XAF1 contributes to dengue virus-induced apoptosis in vascular endothelial cells

被引:25
作者
Long, Xigui [1 ,3 ]
Li, Ying [1 ,3 ]
Qi, Yiming [1 ,3 ]
Xu, Juan [1 ,3 ]
Wang, Zilian [2 ]
Zhang, Ximeng [1 ,3 ]
Zhang, Duoduo [1 ,3 ]
Zhang, Lin [1 ,3 ]
Huang, Junqi [1 ,3 ]
机构
[1] Sun Yat Sen Univ, Zhongshan Sch Med, Inst Immunol, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 1, Guangzhou 510080, Guangdong, Peoples R China
[3] Minist Educ, Key Lab Trop Dis Control, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
XIAP; VECs; X-LINKED INHIBITOR; COLON-CANCER; KAPPA-B; INFECTION; GENE; EXPRESSION; PATHWAY; TRAIL; ALPHA; XIAP;
D O I
10.1096/fj.12-213967
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mechanism of vascular leakage in severe dengue infection remains unclear. Here, we used primary human umbilical vein endothelial cells (HUVECs) and the EA.hy926 cell line to study the molecular events that occur after dengue virus serotype 2 (DENV2) infection. DENV2-induced apoptosis was confirmed using nuclear staining, TUNEL assay, and electron microscopy. A genome-wide transcriptome analysis was performed using a microarray of DENV2-infected HUVECs. Notably, interferon-inducible genes were differentially expressed after DENV2 infection. Prominent among these genes was the X chromosome-linked inhibitor of apoptosis protein (XIAP)-associated factor 1 (XAF1; up-regulated 1.2-fold in the microarray analysis and similar to 8-fold by qRT-PCR after DENV2 infection). XAF1 protein levels were up-regulated after DENV2 infection in both HUVECs and EA.hy926 cells. Evidence indicated interaction between XAF1 and XIAP during DENV2 infection based on their cellular localization, as observed by confocal microscopy and the coimmunoprecipitation of XIAP with an anti-XAF1 antibody. Next, recombinant EA.hy926 cell lines in which XAF1 was either knocked down or overexpressed were constructed. The expression levels of the apoptosis-related genes caspase 3, caspase 8, caspase 9, and poly-(ADP-ribose) polymerase (PARP) were down-regulated in the XAF1 knockdown (24-48 h postinfection) but were up-regulated in XAF1 overexpressing cells (36 h postinfection). This is the first study of the role of XAF1 in promoting apoptosis in vascular endothelial cells after DENV2 infection.-Long, X., Li, Y., Qi, Y., Xu, J., Wang, Z., Zhang, X., Zhang, D., Zhang, L., Huang, J. XAF1 contributes to dengue virus-induced apoptosis in vascular endothelial cells. FASEB J. 27, 1062-1073 (2013). www.fasebj.org
引用
收藏
页码:1062 / 1073
页数:12
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