两者共同引起的,目前仍知之甚少,因为到目前为止还没有一种动物模型可以将这两个因素分开。
方法:将 18 月龄雌性小型猪分为理想化前交叉韧带重建(IACLR)组和对照组(每组 16 个肢体)。采用实时 PCR、番红 O 染色和印度墨水染色来验证动物模型是否成功建立。采用多元线性回归分析来评估炎症因子(通过 Luminex 方法测量的干扰素[IFN]-γ、白细胞介素[IL]-1β、IL-4、IL-6、IL-8、IL-10、IL-12 和肿瘤坏死因子[TNF]-α)水平与术后软骨组织学变化(通过形态学评分定量)之间的相关性。
结果:在 IACLR 组中,观察到明显的 OA 软骨损伤,伴有 MMP-1、MMP-13 mRNA 水平升高和聚集蛋白聚糖 mRNA/蛋白水平降低。结果,IACLR 大体形态评分明显高于对照组。此外,IACLR 显著增加了膝关节滑液中 IL-1β、IL-4、IL-6 和 TNF-α的水平。最重要的是,发现 IL-1β、IL-6 和 TNF-α浓度与 PTOA 的形态评分之间存在密切关系。
结论:这些结果表明,炎症因子是 PTOA 发病的独立因素。
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