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首页> 外文期刊>Journal of Biotechnology >Transformed lepidopteran cells expressing a protein of the silkmoth fat body display enhanced susceptibility to baculovirus infection and produce high titers of budded virus in serum-free media
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Transformed lepidopteran cells expressing a protein of the silkmoth fat body display enhanced susceptibility to baculovirus infection and produce high titers of budded virus in serum-free media

机译:表达蚕蛾脂肪体蛋白质的转化鳞翅目细胞对杆状病毒感染的敏感性增强,并且在无血清培养基中产生高滴度的发芽病毒

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摘要

Baculovirus vectors constitute important tools for therapeutic protein production and mammalian cell transduction for gene therapy applications. A prerequisite for such applications is that the cell lines in which baculoviruses are propagated be maintained in serum-free media that are devoid of potential human pathogens. However, in serum-free media, the performance of baculovirus-based systems can be significantly reduced. In this report, we show that silkmoth-derived host cell lines for the Bombyx mori-nuclear polyhedrosis virus (BmNPV) that are transformed with the gene for the promoting protein (PP), a silkmoth-derived secreted factor containing a lipid-binding domain, display enhanced susceptibility to BmNPV infection and enhanced budded virus productivity in serum-free media. For transformed silkmoth cells maintained in serum-free media, the rate of BmNPV entry is enhanced by two orders of magnitude relative to the untransformed cells, while the rate of budded virus production is increased five-fold. The infectivity-enhancing effect can be also conferred to normal cells grown in serum-free media by addition of conditioned media from the transformed cells, which contain the secreted recombinant PP. Thus, PP substitutes for serum factors whose presence facilitates baculovirus entry into the cells. However, the effects of silkmoth-derived PP may be specific to the BmNPV-silkmoth system since little or no changes in viral infectivity are obtained by PP expression in Trichoplusia ni-derived High-Fivetrade mark cells grown in serum-free media and infected with a different baculovirus (AcNPV).
机译:杆状病毒载体构成了用于基因治疗应用的治疗性蛋白质生产和哺乳动物细胞转导的重要工具。进行此类应用的前提条件是将杆状病毒在其中繁殖的细胞系保持在不含潜在人类病原体的无血清培养基中。但是,在无血清培养基中,基于杆状病毒的系统的性能可能会大大降低。在本报告中,我们显示了家蚕来源的家蚕宿主细胞系,该家蚕细胞系已被促进蛋白(PP)基因转化而成,后者是家蚕来源的分泌因子,其包含脂质结合域,在无血清培养基中显示出对BmNPV感染的敏感性增加,并且芽病毒的生产率提高。对于保持在无血清培养基中的转化蚕蛾细胞,相对于未转化细胞,BmNPV进入的速率提高了两个数量级,而芽生病毒的产生速率提高了五倍。通过添加来自转化细胞的条件培养基(包含分泌的重组PP),还可以赋予在无血清培养基中生长的正常细胞以增强感染力。因此,PP替代了血清因子的存在,而血清因子的存在有助于杆状病毒进入细胞。然而,由于在无血清培养基中生长并感染了花粉虱的毛癣菌属的高Fivetrade标记细胞中的PP表达,蚕蛾的PP对BmNPV-silkmoth系统的作用可能是特异性的,因为病毒感染力几乎没有或没有变化。另一种杆状病毒(AcNPV)。

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