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宿主细胞中 ATP 的生成增加是有效生产牛痘病毒所必需的。

Increased ATP generation in the host cell is required for efficient vaccinia virus production.

机构信息

Graduate Institute of Molecular and Cellular Biology, Tzu Chi University, Hualien, Taiwan, Republic of China.

出版信息

J Biomed Sci. 2009 Sep 2;16(1):80. doi: 10.1186/1423-0127-16-80.

Abstract

To search for cellular genes up-regulated by vaccinia virus (VV) infection, differential display-reverse transcription-polymerase chain reaction (ddRT-PCR) assays were used to examine the expression of mRNAs from mock-infected and VV-infected HeLa cells. Two mitochondrial genes for proteins that are part of the electron transport chain that generates ATP, ND4 and CO II, were up-regulated after VV infection. Up-regulation of ND4 level by VV infection was confirmed by Western blotting analysis. Up-regulation of ND4 was reduced by the MAPK inhibitor, apigenin, which has been demonstrated elsewhere to inhibit VV replication. The induction of ND4 expression occurred after viral DNA replication since ara C, an inhibitor of poxviral DNA replication, could block this induction. ATP production was increased in the host cells after VV infection. Moreover, 4.5 microM oligomycin, an inhibitor of ATP production, reduced the ATP level 13 hr after virus infection to that of mock-infected cells and inhibited viral protein expression and virus production, suggesting that increased ATP production is required for efficient VV production. Our results further suggest that induction of ND4 expression is through a Bcl-2 independent pathway.

摘要

为了寻找被痘苗病毒(VV)感染上调的细胞基因,我们使用差异显示反转录聚合酶链反应(ddRT-PCR)试验来检测mock 感染和 VV 感染的 HeLa 细胞中 mRNA 的表达。在 VV 感染后,两个线粒体基因(编码电子传递链中生成 ATP 的蛋白质的一部分)ND4 和 CO II 的表达水平上调。Western 印迹分析证实了 VV 感染对 ND4 水平的上调。MAPK 抑制剂芹菜素(apigenin)抑制了 VV 的复制,从而降低了 ND4 的上调。ND4 的诱导发生在病毒 DNA 复制之后,因为 ara C(一种抑制痘病毒 DNA 复制的抑制剂)可以阻断这种诱导。在 VV 感染后,宿主细胞中的 ATP 产量增加。此外,4.5μM 的寡霉素(一种抑制 ATP 产生的抑制剂)将病毒感染 13 小时后的 ATP 水平降低到 mock 感染细胞的水平,并抑制病毒蛋白表达和病毒产生,表明增加的 ATP 产生对于有效的 VV 产生是必需的。我们的结果进一步表明,ND4 表达的诱导是通过 Bcl-2 非依赖性途径实现的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccbd/2741444/0ee6f2a805d4/1423-0127-16-80-1.jpg

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