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Registro Completo |
Biblioteca(s): |
Embrapa Gado de Leite. |
Data corrente: |
16/01/2014 |
Data da última atualização: |
09/02/2024 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
RODRIGUES, M. F.; ALVES, C. C. S.; FIGUEIREDO, B. B. M.; REZENDE, A. B.; WOHLRES-VIANA, S.; SILVA, V. L.; MACHADO, M. A.; TEIXEIRA, H. C. |
Afiliação: |
MICHELE F. RODRIGUES, UFJF; CAIO C. S. ALVES, UFJF; BÁRBARA B. M. FIGUEIREDO, UFJF; ALICE B. REZENDE, UFJF; SABINE WOHLRES-VIANA, UFJF; VANIA LUCIA DA SILVA, UFJF; MARCO ANTONIO MACHADO, CNPGL; HENRIQUE C. TEIXEIRA, UFJF. |
Título: |
Tumour necrosis factor receptors and apoptosis of alveolar macrophages during early infection with attenuaed and virulent Mycobacterium bovis. |
Ano de publicação: |
2013 |
Fonte/Imprenta: |
Immunology, v. 139, n. 4, p. 503-512, 2013. |
DOI: |
https://doi.org/10.1111%2Fimm.12097 |
Idioma: |
Inglês |
Conteúdo: |
Apoptosis of macrophages has been reported as an effective host strategy to control the growth of intracellular pathogens, including pathogenic mycobacteria. Tumour necrosis factor-α (TNF-α) plays an important role in the modulation of apoptosis of infected macrophages. It exerts its biological activities via two distinct cell surface receptors, TNFR1 and TNFR2, whose extracellular domain can be released by proteolysis forming soluble TNF receptors (sTNFR1 and sTNFR2). The signalling through TNFR1 initiates the majority of the biological functions of TNF-α, leading to either cell death or survival whereas TNFR2 mediates primarily survival signals. Here, the expression of TNF-α receptors and the apoptosis of alveolar macrophages were investigated during the early phase of infection with attenuated and virulent mycobacteria in mice. A significant increase of apoptosis and high expression of TNFR1 were observed in alveolar macrophages at 3 and 7 days after infection with attenuated Mycobacterium bovis but only on day 7 in infection with the virulent M. bovis. Low surface expression of TNFR1 and increased levels of sTNFR1 on day 3 after infection by the virulent strain were associated with reduced rates of apoptotic macrophages. In addition, a significant reduction in apoptosis of alveolar macrophages was observed in TNFR1−/− mice at day 3 after bacillus Calmette–Guérin infection. These results suggest a potential role for TNFR1 in mycobacteria-induced alveolar macrophage apoptosis in vivo. In this scenario, shedding of TNFR1 seems to contribute to the modulation of macrophage apoptosis in a strain-dependent manner. MenosApoptosis of macrophages has been reported as an effective host strategy to control the growth of intracellular pathogens, including pathogenic mycobacteria. Tumour necrosis factor-α (TNF-α) plays an important role in the modulation of apoptosis of infected macrophages. It exerts its biological activities via two distinct cell surface receptors, TNFR1 and TNFR2, whose extracellular domain can be released by proteolysis forming soluble TNF receptors (sTNFR1 and sTNFR2). The signalling through TNFR1 initiates the majority of the biological functions of TNF-α, leading to either cell death or survival whereas TNFR2 mediates primarily survival signals. Here, the expression of TNF-α receptors and the apoptosis of alveolar macrophages were investigated during the early phase of infection with attenuated and virulent mycobacteria in mice. A significant increase of apoptosis and high expression of TNFR1 were observed in alveolar macrophages at 3 and 7 days after infection with attenuated Mycobacterium bovis but only on day 7 in infection with the virulent M. bovis. Low surface expression of TNFR1 and increased levels of sTNFR1 on day 3 after infection by the virulent strain were associated with reduced rates of apoptotic macrophages. In addition, a significant reduction in apoptosis of alveolar macrophages was observed in TNFR1−/− mice at day 3 after bacillus Calmette–Guérin infection. These results suggest a potential role for TNFR1 in mycobacteria-induced alveolar macrophage apopto... Mostrar Tudo |
Palavras-Chave: |
Apoptose; Macrófagos; Receptor do fator de necrose tumoral. |
Thesagro: |
Mycobacterium Bovis. |
Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
Marc: |
LEADER 02510naa a2200265 a 4500 001 1976421 005 2024-02-09 008 2013 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1111%2Fimm.12097$2DOI 100 1 $aRODRIGUES, M. F. 245 $aTumour necrosis factor receptors and apoptosis of alveolar macrophages during early infection with attenuaed and virulent Mycobacterium bovis.$h[electronic resource] 260 $c2013 520 $aApoptosis of macrophages has been reported as an effective host strategy to control the growth of intracellular pathogens, including pathogenic mycobacteria. Tumour necrosis factor-α (TNF-α) plays an important role in the modulation of apoptosis of infected macrophages. It exerts its biological activities via two distinct cell surface receptors, TNFR1 and TNFR2, whose extracellular domain can be released by proteolysis forming soluble TNF receptors (sTNFR1 and sTNFR2). The signalling through TNFR1 initiates the majority of the biological functions of TNF-α, leading to either cell death or survival whereas TNFR2 mediates primarily survival signals. Here, the expression of TNF-α receptors and the apoptosis of alveolar macrophages were investigated during the early phase of infection with attenuated and virulent mycobacteria in mice. A significant increase of apoptosis and high expression of TNFR1 were observed in alveolar macrophages at 3 and 7 days after infection with attenuated Mycobacterium bovis but only on day 7 in infection with the virulent M. bovis. Low surface expression of TNFR1 and increased levels of sTNFR1 on day 3 after infection by the virulent strain were associated with reduced rates of apoptotic macrophages. In addition, a significant reduction in apoptosis of alveolar macrophages was observed in TNFR1−/− mice at day 3 after bacillus Calmette–Guérin infection. These results suggest a potential role for TNFR1 in mycobacteria-induced alveolar macrophage apoptosis in vivo. In this scenario, shedding of TNFR1 seems to contribute to the modulation of macrophage apoptosis in a strain-dependent manner. 650 $aMycobacterium Bovis 653 $aApoptose 653 $aMacrófagos 653 $aReceptor do fator de necrose tumoral 700 1 $aALVES, C. C. S. 700 1 $aFIGUEIREDO, B. B. M. 700 1 $aREZENDE, A. B. 700 1 $aWOHLRES-VIANA, S. 700 1 $aSILVA, V. L. 700 1 $aMACHADO, M. A. 700 1 $aTEIXEIRA, H. C. 773 $tImmunology$gv. 139, n. 4, p. 503-512, 2013.
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Embrapa Gado de Leite (CNPGL) |
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Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
Data corrente: |
06/12/2007 |
Data da última atualização: |
10/07/2008 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Circulação/Nível: |
-- - -- |
Autoria: |
MELATTI, V.; PRAÇA, L. B.; SUJII, E.; MONNERAT, R. G. |
Título: |
Metodologia de bioensaio de Bacillus thuringiensis contra o pulgão do algodoeiro (Aphis gossypii). |
Ano de publicação: |
2006 |
Fonte/Imprenta: |
In: ENCONTRO DO TALENTO ESTUDANTIL DA EMBRAPA RECURSOS GENÉTICOS E BIOTECNOLOGIA, 11., 2006, Brasília, DF. Anais: resumos dos trabalhos. Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 2006. |
Páginas: |
p. 146. |
Idioma: |
Português |
Palavras-Chave: |
Bioensaio; Pulgão do algodoeiro. |
Thesagro: |
Aphis Gossypii; Bacillus Thuringiensis; Controle Biológico. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/CENARGEN/28440/1/tales2006.pdf
https://www.cenargen.embrapa.br/publica/talento/tales2006.pdf
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Marc: |
LEADER 00768nam a2200205 a 4500 001 1188611 005 2008-07-10 008 2006 bl uuuu u00u1 u #d 100 1 $aMELATTI, V. 245 $aMetodologia de bioensaio de Bacillus thuringiensis contra o pulgão do algodoeiro (Aphis gossypii). 260 $aIn: ENCONTRO DO TALENTO ESTUDANTIL DA EMBRAPA RECURSOS GENÉTICOS E BIOTECNOLOGIA, 11., 2006, Brasília, DF. Anais: resumos dos trabalhos. Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia$c2006 300 $ap. 146. 650 $aAphis Gossypii 650 $aBacillus Thuringiensis 650 $aControle Biológico 653 $aBioensaio 653 $aPulgão do algodoeiro 700 1 $aPRAÇA, L. B. 700 1 $aSUJII, E. 700 1 $aMONNERAT, R. G.
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