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dc.contributor.authorKenny, Elaine F.
dc.contributor.authorHerzig, Alf
dc.contributor.authorKrüger, Renate
dc.contributor.authorMuth, Aaron
dc.contributor.authorMondal, Santanu
dc.contributor.authorThompson, Paul R
dc.contributor.authorBrinkmann, Volker
dc.contributor.authorVon Bernuth, Horst
dc.contributor.authorZychlinsky, Arturo
dc.date2022-08-11T08:11:00.000
dc.date.accessioned2022-08-23T17:28:02Z
dc.date.available2022-08-23T17:28:02Z
dc.date.issued2017-06-02
dc.date.submitted2017-06-19
dc.identifier.citationElife. 2017 Jun 2;6. pii: e24437. doi: 10.7554/eLife.24437. [Epub ahead of print] <a href="https://doi.org/10.7554/eLife.24437">Link to article on publisher's website</a>
dc.identifier.issn2050-084X
dc.identifier.doi10.7554/eLife.24437
dc.identifier.pmid28574339
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49995
dc.description.abstractNeutrophils release neutrophil extracellular traps (NETs) which ensnare pathogens and have pathogenic functions in diverse diseases. We examined the NETosis pathways induced by five stimuli; PMA, the calcium ionophore A23187, nigericin, Candida albicans and Group B Streptococcus. We studied NET production in neutrophils from healthy donors with inhibitors of molecules crucial to PMA induced NETs including protein kinase C, calcium, reactive oxygen species, the enzymes myeloperoxidase (MPO) and neutrophil elastase. Additionally, neutrophils from chronic granulomatous disease patients, carrying mutations in the NADPH oxidase complex or a MPO-deficient patient were examined. We show that PMA, C. albicans and GBS use a related pathway for NET induction whereas ionophores require an alternative pathway but that NETs produced by all stimuli are proteolytically active, kill bacteria and composed mainly of chromosomal DNA. Thus, we demonstrate that NETosis occurs through several signalling mechanisms, suggesting that extrusion of NETs is important in host defence.
dc.language.isoen_US
dc.publishereLife Sciences
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=28574339&dopt=Abstract">Link to article in PubMed</a>
dc.rights© 2017, Kenny et al.
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectcell biology
dc.subjecthuman
dc.subjectimmunology
dc.subjectBiochemistry
dc.subjectCell Biology
dc.subjectEnzymes and Coenzymes
dc.subjectImmunology and Infectious Disease
dc.subjectMedicinal-Pharmaceutical Chemistry
dc.subjectTherapeutics
dc.titleDiverse stimuli engage different neutrophil extracellular trap pathways
dc.typeAccepted Manuscript
dc.source.journaltitleElife
dc.source.volume6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1116&amp;context=thompson&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/thompson/114
dc.legacy.embargo2017-06-19T00:00:00-07:00
dc.identifier.contextkey10319105
refterms.dateFOA2022-08-23T17:28:02Z
html.description.abstract<p>Neutrophils release neutrophil extracellular traps (NETs) which ensnare pathogens and have pathogenic functions in diverse diseases. We examined the NETosis pathways induced by five stimuli; PMA, the calcium ionophore A23187, nigericin, Candida albicans and Group B Streptococcus. We studied NET production in neutrophils from healthy donors with inhibitors of molecules crucial to PMA induced NETs including protein kinase C, calcium, reactive oxygen species, the enzymes myeloperoxidase (MPO) and neutrophil elastase. Additionally, neutrophils from chronic granulomatous disease patients, carrying mutations in the NADPH oxidase complex or a MPO-deficient patient were examined. We show that PMA, C. albicans and GBS use a related pathway for NET induction whereas ionophores require an alternative pathway but that NETs produced by all stimuli are proteolytically active, kill bacteria and composed mainly of chromosomal DNA. Thus, we demonstrate that NETosis occurs through several signalling mechanisms, suggesting that extrusion of NETs is important in host defence.</p>
dc.identifier.submissionpaththompson/114
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pagese24437


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© 2017, Kenny et al.
Except where otherwise noted, this item's license is described as © 2017, Kenny et al.