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
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