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Acute Synovitis after Trauma Precedes and is Associated with Osteoarthritis Onset and Progression

机译:创伤后急性滑膜炎术后,与骨关节炎发病和进展相关

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Osteoarthritis (OA) is a whole-joint disease characterized by cartilage destruction, subchondral bone sclerosis, osteophyte formation, and synovitis. However, it remains unclear which part of the joint undergoes initial pathological changes that drives OA onset and progression. In the present study, we investigated the longitudinal alterations of the entire knee joint using a surgically-induced OA mouse model. Histology analysis showed that synovitis occurred as early as 1 week after destabilization of the medial meniscus (DMM), which preceded the events of cartilage degradation, subchondral sclerosis and osteophyte formation. Importantly, key pro-inflammatory cytokines such as IL-1β, IL-6, TNFα, and Ccl2, major matrix degrading enzymes including Adamts4, Mmp3 and Mmp13, as well as nerve growth factor (NGF), all increased significantly in both synovium and articular cartilage. It is notable that the inductions of these factors in synovium are far more extensive than those in articular cartilage. Results from behavioral tests demonstrated that sensitization of knee joint pain developed after 8 weeks, later than histological and molecular changes. In addition, the nanoindentation modulus of the medial tibiae decreased 4 weeks after DMM surgery, simultaneous with histological OA signs, which is also later than appearance of synovitis. Collectively, our data suggested that synovitis precedes and is associated with OA, and thus synovium may be an important target to intervene in OA treatment.? The author(s).
机译:骨关节炎(OA)是一种全关节疾病,其特征在于软骨破坏,骨髓性骨硬化,骨赘形成和滑膜炎。然而,仍然不清楚哪个部分接触经历初始的病理变化,驱动OA发作和进展。在本研究中,我们使用手术诱导的OA小鼠模型研究了整个膝关节的纵向改变。组织学分析表明,在内侧弯月面(DMM)的稳定性后1周发生的滑膜炎,其在软骨降解,骨髓性硬化和骨赘形成之前。重要的是,诸如IL-1β,IL-6,TNFα和CCL2的关键促炎细胞因子,主要基质降解酶,包括ADAMTS4,MMP3和MMP13以及神经生长因子(NGF),在两个Synovium和关节软骨。值得注意的是,臂章中这些因素的诱导比关节软骨中的这些因素更广泛。行为试验结果表明,8周后膝关节疼痛的敏化性比组织学和分子变化晚。此外,中介胫骨的纳米茚调模量在DMM手术后4周减少,同时具有组织学OA标志,其也晚于滑膜炎。统称,我们的数据表明,滑膜炎前面并与OA相关,因此Synovium可能是在OA治疗中进行干预的重要靶标。作者。

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