Transcriptomic analysis reveals that mTOR pathway can be modulated in macrophage cells by the presence of cryptococcal cells

Detalhes bibliográficos
Autor(a) principal: Piffer, Alicia Corbellini
Data de Publicação: 2021
Outros Autores: 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
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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spelling 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
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/267824
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dc.language.iso.fl_str_mv eng
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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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