The mucosal expression pattern of interferon-ε in rhesus macaques

被引:35
作者
Demers, Andrew [1 ]
Kang, Guobin [1 ]
Ma, Fungrui [1 ]
Lu, Wuxun [1 ]
Yuan, Zhe [1 ]
Li, Yue [1 ,2 ]
Lewis, Mark [3 ]
Kraiselburd, Edmundo N. [4 ]
Montaner, Luis [5 ]
Li, Qingsheng [1 ]
机构
[1] Univ Nebraska, Sch Biol Sci, Nebraska Ctr Virol, Lincoln, NE 68583 USA
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
[3] Bioqual, Rockville, MD USA
[4] Univ Puerto Rico, Sch Med, Dept Microbiol & Zool, San Juan, PR 00936 USA
[5] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Simian Immunodeficiency Virus; SIV; type I interferons; IFN-I; mucosal immunity; MULTIPLE SEQUENCE ALIGNMENT; I INTERFERON; MICROARRAY ANALYSIS; GENE-EXPRESSION; INDUCTION; MUSCLE; VIRUS; CELLS; BETA;
D O I
10.1189/jlb.3A0214-088RRR
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The expression of INF-epsilon in multiple mucosal tissues of rhesus macaques. Type I IFNs play an important role in innate and adaptive immunity against viral infections. A novel type I IFN, namely IFN-epsilon, which can protect against vaginal transmission of HSV2 and Chlamydia muridarum bacterial infection, has been described in mice and humans. Nevertheless, the principle cell type and the expression pattern of IFN-epsilon in tissues remain uncertain. In addition, the expression of IFN-epsilon in Indian rhesus macaques (Macaca mulatta) has not been reported. Here, we analyzed IFN-epsilon expression in multiple mucosal sites of uninfected or SIV-infected Indian rhesus macaques using IHCS. We report for the first time the detection of IFN-epsilon expression in situ in the lung, foreskin, vaginal, cervical, and small and large intestinal mucosae of rhesus macaques. We found that the expression of IFN-epsilon was exclusive to the epithelial cells in all of the aforementioned mucosal tissues. Furthermore, the macaque IFN-epsilon sequence in this study revealed that macaque IFN-epsilon is highly conserved among human and other nonhuman primates. Lastly, SIV rectal infection did not significantly alter the expression of IFN-epsilon in rectal mucosae. Together, these findings indicate that IFN-epsilon may function as the first line of defense against the invasion of mucosal pathogens. Further studies should be conducted to examine IFN-epsilon protection against gastrointestinal as well as respiratory infections.
引用
收藏
页码:1101 / 1107
页数:7
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