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Invasion of epithelial mammalian cells by Paracoccidioides brasiliensis leads to cytoskeletal rearrangement and apoptosis of the host cell

dc.contributor.authorMendes-Giannini, Maria José Soares [UNESP]
dc.contributor.authorHanna, S. A.
dc.contributor.authorSilva, J. L. M. da
dc.contributor.authorAndreotti, P. F.
dc.contributor.authorVincenzi, L. R.
dc.contributor.authorBenard, G.
dc.contributor.authorLenzi, H. L.
dc.contributor.authorSoares, Christiane Pienna [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionInst Oswaldo Cruz
dc.date.accessioned2014-05-20T13:24:35Z
dc.date.available2014-05-20T13:24:35Z
dc.date.issued2004-08-01
dc.description.abstractParacoccidioides brasiliensis (Pb) yeast cells can enter mammalian cells and probably manipulate the host cell environment to favor their own growth and survival. We studied the uptake of strain Pb 18 into A549 lung and Vero epithelial cells, with an emphasis on the repercussions in the cytoskeleton and the apoptosis of host cells. Cytoskeleton components of the host cells, such as actin and tubulin, were involved in the P. brasiliensis invasion process. Cytochalasin D and colchicine treatment substantially reduced invasion, indicating the functional participation of microfilaments (MFs) and microtubules (MTs) in this mechanism. Cytokeratin could also play a role in the P. brasiliensis interaction with the host. Gp43 was recognized by anti-actin and anti-cytokeratin antibodies, but not by anti-tubulin. The apoptosis induced by this fungus in infected epithelial cells was demonstrated by various techniques: TUNEL, DNA fragmentation and Bak and Bcl-2 immunocytochemical expression. DNA fragmentation was observed in infected cells but not in uninfected ones, by both TUNEL and gel electrophoresis methods. Moreover, Bcl-2 and Bak did not show any differences until 24 h after infection of cells, suggesting a competitive mechanism that allows persistence of infection. Overexpression of Bak was observed after 48 h, indicating the loss of competition between death and survival signals. In conclusion, the mechanisms of invasion of host cells, persistence within them, and the subsequent induction of apoptosis of such cells may explain the efficient dissemination of P. brasiliensis. (C) 2004 Published by Elsevier SAS.en
dc.description.affiliationUNESP, Dept Anal Clin, Fac Ciências Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUSP, Lab Alergia & Immunol Clin & Expt & Clin Doencas, Fac Med, BR-09500900 São Paulo, Brazil
dc.description.affiliationInst Oswaldo Cruz, Dept Patol, BR-20001 Rio de Janeiro, Brazil
dc.description.affiliationUnespUNESP, Dept Anal Clin, Fac Ciências Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.format.extent882-891
dc.identifierhttp://dx.doi.org/10.1016/j.micinf.2004.05.005
dc.identifier.citationMicrobes and Infection. Amsterdam: Elsevier B.V., v. 6, n. 10, p. 882-891, 2004.
dc.identifier.doi10.1016/j.micinf.2004.05.005
dc.identifier.issn1286-4579
dc.identifier.lattes1768025290373669
dc.identifier.orcid0000-0002-8059-0826
dc.identifier.orcid0000-0003-1740-7360
dc.identifier.urihttp://hdl.handle.net/11449/7674
dc.identifier.wosWOS:000223377200002
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofMicrobes and Infection
dc.relation.ispartofjcr2.924
dc.relation.ispartofsjr1,205
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectParacoccidioides brasiliensispt
dc.subjectcytoskeletonpt
dc.subjectinvasionpt
dc.subjectapoptosispt
dc.subjecthost-cell biologypt
dc.titleInvasion of epithelial mammalian cells by Paracoccidioides brasiliensis leads to cytoskeletal rearrangement and apoptosis of the host cellen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes1768025290373669[8]
unesp.author.orcid0000-0002-8059-0826[1]
unesp.author.orcid0000-0003-1740-7360[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt

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