GB virus type C E2 protein inhibits human immunodeficiency virus type 1 Gag assembly by downregulating human ADP-ribosylation factor 1

被引:4
|
作者
Wang, Chenliang [1 ,2 ,3 ,4 ]
Timmons, Christine L. [1 ]
Shao, Qiujia [1 ]
Kinlock, Ballington L. [1 ]
Turner, Tiffany M. [1 ]
Iwamoto, Aikichi [5 ]
Zhang, Hui [2 ,3 ,4 ]
Liu, Huanliang [2 ,3 ,4 ]
Liu, Bindong [1 ]
机构
[1] Meharry Med Coll, Dept Microbiol & Immunol, Ctr AIDS Hlth Dispar Res, Nashville, TN 37208 USA
[2] Sun Yat Sen Univ, Guangdong Prov Key Lab Colorectal & Pelv Floor Di, Guangdong Inst Gastroenterol, Dept Clin Lab, Guangzhou 510275, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Inst Human Virol, Affiliated Hosp 6, Guangzhou 510275, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Key Lab Trop Dis Control, Minist Educ, Guangzhou 510275, Guangdong, Peoples R China
[5] Univ Tokyo, Inst Med Sci, Div Infect Dis, Adv Clin Res Ctr, Tokyo, Japan
基金
美国国家卫生研究院;
关键词
GBV-C E2; HIV-1; assembly; Gag; plasma membrane targeting; ARF1; Immunology and Microbiology Section; Immune response; Immunity; TO-GOLGI TRANSPORT; ENDOPLASMIC-RETICULUM; GLYCOPROTEIN E2; BREFELDIN-A; HIV-1; GAG; ENTRY INHIBITION; PLASMA-MEMBRANE; AMINO-TERMINUS; LIVING CELLS; ARF PROTEINS;
D O I
10.18632/oncotarget.6537
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
GB virus type C (GBV-C) glycoprotein E2 protein disrupts HIV-1 assembly and release by inhibiting Gag plasma membrane targeting, however the mechanism by which the GBV-C E2 inhibits Gag trafficking remains unclear. In the present study, we identified ADP-ribosylation factor 1 (ARF1) contributed to the inhibitory effect of GBV-C E2 on HIV-1 Gag membrane targeting. Expression of GBV-C E2 decreased ARF1 expression in a proteasomal degradation-dependent manner. The restoration of ARF1 expression rescued the HIV-1 Gag processing and membrane targeting defect imposed by GBV-C E2. In addition, GBV-C E2 expression also altered Golgi morphology and suppressed protein traffic through the secretory pathway, which are all consistent with a phenotype of disrupting the function of ARF1 protein. Thus, our results indicate that GBV-C E2 inhibits HIV-1 assembly and release by decreasing ARF1, and may provide insights regarding GBV-C E2's potential for a new therapeutic approach for treating HIV-1.
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页码:43293 / 43309
页数:17
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