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Interleukin 4 induces the expression of inducible nitric oxide synthase in eosinophils

dc.contributor.authorPaoliello-Paschoalatoa, A. B.
dc.contributor.authorOliveira, SHP
dc.contributor.authorCunha, F. Q.
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:24:27Z
dc.date.available2014-05-20T15:24:27Z
dc.date.issued2005-05-07
dc.description.abstractWe investigated the effects of the Th-2-like cytokines IL-4 and IL-13 and of IL-10 on the induction of iNOS and NO production in rat eosinophils. Addition of mIL-4 to the eosinophil culture increased iNOS activity and nitrite production but did not improve the stimulatory effect of IFN-gamma and LPS. in contrast to eosinophils, addition of mIL-4 to macrophage cultures inhibited the iNOS expression and nitrite production induced by IFN-gamma plus LPS. Addition of mIL-13 to the eosinophil cultures did not significantly change iNOS activity and nitrite production in cells stimulated or not with IFN-gamma plus LPS. on the other hand, IL-13 inhibited iNOS activity in IFN-gamma plus LPS-stimulated macrophages. In the presence of IL-10, iNOS activity in non-stimulated eosinophil or macrophage cultures was not significantly altered, but the enzyme expression was inhibited in IFN-gamma plus LPS-stimulated eosinophils or macrophages. The production of nitrite by eosinophils stimulated by IFN-gamma plus LPS was inhibited by the presence of IL-10 in the medium. In conclusion, eosinophils might exhibit differential modulation of the L-arginine/iNOS pathway depending on the profile of Th-2 cytokines produced during allergic diseases. IL-4 appears to be an important Th2 cytokine involved in the induction of the L-arginine/iNOS pathway in eosinophils. (c) 2005 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniv São Paulo, Fac Med Ribeirao Preto, Dept Pharmacol, BR-14049900 Ribeirao Preto, SP, Brazil
dc.description.affiliationDepartment of Basic Science, School of Dentistry, State University of São Paulo, Araçatuba
dc.description.affiliationUnespDepartment of Basic Science, School of Dentistry, State University of São Paulo, Araçatuba
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipPrograma de Apoio aos Núcleos de Excelência (PRONEX)
dc.format.extent116-124
dc.identifierhttp://dx.doi.org/10.1016/j.cyto.2005.01.001
dc.identifier.citationCytokine. London: Academic Press Ltd Elsevier B.V. Ltd, v. 30, n. 3, p. 116-124, 2005.
dc.identifier.doi10.1016/j.cyto.2005.01.001
dc.identifier.issn1043-4666
dc.identifier.lattes8905977598945667
dc.identifier.urihttp://hdl.handle.net/11449/35065
dc.identifier.wosWOS:000228760900004
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofCytokine
dc.relation.ispartofjcr3.514
dc.relation.ispartofsjr1,433
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjecteosinophilspt
dc.subjectIL-4pt
dc.subjectIL-13pt
dc.subjectIL-10pt
dc.subjectnitric oxidept
dc.titleInterleukin 4 induces the expression of inducible nitric oxide synthase in eosinophilsen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublication8b3335a4-1163-438a-a0e2-921a46e0380d
relation.isOrgUnitOfPublication.latestForDiscovery8b3335a4-1163-438a-a0e2-921a46e0380d
unesp.author.lattes8905977598945667
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araçatubapt
unesp.departmentCiências Básicas - FOApt

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