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作 者:蒋明[1] 王昌明[1] 韩旭惠 杨丹[1] 马礼兵[1] 陈峰[1] 吕倩[1]
机构地区:[1]桂林医学院附属医院呼吸内科,广西桂林541001
出 处:《郑州大学学报(医学版)》2017年第5期641-644,共4页Journal of Zhengzhou University(Medical Sciences)
基 金:国家自然科学基金资助项目81360010;广西省卫生厅自然科学基金资助项目S201603
摘 要:目的:探讨慢性阻塞性肺疾病(COPD)大鼠远端原代肺动脉平滑肌细胞(PASMCs)中单核细胞趋化蛋白-1(MCP-1)、转化生长因子-β1(TGF-β1)的分泌情况及其与Toll样受体4(TLR4)信号通路的相关性。方法:通过脂多糖(LPS)诱导建立大鼠COPD模型,分离培养、鉴定原代大鼠PASMCs,以LPS诱导PASMCs,然后分组(对照组、LPS组、TAK-242组,LPS+TAK-242组)培养细胞,用Western blot法检测各组PASMCs中TLR4的表达,ELISA法检测细胞培养上清液MCP-1、TGF-β1的浓度,并进行相关性分析。结果:LPS组较对照组PASMCs中TLR4的表达水平上调(P<0.05),细胞培养上清液中MCP-1、TGF-β1的含量升高(P<0.05);TAK-242组PASMCs中TLR4的表达水平下调(P<0.05),上清液中MCP-1、TGF-β1与TLR4无相关性。结论:LPS可诱导大鼠原代PASMCs合成分泌MCP-1、TGF-β1,同时上调TLR4表达水平。Aim: To probe into the secretion of monocyte chemoattractant protein 1( MCP-1),transforming growth factor β1( TGF-β1) in primary pulmonary artery smooth muscle cells( PASMCs) of chronic obstructive pulmonary disease( COPD) rats and the correlation with toll-like receptor 4( TLR4) signaling pathways. Methods: The COPD rat model was established,and the PASMCs were separated,induced by LPS,and then divided into control group,LPS group,TAK-242 group,and LPS + TAK-242 group. The expression of TLR4 in PASMCs of each group was detected by Western blot,and the concentrations of MCP-1 and TGF-β1 in cell culture fluid were determined by ELISA,and at last a correlation analysis was conducted. Results: In contrast with the control group,the expression of TLR4 in PASMCs of the LPS group was inecreased( P〈0. 05) and the concentrations of MCP-1 and TGF-β1 in cell culture fluid were increased( P〈0. 05). The expression of TLR4 in PASMCs of the TAK-242 group was down-regulated( P〈0. 05) and the concentrations of MCP-1 and TGF-β1 in cell culture fluid showed no correlation with the expression of TLR4. Conclusion: LPS can induce PASMCs of rats to synthesize and secrete MCP-1 and TGF-β1,and the TLR4 is up-expressed at the same time.
关 键 词:慢性阻塞性肺疾病 TOLL样受体4 单核细胞趋化蛋白-1 转化生长因子-Β1 大鼠
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