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首页> 外文期刊>International journal of molecular medicine >Involvement of mitogen-activated protein kinases and peroxisome proliferator-activated receptor γ in monosodium urate crystal-induced vascular cell adhesion molecule 1 expression in human rheumatoid arthritis synovial fibroblasts
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Involvement of mitogen-activated protein kinases and peroxisome proliferator-activated receptor γ in monosodium urate crystal-induced vascular cell adhesion molecule 1 expression in human rheumatoid arthritis synovial fibroblasts

机译:丝裂素激活的蛋白激酶和过氧化物酶体增殖物激活的受体γ参与人风湿性关节炎滑膜成纤维细胞尿酸一钠晶体诱导的血管细胞粘附分子1表达

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摘要

To investigate whether monosodium urate (MSU) crystals could induce the production of VCAM-1 (vascular cell adhesion molecule 1) in human synovial cells and its possible signaling pathways, human synovial cells isolated from synovial tissue explants were stimulated with various doses of MSU crystals for different time intervals. Expression of VCAM-1 was evaluated with Western blotting. To explore the underlying mechanisms, VCAM-1 protein expression was also evaluated after activation of several signaling molecules including mitogen-activated protein kinases (MAPKs) and peroxisome proliferator-activated receptor γ (PPARγ) were blocked. Exposure of synovial cells to MSU crystals induced VCAM-1 expression in culture medium in a dose- and time-dependent manner, reaching a plateau at 1000 μM and 24 h. Inhibition of the activation of MAPKs and PPARγ could block this increase. The present results demonstrated that MSU crystals could induce VCAM-1 expression. MAPKs and PPARγ signaling pathways regulated the induced VCAM-1 expression.
机译:为了研究尿酸单钠(MSU)晶体是否能诱导人滑膜细胞中VCAM-1(血管细胞粘附分子1)的产生及其可能的信号通路,用不同剂量的MSU晶体刺激从滑膜组织外植体分离的人滑膜细胞。不同的时间间隔。用蛋白质印迹法评估VCAM-1的表达。为了探索潜在的机制,在阻断包括促分裂原激活蛋白激酶(MAPK)和过氧化物酶体增殖物激活受体γ(PPARγ)在内的几种信号分子激活后,还评估了VCAM-1蛋白的表达。滑膜细胞暴露于MSU晶体会诱导VCAM-1在培养基中的表达,呈剂量和时间依赖性,在1000μM和24 h达到稳定水平。抑制MAPK和PPARγ的激活可以阻止这种增加。目前的结果表明,MSU晶体可以诱导VCAM-1表达。 MAPK和PPARγ信号通路调节诱导的VCAM-1表达。

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