The IFITM Proteins Inhibit HIV-1 Infection

被引:340
作者
Lu, Jennifer [1 ,2 ]
Pan, Qinghua [1 ]
Rong, Liwei [1 ]
Liu, Shan-Lu [3 ,4 ]
Liang, Chen [1 ,2 ,3 ]
机构
[1] McGill Univ, Jewish Gen Hosp, McGill AIDS Ctr, Lady Davis Inst, Montreal, PQ H3T 1E2, Canada
[2] McGill Univ, Dept Med, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ H3A 2B4, Canada
[4] Univ Missouri, Dept Mol Microbiol & Immunol, Bond Life Sci Ctr, Columbia, MO 65211 USA
基金
加拿大健康研究院;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; STABLE SIGNAL PEPTIDE; WEST NILE VIRUS; INTERFERON-ALPHA; T-CELLS; IFN-ALPHA; ENVELOPE GLYCOPROTEIN; DISTINCT MECHANISMS; REPLICATION INVITRO; ANTIVIRAL RESPONSE;
D O I
10.1128/JVI.01531-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Type I interferon protects cells from virus infection through the induction of a group of genes collectively named interferon-stimulated genes (ISGs). In this study, we utilized short hairpin RNA (shRNA) to deplete ISGs in SupT1 cells in order to identify ISGs that suppress the production of human immunodeficiency virus type 1 (HIV-1). Among the ISG candidates thus identified were interferon-induced transmembrane (IFITM) proteins, including IFITM1, IFITM2, and IFITM3, that potently inhibit HIV-1 replication at least partially through interfering with virus entry. Further mutagenesis analysis shows that the intracellular region, rather than the N- and C-terminal extracellular domains, is essential for the antiviral activity of IFITM1. Altogether, these data suggest that the IFITM proteins serve as important components of the innate immune system to restrict HIV-1 infection.
引用
收藏
页码:2126 / 2137
页数:12
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