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dc.contributor.authorGomes, Alessandra Ferreira-
dc.contributor.authorMagalhães, Kelly Grace-
dc.contributor.authorRodrigues, Renata M.-
dc.contributor.authorCarvalho, Laís de-
dc.contributor.authorMolinaro, Raphael-
dc.contributor.authorBozza, Patrícia Torres-
dc.contributor.authorBarbosa, Helene Santos-
dc.date.accessioned2017-06-28T14:30:28Z-
dc.date.available2017-06-28T14:30:28Z-
dc.date.issued2014-01-23-
dc.identifier.citationGOMES, Alessandra Ferreira et al. Toxoplasma gondii-skeletal muscle cells interaction increases lipid droplet biogenesis and positively modulates the production of IL-12, IFN-g and PGE2. Parasites & Vectors, v. 7, Article 47, 23 jan. 2014. Disponível em: <https://parasitesandvectors.biomedcentral.com/articles/10.1186/1756-3305-7-47>. Acesso em: 26 jun. 2017. doi: https://parasitesandvectors.biomedcentral.com/articles/10.1186/1756-3305-7-47.pt_BR
dc.identifier.urihttp://repositorio.unb.br/handle/10482/23769-
dc.language.isoInglêspt_BR
dc.publisherBioMed Centralpt_BR
dc.rightsAcesso Abertopt_BR
dc.titleToxoplasma gondii-skeletal muscle cells interaction increases lipid droplet biogenesis and positively modulates the production of IL-12, IFN-g and PGE2pt_BR
dc.typeArtigopt_BR
dc.subject.keywordToxoplasma gondiipt_BR
dc.subject.keywordLipídiospt_BR
dc.subject.keywordInfecçãopt_BR
dc.subject.keywordCitocinaspt_BR
dc.subject.keywordProstaglandinapt_BR
dc.rights.license© 2014 Gomes et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.pt_BR
dc.identifier.doihttps://dx.doi.org/10.1186/1756-3305-7-47pt_BR
dc.description.abstract1Background: The interest in the mechanisms involved in Toxoplasma gondii lipid acquisition has steadily increased during the past few decades, but it remains not completely understood. Here, we investigated the biogenesis and the fate of lipid droplets (LD) of skeletal muscle cells (SkMC) during their interaction with T. gondii by confocal and electron microscopy. We also evaluated whether infected SkMC modulates the production of prostaglandin E2 (PGE2), cytokines interleukin-12 (IL-12) and interferon-gamma (INF-g), and also the cyclooxygenase-2 (COX-2) gene induction. Methods: Primary culture of skeletal muscle cells were infected with tachyzoites of T. gondii and analysed by confocal microscopy for observation of LD. Ultrastructural cytochemistry was also used for lipid and sarcoplasmatic reticulum (SR) detection. Dosage of cytokines (IL-12 and INF-g) by ELISA technique and enzyme-linked immunoassay (EIA) for PGE2 measurement were employed. The COX-2 gene expression analysis was performed by real time reverse transcriptase polymerase chain reaction (qRT-PCR). Results: We demonstrated that T. gondii infection of SkMC leads to increase in LD number and area in a time course dependent manner. Moreover, the ultrastructural analysis demonstrated that SR and LD are in direct contact with parasitophorous vacuole membrane (PVM), within the vacuolar matrix, around it and interacting directly with the membrane of parasite, indicating that LD are recruited and deliver their content inside the parasitophorous vacuole (PV) in T. gondii-infected SkMC. We also observed a positive modulation of the production of IL-12 and IFN-g, increase of COX-2 mRNA levels in the first hour of T. gondii-SkMC interaction and an increase of prostaglandin E2 (PGE2) synthesis from 6 h up to 48 h of infection. Conclusions: Taken together, the close association between SR and LD with PV could represent a source of lipids as well as other nutrients for the parasite survival, and together with the increased levels of IL-12, INF-g and inflammatory indicators PGE2 and COX-2 might contribute to the establishment and maintenance of chronic phase of the T. gondii infection in muscle cell.pt_BR
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