Laboratory of Cytogenetics and Molecular Genetics, Faculty of Medicine, University of Thessaly, Larissa, Greece.
Department of Biology, Faculty of Medicine, University of Thessaly, Larissa, Greece.
Mech Ageing Dev. 2022 Dec;208:111730. doi: 10.1016/j.mad.2022.111730. Epub 2022 Sep 7.
Leptin and ROS are implicated in the regulation of inflammatory pathways including NLRP3-inflammasome. We investigated the functional link between leptin, ROS and NLRP3-inflammasome formation/activation in osteoarthritis (OA), an age-related disease. We found that inflammasome components' (NLRP3, ASC, Caspase-1 and cleaved Caspase-1) protein expression were increased in OA cartilage biopsies and chondrocytes compared to healthy cartilage and chondrocytes. Immunofluorescence showed increased co-localization of NLRP3/ASC and NLRP3/Caspase-1, ASC-specks formation and ROS levels in OA compared to normal chondrocytes. NOX4 mRNA expression and IL-1β/IL-18 secretion levels were also elevated in OA chondrocytes. Furthermore, NLRP3-siRNA in OA chondrocytes revealed significant MMP-9/MMP-13 downregulation. To elucidate leptin/ROS/NLRP3-inflammasome interactions, OA chondrocytes were treated with ROS-inhibitor NAC, NOXs-inhibitor DPI, NOX4-inhibitor GLX351322 and leptin-siRNA, while normal chondrocytes were incubated with leptin with or without DPI or GLX351322. We observed attenuated ROS levels and NLRP3-inflammasome formation/activation in NAC-, DPI- or GLX351322-treated OA chondrocytes, while the same effect was shown after transfection with leptin-siRNA. Furthermore, incubation of normal chondrocytes with leptin enhanced ROS production and inflammasome formation/activation, while pretreatment with DPI or GLX351322 abolished leptin's stimulatory effects confirming leptin-NOX4-ROS-inflammasome regulatory axis. Overall, our findings provide novel evidence indicating that leptin-induced NLRP3-inflammasome formation/activation in OA chondrocytes is mediated by NOX4-dependent ROS production.
瘦素和 ROS 参与炎症途径的调节,包括 NLRP3 炎性小体。我们研究了瘦素、ROS 和 NLRP3 炎性小体形成/激活在骨关节炎(OA)中的功能联系,OA 是一种与年龄相关的疾病。我们发现,与健康软骨和软骨细胞相比,OA 软骨活检和软骨细胞中炎性小体成分(NLRP3、ASC、Caspase-1 和 cleaved Caspase-1)的蛋白表达增加。免疫荧光显示,与正常软骨细胞相比,OA 软骨细胞中 NLRP3/ASC 和 NLRP3/Caspase-1 的共定位增加,ASC 斑点形成和 ROS 水平增加。OA 软骨细胞中的 NOX4 mRNA 表达和 IL-1β/IL-18 分泌水平也升高。此外,在 OA 软骨细胞中,NLRP3-siRNA 显著下调 MMP-9/MMP-13。为了阐明瘦素/ROS/NLRP3 炎性小体的相互作用,用 ROS 抑制剂 NAC、NOXs 抑制剂 DPI、NOX4 抑制剂 GLX351322 和瘦素-siRNA 处理 OA 软骨细胞,而用瘦素或 DPI 或 GLX351322 孵育正常软骨细胞。我们观察到 NAC、DPI 或 GLX351322 处理的 OA 软骨细胞中 ROS 水平和 NLRP3 炎性小体的形成/激活减弱,而转染瘦素-siRNA 则表现出相同的效果。此外,在正常软骨细胞中孵育瘦素增强了 ROS 的产生和炎性小体的形成/激活,而用 DPI 或 GLX351322 预处理则消除了瘦素的刺激作用,证实了瘦素-NOX4-ROS 炎性小体调节轴。总的来说,我们的研究结果提供了新的证据,表明瘦素诱导的 OA 软骨细胞中 NLRP3 炎性小体的形成/激活是由 NOX4 依赖性 ROS 产生介导的。