Enhancement of phospholipase D activity following baculovirus and adenovirus infection in Sf9 and COS-7 cells

Ariane Höer, Torsten Schöneberg, Christian Harteneck, Cigdem Cetindag, Eckard Oberdisse
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引用次数: 2

Abstract

In order to purify the human phospholipase D1 (hPLD1) for analysis of its functional properties, we applied a baculovirus-based high-expression system. As expected, Sf9 cells infected with a baculovirus encoding for the hPLD1 displayed a 7.5-fold increase in PLD activity compared to uninfected cells. Sf9 cells infected with the wild-type (WT) and other recombinant baculoviruses were used as an expression control. Surprisingly, all baculoviruses tested led to a 3–5-fold increase in basal PLD activity when compared to uninfected cells. To further characterize the nature of the increased PLD activity, the influence of ADP-ribosylation factor (ARF) and phorbol 12-myristate 13-acetate (PMA) was studied. In contrast to membranes containing the hPLD1, the PLD activity in membranes from uninfected and WT-infected Sf9 cells was not stimulated by ARF. PMA did not affect the increase in PLD activity in any case. To further study whether the virus-mediated increase in PLD activity is a more general phenomenon, we infected COS-7 cells with recombinant and WT adenoviruses. Only the infection with the WT adenovirus resulted in an approx. 2-fold increase in PLD activity. Our results demonstrate for the first time that a viral infection elevates the PLD activity in insect and mammalian cells.

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杆状病毒和腺病毒感染Sf9和COS-7细胞后磷脂酶D活性的增强
为了纯化人磷脂酶D1 (hPLD1)并分析其功能特性,我们采用了基于杆状病毒的高表达系统。正如预期的那样,被编码hPLD1的杆状病毒感染的Sf9细胞与未感染的细胞相比,PLD活性增加了7.5倍。用野生型(WT)和其他重组杆状病毒感染的Sf9细胞作为表达对照。令人惊讶的是,与未感染的细胞相比,所有杆状病毒测试导致基础PLD活性增加3 - 5倍。为了进一步表征PLD活性增加的性质,我们研究了adp -核糖基化因子(ARF)和phorbol 12-肉豆酸酯13-乙酸酯(PMA)的影响。与含有hPLD1的膜相比,未感染和wt感染的Sf9细胞膜中的PLD活性未被ARF刺激。在任何情况下,PMA都不影响PLD活性的增加。为了进一步研究病毒介导的PLD活性升高是否是一种更普遍的现象,我们用重组腺病毒和WT腺病毒感染COS-7细胞。只有WT腺病毒的感染导致了大约。PLD活性增加2倍。我们的研究结果首次证明了病毒感染可提高昆虫和哺乳动物细胞中PLD的活性。
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