Exosomes in human semen restrict HIV-1 transmission by vaginal cells and block intravaginal replication of LP-BM5 murine AIDS virus complex

被引:92
作者
Madison, Marisa N. [1 ]
Jones, Philip H. [1 ]
Okeoma, Chioma M. [1 ,2 ]
机构
[1] Univ Iowa, Dept Microbiol, Carver Coll Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Interdisciplinary Program Mol & Cellular Biol, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
Exosome; Semen; Vaginal epithelia; HIV; Murine AIDS; mAIDS; LP-BM5; virus; HUMAN-IMMUNODEFICIENCY-VIRUS; FEMALE GENITAL-TRACT; PLASMA VIRAL LOAD; CD4(+) T-CELLS; SEXUAL TRANSMISSION; EPITHELIAL-CELLS; HETEROSEXUAL TRANSMISSION; IN-VIVO; ADAPTIVE IMMUNITY; LANGERHANS CELLS;
D O I
10.1016/j.virol.2015.03.040
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Exosomes are membranous extracellular nanovesicles secreted by diverse cell types. Exosomes from healthy human semen have been shown to inhibit HIV-1 replication and to impair progeny virus infectivity. In this study, we examined the ability of healthy human semen exosomes to restrict HIV-1 and LP-BM5 murine AIDS virus transmission in three different model systems. We show that vaginal cells internalize exosomes with concomitant transfer of functional mRNA. Semen exosomes blocked the spread of HIV-1 from vaginal epithelial cells to target cells in our cell-to-cell infection model and suppressed transmission of HIV-1 across the vaginal epithelial barrier in our trans-well model. Our in vivo model shows that human semen exosomes restrict intravaginal transmission and propagation of murine AIDS virus. Our study highlights an antiretroviral role for semen exosomes that may be harnessed for the development of novel therapeutic strategies to combat HIV-1 transmission. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 201
页数:13
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