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感染昆金黄病毒的非洲绿猴肾细胞中的免疫荧光位点。

Immunofluorescent sites in vero cells infected with the flavivirus Kunjin.

作者信息

Ng M L, Pedersen J S, Toh B H, Westaway E G

出版信息

Arch Virol. 1983;78(3-4):177-90. doi: 10.1007/BF01311313.

Abstract

The sites of replication and of accumulation of viral macromolecules were examined using fluorescent antibodies to viral products and to cell organelles. Synthesis of envelope protein and its accumulation in a narrow rim around the nucleus were detected at 4 hours post infection; concurrently, a progressive change was observed in the rough endoplasmic reticulum from a fine to a coarse network emanating from around the nucleus. This change in the network was visible by light microscopy. The immunofluorescent sites of viral RNA synthesis, located by use of anti-double stranded RNA, extended from the perinuclear region in another fine network which included many small foci or vesicles; these sites were also visible by light microscopy late in infection. None of these changes were associated with any visible redistribution of actin, intermediate filaments or microtubules, and no nuclear involvement was detected. However, when microtubules were disrupted by vinblastine treatment of cells, the distribution of the immunofluorescent sites of viral RNA synthesis was modified and the virus yield was reduced by at least 10-fold. These results confirmed our biochemical studies showing separation of viral sites of RNA synthesis and translation, and the accumulation of envelope protein in nuclear-associated membranes. The relevance of these observations is discussed in relation to the reports of specific membrane structures induced in flavivirus-infected cells.

摘要

利用针对病毒产物和细胞器的荧光抗体,对病毒大分子的复制和积累位点进行了检测。感染后4小时检测到包膜蛋白的合成及其在细胞核周围窄边缘的积累;同时,观察到粗面内质网从细胞核周围发出的精细网络逐渐变为粗糙网络。这种网络变化在光学显微镜下可见。利用抗双链RNA定位的病毒RNA合成的免疫荧光位点,从核周区域延伸至另一个精细网络,该网络包含许多小焦点或小泡;在感染后期,这些位点在光学显微镜下也可见。这些变化均与肌动蛋白、中间丝或微管的任何可见重新分布无关,且未检测到细胞核受累。然而,当用长春花碱处理细胞破坏微管时,病毒RNA合成的免疫荧光位点分布发生改变,病毒产量至少降低10倍。这些结果证实了我们的生化研究,即病毒RNA合成和翻译位点的分离,以及包膜蛋白在核相关膜中的积累。结合黄病毒感染细胞中诱导的特定膜结构的报道,对这些观察结果的相关性进行了讨论。

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