Inhibition of clathrin/dynamin-dependent internalization interferes with LPS-mediated TRAM-TRIF-dependent signaling pathway

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• 作者：Yanyan Wang^a ; ^c ; ¹ ; Yang Yang^a ; ¹ ; Xin Liu^a ; Ning Wang^a ; Hongwei Cao^a ; Yongling Lu^a ; Hong Zhou^b ; ^{zhouh64@163.com} ; Jiang Zheng^a ; ^{zhengj99219@gmail.com}
• 关键词：LPS ; TLR4 ; Internalization ; MDC ; Dynasore ; Chloroquine ; Cytokines ; Chemokines ; TRAM&ndash ; TRIF-dependent pathway ; MyD88-dependent pathway
• 刊名：Cellular Immunology
• 出版年：2012
• 期刊代码：279_00088749
• 类别：med
• 出版时间：2012
• 卷：274
• 期：1-2
• 页码：121-129
• 文件大小：663 K

摘要

Recognition of lipopolysaccharide (LPS) by Toll-like receptor 4 (TLR4) activates two district proinflammatory signaling pathway and initiates LPS internalization. To investigate roles of LPS internalization, a traditionally regarded metabolic pathway for LPS, in regulation of these two pathways, three internalization inhibitors, monodansylcadaverine (MDC, a clathrin inhibitor), dynasore (DS, a dynamin inhibitor) and chloroquine (CQ, an endosome acidifying maturation inhibitor) were applied to induce internalization dysfunction in macrophages. Results showed MDC and DS affected LPS internalization but did not interfere with their colocalization. Additionally, they decreased cytokines and chemokines release and inhibited signaling molecules activation mediated by TRAM-TRIF-dependent pathway as determined by protein array. In contrast, CQ did not inhibit LPS internalization but affected the colocalization. It also suppressed macrophage activation mediated by both MyD88-dependent and TRAM-TRIF-dependent pathways. The above data indicated that LPS internalization was clathrin/dynamin dependent and it was essential for activation of TRAM-TRIF-dependent signaling pathway.