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Novel aroylated phenylenediamine compounds enhance antimicrobial defense and maintain airway epithelial barrier integrity

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dc.contributor Háskóli Íslands
dc.contributor University of Iceland
dc.contributor.author Myszor, Iwona Teresa
dc.contributor.author Parveen, Zahida
dc.contributor.author Ottosson, Håkan
dc.contributor.author Bergman, Peter
dc.contributor.author Agerberth, Birgitta
dc.contributor.author Strömberg, Roger
dc.contributor.author Gudmundsson, Gudmundur H
dc.date.accessioned 2020-08-21T15:25:42Z
dc.date.available 2020-08-21T15:25:42Z
dc.date.issued 2019-05-08
dc.identifier.citation Myszor, I.T., Parveen, Z., Ottosson, H. et al. Novel aroylated phenylenediamine compounds enhance antimicrobial defense and maintain airway epithelial barrier integrity. Sci Rep 9, 7114 (2019). https://doi.org/10.1038/s41598-019-43350-z
dc.identifier.issn 2045-2322
dc.identifier.uri https://hdl.handle.net/20.500.11815/1995
dc.description Publisher's version (útgefin grein)
dc.description.abstract Aroylated phenylenediamines (APDs) are novel inducers of innate immunity enhancing cathelicidin gene expression in human bronchial epithelial cell lines. Here we present two newly developed APDs and aimed at defining the response and signaling pathways for these compounds with reference to innate immunity and antimicrobial peptide (AMP) expression. Induction was initially defined with respect to dose and time and compared with the APD Entinostat (MS-275). The induction applies to several innate immunity effectors, indicating that APDs trigger a broad spectrum of antimicrobial responses. The bactericidal effect was shown in an infection model against Pseudomonas aeruginosa by estimating bacteria entering cells. Treatment with a selected APD counteracted Pseudomonas mediated disruption of epithelial integrity. This double action by inducing AMPs and enhancing epithelial integrity for one APD compound is unique and taken as a positive indication for host directed therapy (HDT). The APD effects are mediated through Signal transducer and activator of transcription 3 (STAT3) activation. Utilization of induced innate immunity to fight infections can reduce antibiotic usage, might be effective against multidrug resistant bacteria and is in line with improved stewardship in healthcare.
dc.description.sponsorship Icelandic Center for Research (RANNÍS 173931) and University of Iceland research fund are acknowledged for support. Bryndís Valdimarsdóttir for advises on preparation of conditioned media and cell culture. Kristín Elísabet Alansdóttir for help with confocal microscopy and ImageJ analyses. Thanks to Náttúruverndarsjóður Pálma Jónssonar for early support of this project. We acknowledge Prof. Ronald G. Crystal and collaborators for generously providing us with the BCi-NS1.1 cell line. We thank Snæbjörn Pálsson for advices on statistical analysis.
dc.format.extent 7114
dc.language.iso en
dc.publisher Springer Science and Business Media LLC
dc.relation.ispartofseries Scientific Reports;9(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Antimicrobial Peptide LL 37
dc.subject Cell signalling
dc.subject Innate immunity
dc.subject Frumulíffræði
dc.subject Ónæmiserfðafræði
dc.title Novel aroylated phenylenediamine compounds enhance antimicrobial defense and maintain airway epithelial barrier integrity
dc.type info:eu-repo/semantics/article
dcterms.license This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
dc.description.version Peer reviewed
dc.identifier.journal Scientific Reports
dc.identifier.doi 10.1038/s41598-019-43350-z
dc.contributor.department Lífvísindasetur (HÍ)
dc.contributor.department Biomedical Center (UI)
dc.contributor.school Verkfræði- og náttúruvísindasvið (HÍ)
dc.contributor.school School of Engineering and Natural Sciences (UI)


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