TY - JOUR
T1 - The mucosal expression pattern of interferon-ε in Rhesus Macaques
AU - Demers, Andrew
AU - Kang, Guobin
AU - Ma, Fungrui
AU - Lu, Wuxun
AU - Yuan, Zhe
AU - Li, Yue
AU - Lewis, Mark
AU - Kraiselburd, Edmundo N.
AU - Montaner, Luis
AU - Li, Qingsheng
N1 - Publisher Copyright:
© Society for Leukocyte Biology.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Type I IFNs play an important role in innate and adaptive immunity against viral infections. A novel type I IFN, namely IFN-ε, 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-ε in tissues remain uncertain. In addition, the expression of IFN-ε in Indian rhesus macaques (Macaca mulatta) has not been reported. Here, we analyzed IFN-ε 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-ε 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-ε was exclusive to the epithelial cells in all of the aforementioned mucosal tissues. Furthermore, the macaque IFN-ε sequence in this study revealed that macaque IFN-ε is highly conserved among human and other nonhuman primates. Lastly, SIV rectal infection did not significantly alter the expression of IFN-ε in rectal mucosae. Together, these findings indicate that IFN-ε may function as the first line of defense against the invasion of mucosal pathogens. Further studies should be conducted to examine IFN-ε protection against gastrointestinal as well as respiratory infections.
AB - Type I IFNs play an important role in innate and adaptive immunity against viral infections. A novel type I IFN, namely IFN-ε, 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-ε in tissues remain uncertain. In addition, the expression of IFN-ε in Indian rhesus macaques (Macaca mulatta) has not been reported. Here, we analyzed IFN-ε 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-ε 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-ε was exclusive to the epithelial cells in all of the aforementioned mucosal tissues. Furthermore, the macaque IFN-ε sequence in this study revealed that macaque IFN-ε is highly conserved among human and other nonhuman primates. Lastly, SIV rectal infection did not significantly alter the expression of IFN-ε in rectal mucosae. Together, these findings indicate that IFN-ε may function as the first line of defense against the invasion of mucosal pathogens. Further studies should be conducted to examine IFN-ε protection against gastrointestinal as well as respiratory infections.
KW - IFN-I
KW - Mucosal immunity
KW - SIV
KW - Simian Immunodeficiency Virus
KW - Type I interferons
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U2 - 10.1189/jlb.3A0214-088RRR
DO - 10.1189/jlb.3A0214-088RRR
M3 - Article
C2 - 25139290
AN - SCOPUS:84914180819
SN - 0741-5400
VL - 96
SP - 1101
EP - 1107
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
IS - 6
ER -