Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/267824 |
Resumo: | Cryptococcus neoformans and Cryptococcus gattii are the etiological agents of cryptococcosis, a high mortality disease. The development of such disease depends on the interaction of fungal cells with macrophages, in which they can reside and replicate. In order to dissect the molecular mechanisms by which cryptococcal cells modulate the activity of macrophages, a genome-scale comparative analysis of transcriptional changes in macrophages exposed to Cryptococcus spp. was conducted. Altered expression of nearly 40 genes was detected in macrophages exposed to cryptococcal cells. The major processes were associated with the mTOR pathway, whose associated genes exhibited decreased expression in macrophages incubated with cryptococcal cells. Phosphorylation of p70S6K and GSK-3β was also decreased in macrophages incubated with fungal cells. In this way, Cryptococci presence could drive the modulation of mTOR pathway in macrophages possibly to increase the survival of the pathogen. |
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Piffer, Alicia CorbelliniSantos, Francine Melise dosThomé, Marcos PauloRosa, Camila Diehl daGarcia, Ane Wichine AcostaKinskovski, Uriel PerinSchneider, Rafael de OliveiraGerber, Alexandra LehmkuhlFeltes, Bruno CésarSchrank, AugustoVasconcelos, Ana Tereza Ribeiro deLenz, GuidoSilva, Lívia Kmetzsch Rosa eVainstein, Marilene HenningStaats, Charley Christian2023-11-30T03:23:26Z20211415-4757http://hdl.handle.net/10183/267824001172711Cryptococcus neoformans and Cryptococcus gattii are the etiological agents of cryptococcosis, a high mortality disease. The development of such disease depends on the interaction of fungal cells with macrophages, in which they can reside and replicate. In order to dissect the molecular mechanisms by which cryptococcal cells modulate the activity of macrophages, a genome-scale comparative analysis of transcriptional changes in macrophages exposed to Cryptococcus spp. was conducted. Altered expression of nearly 40 genes was detected in macrophages exposed to cryptococcal cells. The major processes were associated with the mTOR pathway, whose associated genes exhibited decreased expression in macrophages incubated with cryptococcal cells. Phosphorylation of p70S6K and GSK-3β was also decreased in macrophages incubated with fungal cells. In this way, Cryptococci presence could drive the modulation of mTOR pathway in macrophages possibly to increase the survival of the pathogen.application/pdfengGenetics and molecular biology. Ribeirão Preto. Vol. 44, no. 3 (2021), e20200390, 13 p.Cryptococcus neoformansCryptococcus gattiiMacrófagosRNAMacrophageCryptococcusRNAseqmTOR pathwayInteratomic networksTranscriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cellsinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001172711.pdf.txt001172711.pdf.txtExtracted Texttext/plain58620http://www.lume.ufrgs.br/bitstream/10183/267824/2/001172711.pdf.txt3de5dd33ca1c009f0657c64fddd86a37MD52ORIGINAL001172711.pdfTexto completo (inglês)application/pdf4878372http://www.lume.ufrgs.br/bitstream/10183/267824/1/001172711.pdfe9a9adfcc8f2ab813ff9b43de0faf6acMD5110183/2678242024-05-01 06:50:51.05983oai:www.lume.ufrgs.br:10183/267824Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-05-01T09:50:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
title |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
spellingShingle |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells Piffer, Alicia Corbellini Cryptococcus neoformans Cryptococcus gattii Macrófagos RNA Macrophage Cryptococcus RNAseq mTOR pathway Interatomic networks |
title_short |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
title_full |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
title_fullStr |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
title_full_unstemmed |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
title_sort |
Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells |
author |
Piffer, Alicia Corbellini |
author_facet |
Piffer, Alicia Corbellini Santos, Francine Melise dos Thomé, Marcos Paulo Rosa, Camila Diehl da Garcia, Ane Wichine Acosta Kinskovski, Uriel Perin Schneider, Rafael de Oliveira Gerber, Alexandra Lehmkuhl Feltes, Bruno César Schrank, Augusto Vasconcelos, Ana Tereza Ribeiro de Lenz, Guido Silva, Lívia Kmetzsch Rosa e Vainstein, Marilene Henning Staats, Charley Christian |
author_role |
author |
author2 |
Santos, Francine Melise dos Thomé, Marcos Paulo Rosa, Camila Diehl da Garcia, Ane Wichine Acosta Kinskovski, Uriel Perin Schneider, Rafael de Oliveira Gerber, Alexandra Lehmkuhl Feltes, Bruno César Schrank, Augusto Vasconcelos, Ana Tereza Ribeiro de Lenz, Guido Silva, Lívia Kmetzsch Rosa e Vainstein, Marilene Henning Staats, Charley Christian |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Piffer, Alicia Corbellini Santos, Francine Melise dos Thomé, Marcos Paulo Rosa, Camila Diehl da Garcia, Ane Wichine Acosta Kinskovski, Uriel Perin Schneider, Rafael de Oliveira Gerber, Alexandra Lehmkuhl Feltes, Bruno César Schrank, Augusto Vasconcelos, Ana Tereza Ribeiro de Lenz, Guido Silva, Lívia Kmetzsch Rosa e Vainstein, Marilene Henning Staats, Charley Christian |
dc.subject.por.fl_str_mv |
Cryptococcus neoformans Cryptococcus gattii Macrófagos RNA |
topic |
Cryptococcus neoformans Cryptococcus gattii Macrófagos RNA Macrophage Cryptococcus RNAseq mTOR pathway Interatomic networks |
dc.subject.eng.fl_str_mv |
Macrophage Cryptococcus RNAseq mTOR pathway Interatomic networks |
description |
Cryptococcus neoformans and Cryptococcus gattii are the etiological agents of cryptococcosis, a high mortality disease. The development of such disease depends on the interaction of fungal cells with macrophages, in which they can reside and replicate. In order to dissect the molecular mechanisms by which cryptococcal cells modulate the activity of macrophages, a genome-scale comparative analysis of transcriptional changes in macrophages exposed to Cryptococcus spp. was conducted. Altered expression of nearly 40 genes was detected in macrophages exposed to cryptococcal cells. The major processes were associated with the mTOR pathway, whose associated genes exhibited decreased expression in macrophages incubated with cryptococcal cells. Phosphorylation of p70S6K and GSK-3β was also decreased in macrophages incubated with fungal cells. In this way, Cryptococci presence could drive the modulation of mTOR pathway in macrophages possibly to increase the survival of the pathogen. |
publishDate |
2021 |
dc.date.issued.fl_str_mv |
2021 |
dc.date.accessioned.fl_str_mv |
2023-11-30T03:23:26Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
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info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/267824 |
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1415-4757 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001172711 |
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1415-4757 001172711 |
url |
http://hdl.handle.net/10183/267824 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Genetics and molecular biology. Ribeirão Preto. Vol. 44, no. 3 (2021), e20200390, 13 p. |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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