کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5917022 | 1163768 | 2014 | 11 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
MAVS-dependent IRF3/7 bypass of interferon β-induction restricts the response to measles infection in CD150Tg mouse bone marrow-derived dendritic cells
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کلمات کلیدی
RIG-IMDA5MAVSmelanoma differentiation associated gene 5retinoic acid inducible gene-IInnate immunity - ایمنی ذاتیType I interferon - اینترفرون نوع IDendritic cells - سلول های دندریتیکbone marrow - مغز استخوانwild-type - نوع وحشیMeasles virus - ویروس سرخکmitochondrial antiviral signaling protein - پروتئین سیگنالینگ ضد ویروسی میتوکندری
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شناسی مولکولی
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چکیده انگلیسی
Measles virus (MV) infects CD150Tg/Ifnar (IFN alpha receptor)â/â mice but not CD150 (a human MV receptor)-transgenic (Tg) mice. We have shown that bone marrow-derived dendritic cells (BMDCs) from CD150Tg/Ifnarâ/â mice are permissive to MV in contrast to those from simple CD150Tg mice, which reveals a crucial role of type I interferon (IFN) in natural tropism against MV. Yet, the mechanism whereby BMDCs produce initial type I IFN has not been elucidated in MV infection. RNA virus infection usually allows cells to generate double-stranded RNA and induce activation of IFN regulatory factor (IRF) 3/7 transcription factors, leading to the production of type I IFN through the retinoic acid-inducible gene I (RIG-I)/melanoma differentiation-associated gene 5 (MDA5)-mitochondrial antiviral signaling protein (MAVS) pathway. In mouse experimental BMDCs models, we found CD150Tg/Mavsâ/âBMDCs, but not CD150Tg/Irf3â/â/Irf7â/âBMDCs, permissive to MV. IFN-α/β were not induced in MV-infected CD150Tg/Mavsâ/âBMDCs, while IFN-β was subtly induced in CD150Tg/Irf3â/â/Irf7â/âBMDCs. In vivo systemic infection was therefore established by transfer of MV-infected CD150Tg/Mavsâ/â BMDCs to CD150Tg/Ifnarâ/â mice. These data indicate that MAVS-dependent, IRF3/7-independent IFN-β induction triggers the activation of the IFNAR pathway so as to restrict the spread of MV by infected BMDCs. Hence, MAVS participates in the initial induction of type I IFN in BMDCs and IFNAR protects against MV spreading. We also showed the importance of IL-10-producing CD4+ T cells induced by MV-infected BMDCs in vitro, which may account for immune modulation due to the functional aberration of DCs.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Immunology - Volume 57, Issue 2, February 2014, Pages 100-110
Journal: Molecular Immunology - Volume 57, Issue 2, February 2014, Pages 100-110
نویسندگان
Hiromi Takaki, Kenya Honda, Koji Atarashi, Fukiko Kobayashi, Takashi Ebihara, Hiroyuki Oshiumi, Misako Matsumoto, Masashi Shingai, Tsukasa Seya,