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Phenol-soluble Modulin α Peptide Toxins from aggressive Staphylococcus aureus induce rapid Formation of neutrophil extracellular Traps through a reactive Oxygen species-independent Pathway
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2017 (Engelska)Ingår i: Frontiers in Immunology, E-ISSN 1664-3224, Vol. 8, artikel-id 257Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Neutrophils have the ability to capture and kill microbes extracellularly through the formation of neutrophil extracellular traps (NETs). These are DNA and protein structures that neutrophils release extracellularly and are believed to function as a defense mechanism against microbes. The classic NET formation process, triggered by, e.g., bacteria, fungi, or by direct stimulation of protein kinase C through phorbol myristate acetate, is an active process that takes several hours and relies on the production of reactive oxygen species (ROS) that are further modified by myeloperoxidase (MPO). We show here that NET-like structures can also be formed by neutrophils after interaction with phenol-soluble modulin alpha (PSM alpha) that are cytotoxic membrane-disturbing peptides, secreted from community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA). The PSMa-induced NETs contained the typical protein markers and were able to capture microbes. The PSMa-induced NET structures were disintegrated upon prolonged exposure to DNase-positive S. aureus but not on exposure to DNase-negative Candida albicans. Opposed to classic NETosis, PSMa-triggered NET formation occurred very rapidly, independently of ROS or MPO, and was also manifest at 4 degrees C. These data indicate that rapid NETs release may result from cytotoxic membrane disturbance by PSMa peptides, a process that may be of importance for CA-MRSA virulence.

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2017. Vol. 8, artikel-id 257
Nyckelord [en]
community-acquired methicillin-resistant Staphylococcus aureus, PSM, NETs, ROS, FPR2, MPO, utrophil elastase, Papillon-Lefevre syndrome
Nationell ämneskategori
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)
Identifikatorer
URN: urn:nbn:se:umu:diva-133767DOI: 10.3389/fimmu.2017.00257ISI: 000395693300001PubMedID: 28337204Scopus ID: 2-s2.0-85017154415OAI: oai:DiVA.org:umu-133767DiVA, id: diva2:1092467
Tillgänglig från: 2017-05-03 Skapad: 2017-05-03 Senast uppdaterad: 2024-01-17Bibliografiskt granskad

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Stylianou, MariosUrban, Constantin F.

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Frontiers in Immunology
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)

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