IFIT1 Expression Patterns Induced by H9N2 Virus and Inactivated Viral Particle in Human Umbilical Vein Endothelial Cells and Bronchus Epithelial Cells

被引:13
|
作者
Feng, Bo [1 ,2 ]
Zhang, Qian [1 ,2 ]
Wang, Jianfang [1 ]
Dong, Hong [1 ]
Mu, Xiang [1 ]
Hu, Ge [1 ]
Zhang, Tao [1 ]
机构
[1] Beijing Univ Agr, Coll Anim Sci & Technol, Beijing Key Lab Tradit Chinese Vet Med, Beijing 102206, Peoples R China
[2] China Agr Univ, Coll Vet Med, Dept Pathophysiol, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
endothelial cells; H9N2; virus; IFIT1 expression pattern; IFN-alpha/beta; AVIAN INFLUENZA-VIRUSES; INTERFERON-STIMULATED GENES; LOWER RESPIRATORY-TRACT; H5N1; VIRUS; A VIRUS; INFECTION; INDUCTION; REPLICATION; PROTEINS; DISTINCT;
D O I
10.14348/molcells.2018.2091
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
IFIT1 (also known as ISG56) is a member of the interferon-inducible protein with tetratricopeptide repeats (IFITs) family. IFITs are strongly induced by type I interferon (IFN), double-stranded RNA and virus infection. Here, we investigated IFIT1 expression in human umbilical vein endothelial cells (HUVECs) and in human bronchus epithelial cells (BEAS-2Bs) induced by the H9N2 virus and inactivated viral particle at different time points. We also investigated the effect of H9N2 virus and viral particle infection on IFN-alpha/beta production, and assessed whether hemagglutinin or neuraminidase protein induced IFIT1 expression. Results showed that both H9N2 virus infection and viral particle inoculation induced the expression of IFIT1 at mRNA and protein levels in the two cell lines. Hemagglutinin or neuraminidase protein binding alone is not sufficient to induce IFIT1 expression. Surprisingly, the expression patterns of IFIT1 in response to H9N2 virus and viral particles in the two cell lines were opposite, and production kinetics of IFN-alpha/beta also differed. An additional finding was that induction of IFIT1 in response to H9N2 virus infection or viral particle inoculation was more sensitive in HUVECs than in BEAS-2Bs. Our data offers new insight into the innate immune response of endothelial cells to H9N2 virus infection.
引用
收藏
页码:271 / 281
页数:11
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