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Registro Completo |
Biblioteca(s): |
Embrapa Amazônia Oriental. |
Data corrente: |
29/11/1999 |
Data da última atualização: |
05/02/2021 |
Autoria: |
LAMEIRA, O. A.; COSTA, M. P. da; PINTO, J. E. B. P.; GAVILANES, M. L. |
Afiliação: |
OSMAR ALVES LAMEIRA, CPATU. |
Título: |
Tissue culture propagation of Cephaelis ipecacuanha A. Richard: effect of growth regulators on plantlet root formation. |
Ano de publicação: |
1997 |
Fonte/Imprenta: |
Ciência e Agrotecnologia, Lavras, v. 21, n. 3, p. 390-392, jul./set. 1997. |
Idioma: |
Inglês |
Palavras-Chave: |
Drug plants; Ipeca. |
Thesagro: |
Cephaelis Ipecacuanha; Cultura de Tecido; Planta Medicinal; Regulador de Crescimento. |
Thesaurus Nal: |
plant growth substances; tissue culture. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/220942/1/Tissue-culture-propagation.pdf
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Marc: |
LEADER 00769naa a2200241 a 4500 001 1398488 005 2021-02-05 008 1997 bl uuuu u00u1 u #d 100 1 $aLAMEIRA, O. A. 245 $aTissue culture propagation of Cephaelis ipecacuanha A. Richard$beffect of growth regulators on plantlet root formation. 260 $c1997 650 $aplant growth substances 650 $atissue culture 650 $aCephaelis Ipecacuanha 650 $aCultura de Tecido 650 $aPlanta Medicinal 650 $aRegulador de Crescimento 653 $aDrug plants 653 $aIpeca 700 1 $aCOSTA, M. P. da 700 1 $aPINTO, J. E. B. P. 700 1 $aGAVILANES, M. L. 773 $tCiência e Agrotecnologia, Lavras$gv. 21, n. 3, p. 390-392, jul./set. 1997.
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Embrapa Amazônia Oriental (CPATU) |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Gado de Leite. Para informações adicionais entre em contato com cnpgl.biblioteca@embrapa.br. |
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 |
Circulação/Nível: |
A - 2 |
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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