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瘦素依赖的 NLRP3 炎性小体在骨关节炎软骨细胞中的激活是由 ROS 介导的。

Leptin-depended NLRP3 inflammasome activation in osteoarthritic chondrocytes is mediated by ROS.

机构信息

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.

出版信息

Mech Ageing Dev. 2022 Dec;208:111730. doi: 10.1016/j.mad.2022.111730. Epub 2022 Sep 7.

Abstract

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.

摘要

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。

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