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一种诱导CD46早期主要下调的野生型日本麻疹病毒株。

A wild-type Japanese measles virus strain inducing predominant early down-regulation of CD46.

作者信息

Sakata H, Kurita M, Murakami Y, Nagasawa S, Watanabe M, Ueda S, Matsumoto M, Sato T, Kobune F, Seya T

机构信息

Department of Virus Disease and Vaccine Control, National Institute of Infectious Diseases, Musashimurayama, Tokyo, Japan.

出版信息

Biol Pharm Bull. 1998 Nov;21(11):1121-7. doi: 10.1248/bpb.21.1121.

DOI:10.1248/bpb.21.1121
PMID:9853398
Abstract

Down-regulation of CD46 secondary to stimulation with measles virus (MV) was investigated using CD46-positive cell lines and Japanese wild-type MV strains. The cells used were simian cell lines B95a and Vero in which MV strains have been adapted to be amplified, and Chinese hamster ovary (CHO) cell transfectants expressing human CD46 with (CHO(tail+)) or without (CHO(tail-)) the cytoplasmic tail. Of four Vero-adapted and three B95a-adapted MV strains, one Vero-adapted strain named Khono (KO), down-regulated CD46 within 60 min (early down-regulation) in all cell lines examined except Vero. No strains other than Toyoshima (TY), which induced early down-regulation only in CHO(tail+) cells, induced early down-regulation of CD46 in any combination. On the other hand, conventional down-regulation of CD46 was observed 24 h post-MV inoculation (late down-regulation) when cell lines used were adapted to MV strains. Thus, we concluded that there are two modes of CD46 down-regulation by MV and the unique strain KO markedly induces early down-regulation. Also, the CD46 homologue of B95a, which fails to act as a MV receptor, is down-regulated concomitantly with MV replication (>24 h) in cells principally by competent virus strains.

摘要

利用CD46阳性细胞系和日本野生型麻疹病毒(MV)株,研究了MV刺激后CD46的下调情况。所使用的细胞为已适应于扩增MV株的猿猴细胞系B95a和Vero,以及表达人CD46且带有(CHO(tail+))或不带有(CHO(tail-))细胞质尾的中国仓鼠卵巢(CHO)细胞转染体。在4株适应于Vero的MV株和3株适应于B95a的MV株中,1株名为Khono(KO)的适应于Vero的毒株,在60分钟内(早期下调)使除Vero外的所有检测细胞系中的CD46下调。除仅在CHO(tail+)细胞中诱导早期下调的丰岛(TY)外,没有其他毒株能以任何组合诱导CD46的早期下调。另一方面,当所用细胞系适应于MV株时,在接种MV后24小时观察到CD46的常规下调(晚期下调)。因此,我们得出结论,MV对CD46的下调有两种模式,独特的KO毒株显著诱导早期下调。此外,不能作为MV受体的B95a的CD46同源物,在细胞中主要由有活性的病毒株在MV复制(>24小时)时伴随下调。

相似文献

1
A wild-type Japanese measles virus strain inducing predominant early down-regulation of CD46.一种诱导CD46早期主要下调的野生型日本麻疹病毒株。
Biol Pharm Bull. 1998 Nov;21(11):1121-7. doi: 10.1248/bpb.21.1121.
2
Molecular cloning of membrane cofactor protein (MCP; CD46) on B95a cell, an Epstein-Barr virus-transformed marmoset B cell line: B95a-MCP is susceptible to infection by the CAM, but not the Nagahata strain of the measles virus.爱泼斯坦-巴尔病毒转化的狨猴B细胞系B95a细胞上膜辅因子蛋白(MCP;CD46)的分子克隆:B95a-MCP对CAM株敏感,但对麻疹病毒长畑株不敏感。
Biochem J. 1998 Mar 15;330 ( Pt 3)(Pt 3):1351-9. doi: 10.1042/bj3301351.
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Effect of mutations at the residues R25, D27, P69, and N70 of B95a-MCP on receptor activities for the measles viruses Nagahata wild-type strain and CAM vaccine strain.
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Multiple isoforms of CD46 (membrane cofactor protein) serve as receptors for measles virus.CD46(膜辅因子蛋白)的多种亚型可作为麻疹病毒的受体。
Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2161-5. doi: 10.1073/pnas.91.6.2161.
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Functional modulation of human macrophages through CD46 (measles virus receptor): production of IL-12 p40 and nitric oxide in association with recruitment of protein-tyrosine phosphatase SHP-1 to CD46.通过CD46(麻疹病毒受体)对人巨噬细胞进行功能调节:白细胞介素-12 p40和一氧化氮的产生与蛋白酪氨酸磷酸酶SHP-1募集到CD46相关。
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Receptor usage and differential downregulation of CD46 by measles virus wild-type and vaccine strains.麻疹病毒野生型和疫苗株对CD46的受体利用及差异性下调
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Adaptation of wild-type measles virus to CD46 receptor usage.野生型麻疹病毒对CD46受体利用的适应性
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Efficiency of measles virus entry and dissemination through different receptors.麻疹病毒通过不同受体进入和传播的效率。
J Virol. 2002 Aug;76(15):7460-7. doi: 10.1128/jvi.76.15.7460-7467.2002.
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Differential receptor usage by measles virus strains.麻疹病毒株的受体使用差异
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The CD46 transmembrane domain is required for efficient formation of measles-virus-mediated syncytium.麻疹病毒介导的合胞体高效形成需要CD46跨膜结构域。
Biochem J. 1997 Feb 15;322 ( Pt 1)(Pt 1):135-44. doi: 10.1042/bj3220135.

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