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dc.contributor.authorHosseinzadeh, Ava
dc.contributor.authorThompson, Paul R
dc.contributor.authorSegal, Brahm H.
dc.contributor.authorUrban, Constantin F.
dc.date2022-08-11T08:11:00.000
dc.date.accessioned2022-08-23T17:28:01Z
dc.date.available2022-08-23T17:28:01Z
dc.date.issued2016-11-01
dc.date.submitted2017-02-17
dc.identifier.citationJ Leukoc Biol. 2016 Nov;100(5):1105-1112. Epub 2016 Jun 16. <a href="https://doi.org/10.1189/jlb.3AB0815-379RR">Link to article on publisher's site</a>
dc.identifier.issn0741-5400 (Linking)
dc.identifier.doi10.1189/jlb.3AB0815-379RR
dc.identifier.pmid27312847
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49991
dc.description.abstractNETs serve to ensnare and kill microbial pathogens. However, NETs can at the same time contribute to tissue damage and excessive inflammation. Nicotine is a major toxic agent and has been associated with exacerbated inflammatory diseases. The current study aimed at investigating the role of nicotine, the addictive component of tobacco and electronic cigarettes, on triggering NET formation. We report that nicotine induces neutrophils to release NETs in a dose-dependent manner. Nicotine-induced NET formation is mediated via nicotine acetylcholine receptors, depends on Akt and PAD4 activation, but is Nox2-independent, as demonstrated by pharmacological inhibition of Nox2 and by use of Nox2-deficient mouse neutrophils. These findings demonstrate that nicotine induces NETs, which may in turn contribute to smoking-related diseases.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=27312847&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttps://doi.org/10.1189/jlb.3AB0815-379RR
dc.subjectneutrophil extracellular traps
dc.subjectNETs
dc.subjectBiochemistry
dc.subjectCell Biology
dc.subjectEnzymes and Coenzymes
dc.subjectMedicinal-Pharmaceutical Chemistry
dc.titleNicotine induces neutrophil extracellular traps
dc.typeJournal Article
dc.source.journaltitleJournal of leukocyte biology
dc.source.volume100
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/thompson/110
dc.identifier.contextkey9705377
html.description.abstract<p>NETs serve to ensnare and kill microbial pathogens. However, NETs can at the same time contribute to tissue damage and excessive inflammation. Nicotine is a major toxic agent and has been associated with exacerbated inflammatory diseases. The current study aimed at investigating the role of nicotine, the addictive component of tobacco and electronic cigarettes, on triggering NET formation. We report that nicotine induces neutrophils to release NETs in a dose-dependent manner. Nicotine-induced NET formation is mediated via nicotine acetylcholine receptors, depends on Akt and PAD4 activation, but is Nox2-independent, as demonstrated by pharmacological inhibition of Nox2 and by use of Nox2-deficient mouse neutrophils. These findings demonstrate that nicotine induces NETs, which may in turn contribute to smoking-related diseases.</p>
dc.identifier.submissionpaththompson/110
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages1105-1112


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