Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/1362
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dc.contributor.authorJorjão, Adeline Lacerdapt_BR
dc.contributor.authorOliveira, Felipe Eduardo dept_BR
dc.contributor.authorLeão, Mariella Vieira Pereirapt_BR
dc.contributor.authorCarvalho, Cláudio Antonio Talgept_BR
dc.contributor.authorJorge, Antonio Olavo Cardosopt_BR
dc.contributor.authorOliveira, Luciane Dias dept_BR
dc.date.accessioned2019-09-11T20:51:31Z-
dc.date.available2019-09-11T20:51:31Z-
dc.date.issued2015-
dc.citation.volume2015pt_BR
dc.identifier.doi10.1155/2015/716749pt_BR
dc.identifier.issn23566140-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84948845306&doi=10.1155%2f2015%2f716749&partnerID=40&md5=aadcb001b39e3277fdc4351d9cedf5b0-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/1362-
dc.description716749pt_BR
dc.description.abstractThis study aimed to evaluate the capacity of Lactobacillus rhamnosus and/or its products to induce the synthesis of cytokines (TNF-α, IL-1β, IL-4, IL-6, IL-10, and IL-12) by mouse macrophages (RAW 264.7). Three microorganism preparations were used: live L. rhamnosus (LLR) suspension, heat-killed L. rhamnosus (HKLR) suspension, and the supernatant of a heat-killed L. rhamnosus (SHKLR) suspension, which were cultured with macrophages (37°C, 5% CO2) for 2 h and 30 min. After that, cells were cultured for 16 h. The supernatants were used for the quantitation of cytokines, by ELISA. The results were compared with the synthesis induced by lipopolysaccharide (LPS) and analysed, using ANOVA and Tukey test, 5%. LLR and HKLR groups were able to significantly increase the production of TNF-α, IL-6, and IL-10 (P < 0. 05). SHKLR also significantly increased the production of TNF-α and IL-10 (P < 0. 05) but not IL-6 (P > 0. 05). All the L. rhamnosus suspensions were not able to produce detectable levels of IL-1β or significant levels of IL-4 and IL-12 (P > 0. 05). In conclusion, live and heat-killed L. rhamnosus suspensions were able to induce the synthesis of different cytokines with proinflammatory (TNF-α and IL-6) or regulatory (IL-10) functions, suggesting the role of strain L. rhamnosus ATCC 7469 in the modulation or in the stimulation of immune responses. © 2015 Adeline Lacerda Jorjão et al.en
dc.description.provenanceMade available in DSpace on 2019-09-11T20:51:31Z (GMT). No. of bitstreams: 0 Previous issue date: 2015en
dc.languageInglêspt_BR
dc.publisherHindawi Publishing Corporation-
dc.relation.ispartofScientific World Journal-
dc.rightsAcesso Abertopt_BR
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceScopuspt_BR
dc.subject.othercytokineen
dc.subject.otherinterleukin 10en
dc.subject.otherinterleukin 12en
dc.subject.otherinterleukin 1betaen
dc.subject.otherinterleukin 4en
dc.subject.otherinterleukin 6en
dc.subject.otherlipopolysaccharideen
dc.subject.othertumor necrosis factor alphaen
dc.subject.othercytokineen
dc.subject.otherprobiotic agenten
dc.subject.otheranimal cellen
dc.subject.otherArticleen
dc.subject.otherbacterium cultureen
dc.subject.othercontrolled studyen
dc.subject.othercytokine productionen
dc.subject.othercytokine releaseen
dc.subject.otherenzyme linked immunosorbent assayen
dc.subject.otherin vitro studyen
dc.subject.otherLactobacillus rhamnosusen
dc.subject.othermacrophageen
dc.subject.othermouseen
dc.subject.othernonhumanen
dc.subject.othersynthesisen
dc.subject.otheranimalen
dc.subject.othercell lineen
dc.subject.otherdrug effectsen
dc.subject.otherLactobacillus rhamnosusen
dc.subject.othermacrophageen
dc.subject.othermetabolismen
dc.subject.othermicrobiologyen
dc.subject.otherpathogenicityen
dc.subject.otherAnimalsen
dc.subject.otherCell Lineen
dc.subject.otherCytokinesen
dc.subject.otherLactobacillus rhamnosusen
dc.subject.otherMacrophagesen
dc.subject.otherMiceen
dc.subject.otherProbioticsen
dc.titleLive and Heat-Killed Lactobacillus rhamnosus ATCC 7469 May Induce Modulatory Cytokines Profiles on Macrophages RAW 264.7en
dc.typeArtigo de Periódicopt_BR
dc.description.affiliationJorjão, A.L., Department of Biosciences and Oral Diagnosis, Laboratory of Microbiology and Immunology, Institute of Science and Technology, Universidade Estadual Paulista (UNESP), Avenida Engenheiro Francisco José Longo, São José dos Campos, SP, 12245-000, Brazil-
dc.description.affiliationDe Oliveira, F.E., Department of Biosciences and Oral Diagnosis, Laboratory of Microbiology and Immunology, Institute of Science and Technology, Universidade Estadual Paulista (UNESP), Avenida Engenheiro Francisco José Longo, São José dos Campos, SP, 12245-000, Brazil-
dc.description.affiliationLeão, M.V.P., Bioscience Basic Institute, University of Taubaté, Street Expedicionário Ernesto Pereira 3, Taubaté, SP, 12020-130, Brazil-
dc.description.affiliationCarvalho, C.A.T., Department of Restorative Dentistry, Institute of Science and Technology, Universidade Estadual Paulista (UNESP), Avenida Engenheiro Francisco José Longo, São José dos Campos, SP, 12245-000, Brazil-
dc.description.affiliationJorge, A.O.C., Department of Biosciences and Oral Diagnosis, Laboratory of Microbiology and Immunology, Institute of Science and Technology, Universidade Estadual Paulista (UNESP), Avenida Engenheiro Francisco José Longo, São José dos Campos, SP, 12245-000, Brazil-
dc.description.affiliationDe Oliveira, L.D., Department of Biosciences and Oral Diagnosis, Laboratory of Microbiology and Immunology, Institute of Science and Technology, Universidade Estadual Paulista (UNESP), Avenida Engenheiro Francisco José Longo, São José dos Campos, SP, 12245-000, Brazil-
dc.identifier.scopus2-s2.0-84948845306-
dc.contributor.scopus55220155200pt_BR
dc.contributor.scopus56178280200pt_BR
dc.contributor.scopus8366375600pt_BR
dc.contributor.scopus8308307000pt_BR
dc.contributor.scopus7005222026pt_BR
dc.contributor.scopus13003558900pt_BR
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