Kamata M, Hiraki A, Kim J
Institute of Molecular and Cellular Biology for Pharmaceutical Sciences, Kyoto Pharmaceutical University, Japan.
Cell Struct Funct. 1994 Oct;19(5):315-23. doi: 10.1247/csf.19.315.
Production of HVJ (Sendai virus) virion is suppressed in the infected LLC-MK2 cells in the low Ca2+ condition. To clarify this phenomenon, the effect of Ca2+ on HVJ morphogenesis was examined under normal and low Ca2+ conditions. The HVJ production was observed in standard medium (containing 1.8 mM Ca2+) within 24 hr after infection and increased with the culture time. Indirect immunofluorescent staining with an anti-HVJ envelope antibody showed that the viral glycoproteins, HANA (HN) and F proteins, were synthesized within 10 hr after infection, diffused to the cell surface, and then many patches strongly stained with this antibody were formed on the cell surface. In contrast, when the infected cells were cultured in low Ca2+ medium, viral glycoproteins were synthesized as in the case of standard medium. However, the glycoproteins were almost all accumulated in the Golgi apparatus, suggesting that expression of viral glycoproteins at the cell surface was suppressed, and the patches were hardly seen on the cell surface. When the low Ca2+ medium was replaced by standard medium, the accumulated viral glycoproteins were rapidly diffused and expressed on the cell surface, HVJ production was restored and patches formed on the cell surface. By confocal laser scanning microscopy, the results were seen more clearly; Ca2+ is necessary for the expression of viral glycoproteins at the cell surface. By electron microscopy under normal conditions, groups of viral budding sites were seen collected in restricted areas, corresponding to the patches observed on immunofluorescent staining, but the budding sites were not seen on the cells cultured in low Ca2+ medium.(ABSTRACT TRUNCATED AT 250 WORDS)
在低钙条件下,感染的LLC - MK2细胞中HVJ(仙台病毒)病毒粒子的产生受到抑制。为阐明这一现象,研究了正常和低钙条件下钙对HVJ形态发生的影响。感染后24小时内在标准培养基(含1.8 mM钙)中观察到HVJ产生,并随培养时间增加。用抗HVJ包膜抗体进行间接免疫荧光染色显示,病毒糖蛋白HANA(HN)和F蛋白在感染后10小时内合成,扩散到细胞表面,然后细胞表面形成许多被该抗体强烈染色的斑块。相比之下,当感染细胞在低钙培养基中培养时,病毒糖蛋白的合成与在标准培养基中情况相同。然而,糖蛋白几乎都聚集在高尔基体中,这表明细胞表面病毒糖蛋白的表达受到抑制,细胞表面几乎看不到斑块。当将低钙培养基换成标准培养基时,积累的病毒糖蛋白迅速扩散并在细胞表面表达,HVJ产生恢复,细胞表面形成斑块。通过共聚焦激光扫描显微镜观察,结果更清晰;钙对于病毒糖蛋白在细胞表面的表达是必需的。在正常条件下通过电子显微镜观察,病毒出芽位点聚集在特定区域,与免疫荧光染色中观察到的斑块相对应,但在低钙培养基中培养的细胞上未观察到出芽位点。(摘要截短至250字)