Department of Pathology, Xi Jing Hospital, Fourth Military Medical University Xi'an, Shaanxi 710032, China.
Am J Transl Res. 2009 Jul 15;1(4):367-80.
Hantavirus (HTV) infection is known to induce innate cellular response, a more specified cellular response in the host cells. However, whether it stimulates synthesis of stress proteins, particularly associations of viral proteins, is entirely unknown. The primary focus of this research is using Vero E6 cells infected with Hantaan 76-118 (HTNV) as an in vitro infection model to examine the individual contribution of HTV infection to heat shock response. This study shows that HTNV infection rapidly induced HSP70 expression in Vero E6 cells, which underwent a nucleo-cytoplasmic shuttle that lasted for more than 3 d. The increased HSP70 was preceded by induction of HSP70 mRNA. The physical association of HSP70 with viral nucleocapsid protein (NP) in infected cells was demonstrated by co-localization and immunoprecipation. Vero E6 cells that constitutively overexpress HSP70 after stable transfection with HSP70 gene, when infected with HTNV, showed selectively reduced NP synthesis. These findings suggest HSP70 is actively involved in the control of the expression level of viral structural proteins and possibly involved in virus assembly by binding of NP to HSP70. Overexpression of HSP70 does not favor viral propagation.
汉坦病毒(HTV)感染已知会诱导先天细胞反应,即宿主细胞中更特异的细胞反应。然而,它是否刺激应激蛋白的合成,特别是病毒蛋白的关联,目前还完全不清楚。本研究的主要重点是使用感染汉坦病毒 76-118(HTNV)的 Vero E6 细胞作为体外感染模型,来检测 HTV 感染对热休克反应的个体贡献。本研究表明,HTNV 感染迅速诱导 Vero E6 细胞中 HSP70 的表达,该表达经历了超过 3 天的核质穿梭。HSP70 mRNA 的诱导先于 HSP70 的增加。通过共定位和免疫沉淀,证明 HSP70 与感染细胞中的病毒核衣壳蛋白(NP)的物理关联。通过 HSP70 基因的稳定转染,在用 HTNV 感染后,持续过表达 HSP70 的 Vero E6 细胞表现出 NP 合成的选择性减少。这些发现表明 HSP70 积极参与控制病毒结构蛋白的表达水平,并可能通过与 HSP70 的结合参与病毒组装。HSP70 的过表达不利于病毒的繁殖。