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I型和III型干扰素都是限制麻疹病毒在肺上皮细胞中生长所必需的。

Both type I and type III interferons are required to restrict measles virus growth in lung epithelial cells.

作者信息

Taniguchi Midori, Yanagi Yusuke, Ohno Shinji

机构信息

Department of Virology, Faculty of Medicine, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Department of Virology, Graduate School of Medicine, University of the Ryukyus, 207 Uehara, Nishihara, Nakagami, Okinawa, 903-0215, Japan.

出版信息

Arch Virol. 2019 Feb;164(2):439-446. doi: 10.1007/s00705-018-4087-0. Epub 2018 Nov 2.

Abstract

Measles virus (MeV) first infects immune cells in the respiratory tract of a human host, spreads to lymphoid organs throughout the body, and finally enters and grows in respiratory epithelial cells before being released and transmitted to the next host. Thus, efficient growth in respiratory epithelial cells is important for the person-to-person transmission of MeV. Upon viral entry, host cells detect viral nucleic acids and produce interferons (IFNs) to control viral growth. Type I (IFN-α/β) and type III (IFN-λ) IFNs have largely common induction and signaling mechanisms and stimulate expression of similar target genes but utilize distinct receptors. To determine the relative contributions of type I and type III IFNs to the control of MeV growth in epithelial cells, we examined the growth of MeV and that of its mutants lacking either type I or type III IFN receptor in the human lung epithelial cell line H358. Our results revealed that both type I and type III IFNs are required to restrict MeV growth in H358 cells and that the induction of type III as well as type I IFNs was increased in the absence of the MeV nonstructural V protein.

摘要

麻疹病毒(MeV)首先感染人类宿主呼吸道中的免疫细胞,扩散至全身的淋巴器官,最终进入呼吸道上皮细胞并在其中生长,然后被释放并传播给下一个宿主。因此,在呼吸道上皮细胞中高效生长对于MeV的人际传播很重要。病毒进入后,宿主细胞检测病毒核酸并产生干扰素(IFN)以控制病毒生长。I型(IFN-α/β)和III型(IFN-λ)干扰素在很大程度上具有共同的诱导和信号传导机制,并刺激相似靶基因的表达,但利用不同的受体。为了确定I型和III型干扰素对控制上皮细胞中MeV生长的相对贡献,我们检测了MeV及其缺乏I型或III型干扰素受体的突变体在人肺上皮细胞系H358中的生长情况。我们的结果显示,I型和III型干扰素都是限制H358细胞中MeV生长所必需的,并且在没有MeV非结构V蛋白的情况下,III型以及I型干扰素的诱导均增加。

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