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Group V and X secretory phospholipase A2 prevents adenoviral infection in mammalian cells

机译:V和X组分泌型磷脂酶A2可预防哺乳动物细胞中的腺病毒感染

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摘要

sPLA2 (secretory phospholipase A2) enzymes have been implicated in various biological events, yet their precise physiological functions remain largely unresolved. In the present study we show that group V and X sPLA2s, which are two potent plasma membrane-acting sPLA2s, are capable of preventing host cells from being infected with an adenovirus. Bronchial epithelial cells and lung fibroblasts pre-expressing group V and X sPLA2s showed marked resistance to adenovirus-mediated gene delivery in a manner dependent on their catalytic activity. Although adenovirus particles were insensitive to recombinant group V and X sPLA2s, direct addition of these enzymes to 293A cells suppressed both number and size of adenovirus plaque formation. Group V and X sPLA2s retarded the entry of adenovirus into endosomes. Moreover, adenoviral infection was suppressed by LPC (lysophosphatidylcholine), a membrane-hydrolytic product of these sPLA2s. Thus hydrolysis of the plasma membrane by these sPLA2s may eventually lead to the protection of host cells from adenovirus entry. Given that group V and X sPLA2s are expressed in human airway epithelium and macrophages and that the expression of endogenous group V sPLA2 is upregulated by virus-related stimuli in these cells, our present results raise the possibility that group V and X sPLA2s may play a role in innate immunity against adenoviral infection in the respiratory tract.
机译:sPLA2(分泌型磷脂酶A2)酶已牵涉到各种生物学事件中,但其精确的生理功能仍未解决。在本研究中,我们显示V和X sPLA2组是两种有效的质膜作用sPLA2,它们能够防止宿主细胞被腺病毒感染。预先表达V和X sPLA2s的支气管上皮细胞和肺成纤维细胞对腺病毒介导的基因传递具有明显的抗性,具体取决于它们的催化活性。尽管腺病毒颗粒对重组V和X sPLA2s不敏感,但将这些酶直接添加到293A细胞中可抑制腺病毒斑块形成的数量和大小。 V组和X组sPLA2s抑制了腺病毒进入内体。此外,通过这些sPLA2的膜水解产物LPC(溶血磷脂酰胆碱)抑制了腺病毒感染。因此,这些sPLA2对质膜的水解可能最终导致保护宿主细胞免于腺病毒进入。鉴于V和X sPLA2s在人气道上皮和巨噬细胞中表达,并且内源性V sPLA2的表达被这些细胞中的病毒相关刺激上调,我们目前的研究结果增加了V和X sPLA2s可能发挥在对呼吸道腺病毒感染的天然免疫中发挥重要作用。

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