p38 MAPK在嗜酸性粒细胞活化支气管上皮细胞释放MCP1中的作用
上皮细胞,,支气管;上皮细胞;嗜酸细胞;单核细胞化学吸引蛋白质1;p38,MAPK,p38MAPK在嗜酸性粒细胞活化支气管上皮细胞释放MCP1中的作用,0引言,1材料和方法,2结果,3讨论,【
Regulatory role of p38 MAPK for MCP1 release from activated bronchial epithelial cells by eosinophilsWANG ChengBin, TONG HongLi, TIAN YaPing, WANG DeQing, HUANG ZhenGuo, YE WeiJi, LI LuoYi, LIN WeiJi
Department of Clinical Biochemistry, Chinese PLA General Hospital, Beijing 100853, China, Department of Chemical Pathology, Chinese University of Hong Kong, Hong Kong, China
【Abstract】 AIM: To investigate the release of monocyte chemoattractant protein (MCP)1 from the coculture of human bronchial epithelial cells and eosinophils and the related mechanisms. METHODS: MCP1 in culture supernatant was determined by Cytometric Bead Array (CBA) Kit in flow cytometry to compare MCP1 release in bronchial epithelial cells and eosinophils cultured alone or together, and investigate the inhibitive effect of SB 203580, a selective inhibitor of p38 MAPK, on MCP1 release. The reverse transcriptasepolymerase chain reaction (RTPCR) was used to analyze the gene expression of MCP1 in bronchial epithelial cells during coculture with eosinophils and the effect of SB 203580. RESULTS: The interaction of eosinophils and bronchial epithelial cells was found to upregulate the gene expression of MCP1 in epithelial cells. MCP1 in coculture supernatant of bronchial epithelial cells and eosinophils was elevated significantly [(1266±127) ng/L vs (134±25) ng/L,P<0.001]. Fixed eosinophils, which lost the ability to release MCP1, could also elevate epithelial cells to release MCP1 [(773±48) ng/L vs (107±15) ng/L, P<0.001] in coculture. SB 203580 could effectively inhibit MCP1 gene expression of bronchial epithelial cells during coculture with eosinophils, and decreased the release of MCP1 in the coculture of epithelial cells and eosinophils or fixed eosinophils [(1335±115) ng/L vs (481±42) ng/L, (868±89) ng/L vs (239±26) ng/L, P<0.001]. CONCLUSION: Eosinophils can activate bronchial epithelial cells to express MCP1 in coculture by p38 MAPK pathway so as to regulate the airway inflammatory reaction. ......
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