Wang Wei, Ye Linbai, Ye Li, Li Baozong, Gao Bo, Zeng Yingchun, Kong Lingbao, Fang Xiaonan, Zheng Hong, Wu Zhenghui, She Yinglong
State Key Laboratory of Virology, College of Life Science, Wuhan University, Wuhan, Hubei 430072, China.
Virus Res. 2007 Sep;128(1-2):1-8. doi: 10.1016/j.virusres.2007.02.007. Epub 2007 May 25.
The clinical picture of severe acute respiratory syndrome (SARS) is characterized by an over-exuberant immune response with lung lymphomononuclear cells infilteration and proliferation that may account for tissue damage more than the direct effect of viral replication. To understand how cells response in the early stage of virus-host cell interaction, in this study, a purified recombinant S protein was studied for stimulating murine macrophages (RAW264.7) to produce proinflammatory cytokines (IL-6 and TNF-alpha) and chemokine IL-8. We found that direct induction of IL-6 and TNF-alpha release in the supernatant in a dose-, time-dependent manner and highly spike protein-specific, but no induction of IL-8 was detected. Further experiments showed that IL-6 and TNF-alpha production were dependent on NF-kappaB, which was activated through I-kappaBalpha degradation. These results suggest that SARS-CoV spike protein may play an important role in the pathogenesis of SARS, especially in inflammation and high fever.
严重急性呼吸综合征(SARS)的临床症状表现为免疫反应过度活跃,伴有肺淋巴单核细胞浸润和增殖,这可能比病毒复制的直接作用更能导致组织损伤。为了解细胞在病毒与宿主细胞相互作用早期的反应,在本研究中,对纯化的重组S蛋白进行了研究,以刺激小鼠巨噬细胞(RAW264.7)产生促炎细胞因子(IL-6和TNF-α)和趋化因子IL-8。我们发现,重组S蛋白能以上清液中IL-6和TNF-α的释放呈剂量和时间依赖性,且具有高度的刺突蛋白特异性,但未检测到对IL-8的诱导作用。进一步实验表明,IL-6和TNF-α的产生依赖于NF-κB,而NF-κB是通过I-κBα降解而被激活的。这些结果表明,SARS-CoV刺突蛋白可能在SARS的发病机制中起重要作用,尤其是在炎症和高热方面。