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Leppkes, M.* ; Maueroeder, C.* ; Hirth, S.* ; Nowecki, S.* ; Guenther, C.* ; Billmeier, U.* ; Paulus, S.* ; Biermann, M.* ; Munoz, L.E.* ; Hoffmann, M.* ; Wildner, D.* ; Croxford, A.L.* ; Waisman, A.* ; Mowen, K.* ; Jenne, D.* ; Krenn, V.* ; Mayerle, J.* ; Lerch, M.M.* ; Schett, G.* ; Wirtz, S.* ; Neurath, M.F.* ; Hermann, M.* ; Becker, C.*

Externalized decondensed neutrophil chromatin occludes pancreatic ducts and drives pancreatitis.

Nat. Commun. 7:10973 (2016)
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Open Access Gold möglich sobald Verlagsversion bei der ZB eingereicht worden ist.
Ductal occlusion has been postulated to precipitate focal pancreatic inflammation, while the nature of the primary occluding agents has remained elusive. Neutrophils make use of histone citrullination by peptidyl arginine deiminase-4 (PADI4) in contact to particulate agents to extrude decondensed chromatin as neutrophil extracellular traps (NETs). In high cellular density, NETs form macroscopically visible aggregates. Here we show that such aggregates form inside pancreatic ducts in humans and mice occluding pancreatic ducts and thereby driving pancreatic inflammation. Experimental models indicate that PADI4 is critical for intraductal aggregate formation and that PADI4-deficiency abrogates disease progression. Mechanistically, we identify the pancreatic juice as a strong instigator of neutrophil chromatin extrusion. Characteristic single components of pancreatic juice, such as bicarbonate ions and calcium carbonate crystals, induce aggregated NET formation. Ductal occlusion by aggregated NETs emerges as a pathomechanism with relevance in a plethora of inflammatory conditions involving secretory ducts.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Extracellular Trap Formation; Cathepsin-b; Mouse Model; Autoimmune Pancreatitis; Biliary Pancreatitis; Trypsin Activation; Tissue-damage; Lung Injury; In-vivo; Mice
Sprache englisch
Veröffentlichungsjahr 2016
HGF-Berichtsjahr 0
ISSN (print) / ISBN 2041-1723
e-ISSN 2041-1723
Zeitschrift Nature Communications
Quellenangaben Band: 7, Heft: , Seiten: , Artikelnummer: 10973 Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Lung Health and Immunity (LHI)
POF Topic(s) 30202 - Environmental Health
Forschungsfeld(er) Lung Research
PSP-Element(e) G-501600-005
DOI 10.1038/ncomms10973
WOS ID WOS:000372019600001
Erfassungsdatum 2016-04-02
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