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首页> 外文期刊>The biochemical journal >Group V and X secretory phospholipase A2 prevents adenoviral infection in mammalian cells
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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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psPLAsub2/sub (secretory phospholipase Asub2/sub) 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 sPLAsub2/subs, which are two potent plasma membrane-acting sPLAsub2/subs, are capable of preventing host cells from being infected with an adenovirus. Bronchial epithelial cells and lung fibroblasts pre-expressing group V and X sPLAsub2/subs 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 sPLAsub2/subs, direct addition of these enzymes to 293A cells suppressed both number and size of adenovirus plaque formation. Group V and X sPLAsub2/subs retarded the entry of adenovirus into endosomes. Moreover, adenoviral infection was suppressed by LPC (lysophosphatidylcholine), a membrane-hydrolytic product of these sPLAsub2/subs. Thus hydrolysis of the plasma membrane by these sPLAsub2/subs may eventually lead to the protection of host cells from adenovirus entry. Given that group V and X sPLAsub2/subs are expressed in human airway epithelium and macrophages and that the expression of endogenous group V sPLAsub2/sub is upregulated by virus-related stimuli in these cells, our present results raise the possibility that group V and X sPLAsub2/subs may play a role in innate immunity against adenoviral infection in the respiratory tract./p
机译:> sPLA 2 (分泌型磷脂酶A 2 )酶与各种生物学事件有关,但其精确的生理功能仍未得到解决。在本研究中,我们表明V和X sPLA 2 s是两个有效的质膜作用sPLA 2 s,能够防止宿主细胞被感染用腺病毒。预先表达V和X sPLA 2 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,这取决于它们的催化活性。尽管腺病毒颗粒对重组组V和X sPLA 2 不敏感,但将这些酶直接加入293A细胞可抑制腺病毒斑块形成的数量和大小。 V组和X sPLA 2 阻碍了腺病毒进入内体。此外,腺病毒感染被LPC(溶血磷脂酰胆碱)抑制,这是这些sPLA 2 的膜水解产物。因此,这些sPLA 2 对质膜的水解可能最终导致宿主细胞免受腺病毒进入的保护。鉴于V和X sPLA 2 s在人气道上皮和巨噬细胞中表达,并且内源性V sPLA 2 的表达在这些呼吸道中被病毒相关刺激上调目前的研究结果提示,V和X sPLA 2 s组可能在抵抗呼吸道腺病毒感染的先天免疫中发挥作用。

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