Tashiro M, McQueen N L, Seto J T, Klenk H D, Rott R
Department of Virology 1, National Institute of Health, Tokyo, Japan.
J Virol. 1996 Sep;70(9):5990-7. doi: 10.1128/JVI.70.9.5990-5997.1996.
Wild-type Sendai virus buds at the apical plasma membrane domain of polarized epithelial MDCK cells, whereas a pantropic mutant, F1-R, buds at both the apical and basolateral domains. In F1-R-infected cells, polarized protein transport and the microtubule network are impaired. It has been suggested that the mutated F and/or M proteins in F1-R are responsible for these changes (M. Tashiro, J. T. Seto, H.-D. Klenk, and R. Rott, J. Virol. 67:5902-5910, 1993). To clarify which gene or mutation(s) was responsible for the microtubule disruption which leads to altered budding of F1-R, MDCK cell lines containing the M gene of either the wild type or F1-R were established. When wild-type M protein was expressed at a level corresponding to that synthesized in virus-infected cells, cellular polarity and the integrity of the microtubules were affected to some extent. On the other hand, expression of the mutated F1-R M protein resulted in the formation of giant cells about 40 times larger than normal MDCK cells. Under these conditions, the effects on the microtubule network were enhanced. The microtubules were disrupted and polarized protein transport was impaired as indicated by the nonpolarized secretion of gp80, a host cell glycoprotein normally secreted from the apical domain, and bipolar budding of wild-type and F1-R Sendai viruses. The mutated F glycoprotein of F1-R was transported bipolarly in cells expressing the F1-R M protein, whereas it was transported predominantly to the apical domain when expressed alone or in cells coexpressing the wild-type M protein. These findings indicate that the M protein of F1-R is involved in the disruption of the microtubular network, leading to impairment of cellular polarity, bipolar transport of the F glycoprotein, and bipolar budding of the virus.
野生型仙台病毒在极化上皮MDCK细胞的顶端质膜结构域出芽,而泛嗜性突变体F1-R在顶端和基底外侧结构域均出芽。在感染F1-R的细胞中,极化蛋白转运和微管网络受损。有人提出F1-R中突变的F和/或M蛋白是这些变化的原因(M. 田代、J. T. 濑户、H.-D. 克伦克和R. 罗特,《病毒学杂志》67:5902-5910,1993年)。为了阐明是哪个基因或哪些突变导致了微管破坏从而致使F1-R出芽改变,建立了含有野生型或F1-R的M基因的MDCK细胞系。当野生型M蛋白以与病毒感染细胞中合成水平相当的水平表达时,细胞极性和微管的完整性在一定程度上受到影响。另一方面,突变的F1-R M蛋白的表达导致形成比正常MDCK细胞大40倍左右的巨细胞。在这些条件下,对微管网络的影响增强。微管被破坏,极化蛋白转运受损,这表现为宿主细胞糖蛋白gp80(通常从顶端结构域分泌)的非极化分泌以及野生型和F1-R仙台病毒的双极出芽。F1-R的突变F糖蛋白在表达F1-R M蛋白的细胞中双极转运,而当单独表达或在共表达野生型M蛋白的细胞中表达时,它主要转运到顶端结构域。这些发现表明F1-R的M蛋白参与了微管网络的破坏,导致细胞极性受损、F糖蛋白的双极转运以及病毒的双极出芽。