NHERF1 regulates gp120-induced internalization and signaling by CCR5, and HIV-1 production
Kuang YQ1; Pang W2; Zheng YT2; Dupre DJ[*]1
刊名EUROPEAN JOURNAL OF IMMUNOLOGY
2012
卷号42期号:2页码:299-310
关键词CCR5 gp120 G protein-coupled receptor H plus exchanger regulator factor 1 (NHERF1) Signaling
通讯作者denis.dupre@dal.ca
合作状况其它
英文摘要The scaffolding protein Na+/H+ exchanger regulator factor 1 (NHERF1) plays an important role in the trafficking of G protein-coupled receptors. We previously demonstrated that NHERF1 is involved in chemokine receptor CCR5 homodimer internalization and signal transduction. Given the importance of CCR5 internalization during HIV-1 infection, we evaluated NHERF1's contribution in HIV-1 infection. We challenged human osteosarcoma cells coexpressing CD4 and CCR5 cells expressing either NHERF1 fragment domains or WT NHERF1 with an HIV-1 strain to examine the effects of NHERF1 on HIV-1 entry and replication. WT NHERF1 potentiates HIV-1 envelope gp120-induced CCR5 internalization, and promotes the replication of HIV-1. In order to better understand how NHERF1 affects signal transduction, different domains of NHERF1 were overexpressed in cells to analyze their effect on the different signaling pathways. Here, we show that NHERF1 can associate with CCR5, and promote activation of the gp120-induced MAPK/ERK, focal adhesion kinase and RhoA (Ras homolog gene family member A) signaling pathways. NHERF1 overexpression also increases HIV-1 host cell migration triggered by gp120 via focal adhesion kinase (FAK) signaling. Finally, NHERF1 enhanced actin filament rearrangement in host cells, an important step in post-entry HIV-1 replication events. While postsynaptic density 95/disk-large/zonula occludens 2 (PDZ2) appears to be the major contributor in those events, other domains also participate in the regulation of gp120-induced signaling pathways. Altogether, our results suggest a very important role of the scaffold NHERF1 in the regulation of HIV-1 entry and replication.
收录类别SCI
资助信息This work was partially supported by grants from the Canadian Institutes of Health Research (No. HOP-86863) and NSERC (No. RGPIN/355310-2008) to D.J.D. D.J.D. is the recipient of a CIHR New Investigator Award and Dalhousie Medical Research Foundation New Investigator Award. This work was also partially supported by grants from National Basical Research Program of China (No.2009CB522306), Eleven Five-Year Key Scientific and Technological Program of China (No. 2009ZX09501-029, 2008ZX10001-015, 2008ZX10005-002), and National Natural Science Fundation of China (No. U0832601) to Y.T.Z.
语种英语
WOS记录号WOS:000299337800006
公开日期2012-03-20
内容类型期刊论文
源URL[http://159.226.149.42:8088/handle/353002/6877]  
专题昆明动物研究所_分子免疫药理学
昆明动物研究所_动物模型与人类重大疾病机理重点实验室
作者单位1.Department of Pharmacology, Faculty of Medicine, Dalhousie University, Halifax, NS, Canada
2.Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences and Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, P. R. China
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Kuang YQ,Pang W,Zheng YT,et al. NHERF1 regulates gp120-induced internalization and signaling by CCR5, and HIV-1 production[J]. EUROPEAN JOURNAL OF IMMUNOLOGY,2012,42(2):299-310.
APA Kuang YQ,Pang W,Zheng YT,&Dupre DJ[*].(2012).NHERF1 regulates gp120-induced internalization and signaling by CCR5, and HIV-1 production.EUROPEAN JOURNAL OF IMMUNOLOGY,42(2),299-310.
MLA Kuang YQ,et al."NHERF1 regulates gp120-induced internalization and signaling by CCR5, and HIV-1 production".EUROPEAN JOURNAL OF IMMUNOLOGY 42.2(2012):299-310.
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