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乌昆耶米病毒出芽区室的免疫细胞化学分析:中间区室和高尔基体堆叠在病毒成熟中的作用

Immunocytochemical analysis of Uukuniemi virus budding compartments: role of the intermediate compartment and the Golgi stack in virus maturation.

作者信息

Jäntti J, Hildén P, Rönkä H, Mäkiranta V, Keränen S, Kuismanen E

机构信息

Department of Biosciences, University of Helsinki Biocenter, Finland.

出版信息

J Virol. 1997 Feb;71(2):1162-72. doi: 10.1128/JVI.71.2.1162-1172.1997.

Abstract

Previous studies have suggested that Uukuniemi virus, a bunyavirus, matures at the membranes of the Golgi complex. In this study we have employed immunocytochemical techniques to analyze in detail the budding compartment(s) of the virus. Electron microscopy of infected BHK-21 cells showed that virus particles are found in the cisternae throughout the Golgi stack. Within the cisternae, the virus particles were located preferentially in the dilated rims. This would suggest that virus budding may begin at or before the cis Golgi membranes. The virus budding compartment was studied further by immunoelectron microscopy with a pre-Golgi intermediate compartment marker, p58, and a Golgi stack marker protein, mannosidase II (ManII). Virus particles and budding virus were detected in ManII-positive Golgi stack membranes and, interestingly, in both juxtanuclear and peripheral p58-positive elements of the intermediate compartment. In cells incubated at 15 degrees C the nucleocapsid and virus envelope proteins were seen to accumulate in the intermediate compartment. Immunoelectron microscopy demonstrated that at 15 degrees C the nucleocapsid is associated with membranes that show a characteristic distribution and tubulo-vesicular morphology of the pre-Golgi intermediate compartment. These membranes contained virus particles in the lumen. The results indicate that the first site of formation of Uukuniemi virus particles is the pre-Golgi intermediate compartment and that virus budding continues in the Golgi stack. The results raise questions about the intracellular transport pathway of the virus particles, which are 100 to 120 nm in diameter and are therefore too large to be transported in the 60-nm-diameter vesicles postulated to function in the intra-Golgi transport. The distribution of the virus in the Golgi stack may imply that the cisternae themselves have a role in the vectorial transport of virus particles.

摘要

先前的研究表明,乌昆耶米病毒(一种布尼亚病毒)在高尔基体复合体的膜上成熟。在本研究中,我们采用免疫细胞化学技术详细分析了该病毒的出芽区室。对感染的BHK - 21细胞进行电子显微镜观察显示,在整个高尔基体堆栈的潴泡中都发现了病毒颗粒。在潴泡内,病毒颗粒优先位于扩张的边缘。这表明病毒出芽可能在顺面高尔基体膜处或之前就已开始。我们使用高尔基体前中间区室标志物p58和高尔基体堆栈标志物蛋白甘露糖苷酶II(ManII),通过免疫电子显微镜对病毒出芽区室进行了进一步研究。在ManII阳性的高尔基体堆栈膜中,有趣的是,在中间区室的近核和周边p58阳性成分中均检测到了病毒颗粒和出芽病毒。在15℃孵育的细胞中,核衣壳和病毒包膜蛋白积聚在中间区室。免疫电子显微镜显示,在15℃时,核衣壳与呈现高尔基体前中间区室特征性分布和管状 - 囊泡形态的膜相关联。这些膜的管腔内含有病毒颗粒。结果表明,乌昆耶米病毒颗粒形成的第一个位点是高尔基体前中间区室,并且病毒出芽在高尔基体堆栈中持续进行。这些结果引发了关于病毒颗粒细胞内运输途径的问题,该病毒颗粒直径为100至120 nm,因此太大而无法在假定参与高尔基体内运输的直径60 nm的囊泡中运输。病毒在高尔基体堆栈中的分布可能意味着潴泡本身在病毒颗粒的定向运输中发挥作用。

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