首页> 外文期刊>Arthritis Research >Cytokine signaling-1 suppressor is inducible by IL-1beta and inhibits the catabolic effects of IL-1beta in chondrocytes: its implication in the paradoxical joint-protective role of IL-1beta
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Cytokine signaling-1 suppressor is inducible by IL-1beta and inhibits the catabolic effects of IL-1beta in chondrocytes: its implication in the paradoxical joint-protective role of IL-1beta

机译:IL-1beta可诱导细胞因子信号传导1抑制剂,并抑制软骨细胞中IL-1beta的分解代谢作用:暗示其与IL-1beta的反常关节保护作用有关

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Introduction Although IL-1β is believed to be crucial in the pathogenesis of osteoarthritis (OA), the IL-1β blockade brings no therapeutic benefit in human OA and results in OA aggravation in several animal models. We explored the role of a cytokine signaling 1 (SOCS1) suppressor as a regulatory modulator of IL-1β signaling in chondrocytes. Methods Cartilage samples were obtained from patients with knee OA and those without OA who underwent surgery for femur-neck fracture. SOCS1 expression in cartilage was assessed with immunohistochemistry. IL-1β-induced SOCS1 expression in chondrocytes was analyzed with quantitative polymerase chain reaction and immunoblot. The effect of SOCS1 on IL-1β signaling pathways and the synthesis of matrix metalloproteinases (MMPs) and aggrecanase-1 was investigated in SOCS1-overexpressing or -knockdown chondrocytes. Results SOCS1 expression was significantly increased in OA cartilage, especially in areas of severe damage ( P
机译:引言尽管人们认为IL-1β在骨关节炎(OA)的发病机理中至关重要,但IL-1β阻断剂对人OA没有任何治疗作用,在几种动物模型中都会导致OA恶化。我们探讨了细胞因子信号传导1(SOCS1)抑制剂作为软骨细胞中IL-1β信号传导的调控因子的作用。方法对膝骨关节炎和非骨关节炎患者行股骨颈骨折手术,取软骨样品。用免疫组织化学评估软骨中SOCS1的表达。用定量聚合酶链反应和免疫印迹法分析IL-1β诱导的软骨细胞SOCS1表达。研究了SOCS1对IL-1β信号通路以及基质金属蛋白酶(MMP)和聚集蛋白聚糖酶1合成的影响。结果OA软骨中SOCS1的表达显着增加,特别是在严重损伤的区域中(P <?0.01)。 IL-1β以剂量依赖的方式刺激SOCS1 mRNA表达(P <?0.01)。 IL-1β诱导的MMP-1,MMP-3,MMP-13和ADAMTS-4(aggrecanase-1,一种具有血小板反应蛋白基序4的解整合素和金属蛋白酶)的生产受到SW1353细胞和原代人关节软骨细胞(所有P值均 0.05)。 SOCS1的抑制作用是通过阻断p38,c-Jun N末端激酶(JNK)和核因子κB(NF-κB)激活,以及下调转化生长因子-β-激活的激酶1(TAK1)的表达而介导的。结论我们的结果表明SOCS1被OA软骨细胞中的IL1-β诱导,并通过在多个水平上抑制IL-1β信号传导来抑制IL-1β诱导的基质降解酶的合成。这表明IL-1β诱导的SOCS1充当OA软骨中IL-1β反应的负调节剂。

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