炎症
软骨细胞
化学
CTL公司*
基质金属蛋白酶
透明质酸
氧化应激
活性氧
活力测定
巨噬细胞炎性蛋白
体外
免疫学
巨噬细胞
生物
趋化因子
生物化学
细胞毒性T细胞
遗传学
作者
Elena Tarricone,Elena Mattiuzzo,Elisa Belluzzi,Rossella Elia,Andrea Benetti,Rina Venerando,Vincenzo Vindigni,Pietro Ruggieri,Paola Brun
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2020-05-26
卷期号:9 (6): 1328-1328
被引量:38
摘要
The development and progression of osteoarthritis (OA) is associated with macrophage-mediated inflammation that generates a broad spectrum of cytokines and reactive oxygen species (ROS). This study investigates the effects of mid-MW hyaluronic acid (HA) in combination with a lactose-modified chitosan (CTL), on pro-inflammatory molecules and metalloproteinases (MMPs) expression, using an in vitro model of macrophage-mediated inflammation. Methods. To assess chondrocyte response to HA and CTL in the presence of macrophage derived inflammatory mediators, cells were exposed to the conditioned medium (CM) of U937 activated monocytes and changes in cell viability, pro-inflammatory mediators and MMPs expression or ROS generation were analysed. Results. CTL induced changes in chondrocyte viability that are reduced by the presence of HA. The CM of activated U937 monocytes (macrophages) significantly increased gene expression of pro-inflammatory molecules and MMPs and intracellular ROS generation in human chondrocyte cultures. HA, CTL and their combinations counteracted the oxidative damage and restored gene transcription for IL-1β, TNF-α, Gal-1, MMP-3 and MMP-13 to near baseline values. Conclusions. This study suggests that HA-CTL mixture attenuated macrophage-induced inflammation, inhibited MMPs expression and exhibited anti-oxidative effects. This evidence provides an initial step toward the development of an early stage OA therapeutic treatment
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