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麻疹病毒在上皮细胞中的进入和释放具有极性。

Entry and release of measles virus are polarized in epithelial cells.

作者信息

Blau D M, Compans R W

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Rollins Research Center, Atlanta, Georgia 30322, USA.

出版信息

Virology. 1995 Jun 20;210(1):91-9. doi: 10.1006/viro.1995.1320.

Abstract

The initial site of virus replication during measles infection is in the epithelial cells of the respiratory tract. We have investigated measles virus infection of two types of polarized epithelial cells to determine if entry and/or release of the virus is confined to either the apical or the basolateral plasma membrane. The Caco-2 line of human intestinal epithelial cells and the polarized Vero C1008 monkey kidney cell line were grown on permeable supports and inoculated either through the apical or basolateral surfaces. Cells exposed to virus in the apical medium showed high levels of synthesis of virus-specific proteins, whereas no synthesis of viral proteins was detected in cells inoculated at the basolateral surface. Virus titers derived from apically infected cells were found to be about 1000-fold greater than titers derived from cells infected at the basolateral surface. Indirect immunofluorescence results also demonstrated that expression of measles viral antigens occurs at high levels only when input virions are inoculated at the apical surface. To investigate the localization of CD46 and moesin, which are receptors for measles virus, Caco-2 cells were incubated with monoclonal antibodies against CD46 or moesin followed by 125I-labeled anti-mouse Ig. The results indicate that CD46 is expressed preferentially on the apical membranes while moesin appears to be present at similar levels on both surfaces. Release of the virus was also examined and found to be polarized as well. Virus was released into the apical medium at up to 1000-fold higher titers than virus released into the basolateral medium. These results demonstrate that in two epithelial cell types measles virus preferentially enters and is released from epithelial cells in a polarized fashion through the apical plasma membrane.

摘要

麻疹感染期间病毒复制的初始部位是呼吸道上皮细胞。我们研究了麻疹病毒对两种极化上皮细胞的感染情况,以确定病毒的进入和/或释放是否局限于顶端或基底外侧质膜。人肠道上皮细胞系Caco-2和极化的Vero C1008猴肾细胞系在可渗透支持物上生长,并通过顶端或基底外侧表面接种。暴露于顶端培养基中病毒的细胞显示出高水平的病毒特异性蛋白合成,而在基底外侧表面接种的细胞中未检测到病毒蛋白的合成。发现源自顶端感染细胞的病毒滴度比源自基底外侧感染细胞的滴度高约1000倍。间接免疫荧光结果也表明,仅当输入病毒体接种在顶端表面时,麻疹病毒抗原才会高水平表达。为了研究麻疹病毒受体CD46和埃兹蛋白的定位,将Caco-2细胞与抗CD46或埃兹蛋白的单克隆抗体孵育,然后用125I标记的抗小鼠Ig进行检测。结果表明,CD46优先在顶端膜上表达,而埃兹蛋白在两个表面的表达水平相似。还对病毒的释放进行了检测,发现其也是极化的。释放到顶端培养基中的病毒滴度比释放到基底外侧培养基中的病毒滴度高多达1000倍。这些结果表明,在两种上皮细胞类型中,麻疹病毒优先以极化方式通过顶端质膜进入上皮细胞并从上皮细胞中释放。

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