Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/67267

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dc.contributor.authorGressler, Markuspor
dc.contributor.authorHeddergott, Christophpor
dc.contributor.authorN'Go, Inés C.por
dc.contributor.authorRenga, Giorgiapor
dc.contributor.authorOikonomou, Vasilispor
dc.contributor.authorMoretti, Silviapor
dc.contributor.authorCoddeville, Bernadettepor
dc.contributor.authorGaifem, Joanapor
dc.contributor.authorSilvestre, Ricardo Jorge Lealpor
dc.contributor.authorRomani, Luiginapor
dc.contributor.authorLatgé, Jean-Paulpor
dc.contributor.authorFontaine, Thierrypor
dc.date.accessioned2020-10-02T16:32:56Z-
dc.date.available2020-10-02T16:32:56Z-
dc.date.issued2019-11-
dc.identifier.citationFontaine, T., Gressler, M., Heddergott, C., Renga, G., et. al. (2019). Definition of the anti-inflammatory oligosaccharides derived from the galactosaminogalactan (GAG) from Aspergillus fumigatus. Frontiers in cellular and infection microbiology, 9, 365por
dc.identifier.issn2235-2988por
dc.identifier.urihttps://hdl.handle.net/1822/67267-
dc.description.abstractGalactosaminogalactan (GAG) is an insoluble aminosugar polymer produced by Aspergillus fumigatus and has anti-inflammatory properties. Here, the minimum glycosidic sequences required for the induction of IL-1Ra by peripheral blood mononuclear cells (PBMCs) was investigated. Using chemical degradation of native GAG to isolate soluble oligomers, we have found that the de-N-acetylation of galactosamine residues and the size of oligomer are critical for the in vitro immune response. A minimal oligomer size of 20 galactosamine residues is required for the anti-inflammatory response but the presence of galactose residues is not necessary. In a Dextran sulfate induced colitis mouse model, a fraction of de-N-acetylated oligomers of 13 < dp < 20 rescue inflammatory damage like the native GAG polymer in an IL-1Ra dependent pathway. Our results demonstrate the therapeutic suitability of water-soluble GAG oligosaccharides in IL-1 mediated hyper-inflammatory diseases and suggest that α-1,4-galactosamine oligomers chemically synthesized could represent new anti-inflammatory glycodrugs.por
dc.description.sponsorshipAviesan project Aspergillus, the French Government's Investissement d'Avenir program, Laboratoire d'Excellence Integrative Biology of Emerging Infectious Diseases (Grant No ANR-10-LABX-62-IBEID), la Fondation pour la Recherche Médicale (DEQ20150331722 LATGE Equipe FRM 2015). RS thanks Fundação para a Ciência e Tecnologia (FCT) contract IF/00021/2014por
dc.language.isoengpor
dc.publisherFrontiers Mediapor
dc.rightsopenAccesspor
dc.subjectAnimalspor
dc.subjectAnti-Inflammatory Agentspor
dc.subjectAspergillus fumigatuspor
dc.subjectColitispor
dc.subjectDextran Sulfatepor
dc.subjectHumanspor
dc.subjectInterleukin 1 Receptor Antagonist Proteinpor
dc.subjectLeukocytes, Mononuclearpor
dc.subjectMicepor
dc.subjectOligosaccharidespor
dc.subjectPolysaccharidespor
dc.subjectPolysaccharides, Bacterialpor
dc.subjectSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionizationpor
dc.subjectGalactosaminogalactanpor
dc.subjectIL-Rapor
dc.subjectAnti-inflammatory responsepor
dc.subjectGlycodrugpor
dc.titleDefinition of the anti-inflammatory oligosaccharides derived from the galactosaminogalactan (GAG) from Aspergillus fumigatuspor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttps://www.frontiersin.org/articles/10.3389/fcimb.2019.00365/fullpor
oaire.citationVolume9por
dc.identifier.eissn2235-2988-
dc.identifier.doi10.3389/fcimb.2019.00365por
dc.identifier.pmid31781511por
dc.subject.fosCiências Médicas::Medicina Básicapor
dc.subject.wosScience & Technologypor
sdum.journalFrontiers in Cellular and Infection Microbiologypor
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

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