蛋白酶激活受体2激动剂诱导上皮细胞分泌MCP1
蛋白酶激活受体,,蛋白酶激活受体;上皮细胞系;单核细胞趋化蛋白1,0引言,1材料和方法,2结果,3讨论,【参考文献】
Induction of secretion of MCP1 from epithelial cells by proteinase activated receptors2 agonistsWANG HaiYan, HE ShaoHeng
Allergy and Inflammation Research Institute, Shantou University Medical College, Shantou 515031, China
【Abstract】 AIM: To investigate the actions of agonists of proteinase activated receptors (PAR)2 on the secretion of monocyte chemoattractant protein1 (MCP1) from human lung epithelial cells. METHODS: A549 cells were cultured in a 12well culture plate. The challenge was performed by adding various concentrations of PAR2 agonists or their reverse peptides into each well, respectively. After 2 h, 8 h or 16 h, the reactions were terminated by removal of the supernatant from each well. A Sandwich ELISA was used to determine the levels of MCP1 in supernatants. RESULTS: Following 16 h incubation, PAR2 agonists SerLeuIleGlyLysValamide (SLIGKV) and transcinnamoylLeuIleGlyArgLeuOrnamide (tcLIGRLO) were able to induce concentration dependent secretion of MCP1. The maximum release of MCP1 was 13 fold more than the baseline release. The reverse PAR2 agonists had little effects on MCP1 release. The time course showed that the actions of PAR2 agonists initiated at 2 h and reached their peaks at 16 h. CONCLUSION: Agonists of PAR2 are potent secretogogues of MCP1 release from cultured human lung epithelial cells. Their antagonists may possess the ability to inhibit airway inflammation. ......
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