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 | Acesso ao texto completo restrito à biblioteca da Embrapa Soja. Para informações adicionais entre em contato com valeria.cardoso@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
30/01/2024 |
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Data da última atualização: |
30/01/2024 |
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Tipo da produção científica: |
Artigo em Anais de Congresso |
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Autoria: |
LAZZAROTTO, J. J.; SCHMITT, R.; ROESSING, A. C. |
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Afiliação: |
JOELSIO JOSE LAZZAROTTO, CNPSO; RICARDO SCHMITT, UNIVERSIDADE ESTADUAL DO CENTRO-OESTE DO PARANÁ; ANTÔNIO CARLOS ROESSING, CNPSO. |
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Título: |
A competitividade da cadeia produtiva da carne bovina da região de Guarapuava, PR. |
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Ano de publicação: |
2005 |
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Fonte/Imprenta: |
In: CONGRESSO DA SOCIEDADE BRASILEIRA DE ECONOMIA E SOCIOLOGIA RURAL, 43., 2005, Ribeirão Preto. Instituições, eficiência, gestão e contratos no sistema agroindustrial: anais. Ribeirão Preto: SOBER, 2005. 1 CD-ROM. |
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Idioma: |
Português |
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Notas: |
Sober 2005. |
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Thesagro: |
Bovino; Cadeia Produtiva. |
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Thesaurus Nal: |
Beef. |
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Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
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Marc: |
LEADER 00687nam a2200169 a 4500
001 2161440
005 2024-01-30
008 2005 bl uuuu u00u1 u #d
100 1 $aLAZZAROTTO, J. J.
245 $aA competitividade da cadeia produtiva da carne bovina da região de Guarapuava, PR.$h[electronic resource]
260 $aIn: CONGRESSO DA SOCIEDADE BRASILEIRA DE ECONOMIA E SOCIOLOGIA RURAL, 43., 2005, Ribeirão Preto. Instituições, eficiência, gestão e contratos no sistema agroindustrial: anais. Ribeirão Preto: SOBER, 2005. 1 CD-ROM.$c2005
500 $aSober 2005.
650 $aBeef
650 $aBovino
650 $aCadeia Produtiva
700 1 $aSCHMITT, R.
700 1 $aROESSING, A. C.
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Embrapa Soja (CNPSO) |
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Biblioteca(s): |
Embrapa Agricultura Digital. |
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Data corrente: |
07/02/2019 |
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Data da última atualização: |
07/02/2019 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
GUIMARÃES, M. Z. P.; DE VECCHI, R.; VITÓRIA, G.; SOCHACKI, J. K.; PAULSEN, B. S.; LIMA, I.; SILVA, F. R. da; COSTA, R. F. M. da; CASTRO, N. G.; BRETON, L.; REHEN, S. K. |
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Afiliação: |
MARÍLIA Z. P. GUIMARÃES, D’Or Institute for Research and Education, UFRJ; RODRIGO DE VECCHI, L’Oréal Research & Innovation, Unicamp; GABRIELA VITÓRIA, L’Oréal Research & Innovation; JAROSLAW K. SOCHACKI, L’Oréal Research & Innovation; BRUNA S. PAULSEN, L’Oréal Research & Innovation; IGOR LIMA, L’Oréal Research & Innovation; FELIPE RODRIGUES DA SILVA, CNPTIA, Unicamp; RODRIGO F. M. DA COSTA, L’Oréal Research & Innovation; NEWTON G. CASTRO, UFRJ; LIONEL BRETON, L’Oréal Research & Innovation; STEVENS K. REHEN, D’Or Institute for Research and Education, UFRJ. |
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Título: |
Generation of iPSC-derived human peripheral sensory neurons releasing substance P elicited by TRPV1 agonists. |
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Ano de publicação: |
2018 |
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Fonte/Imprenta: |
Frontiers in Molecular Neuroscience, v. 11, p. 1-17, Aug. 2018. |
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DOI: |
10.3389/fnmol.2018.00277 |
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Idioma: |
Inglês |
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Notas: |
Article 277. |
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Conteúdo: |
Neural crest stem cells (NCPCs) have been shown to differentiate into various cell types and tissues during embryonic development, including sensory neurons. The few studies addressing the generation of NCPCs and peripheral sensory neurons (PSNs) from human induced pluripotent stem cells (hiPSCs), generated sensory cells without displaying robust activity. Here, we describe an efficient strategy for hiPSCs differentiation into NCPCs and functional PSNs using chemically defined media and factors to achieve efficient differentiation, confirmed by the expression of specific markers. After 10 days hiPSCs differentiated into NCPCs, cells were then maintained in neural induction medium containing defined growth factors for PSNs differentiation, followed by 10 days in neonatal human epidermal keratinocytes- (HEKn-) conditioned medium (CM). We observed a further increase in PSN markers expression and neurites length after CM treatment. The resulting neurons elicited action potentials after current injection and released substance P (SP) in response to nociceptive agents such as anandamide and resiniferatoxin. Anandamide induced substance P release via activation of TRPV1 and not CB1. Transcriptomic analysis of the PSNs revealed the main dorsal root ganglia neuronal markers and a transcriptional profile compatible with C fiber-low threshold mechanoreceptors. TRPV1 was detected by immunofluorescence and RNA-Seq in multiple experiments. In conclusion, the developed strategy generated PSNs useful for drug screening that could be applied to patient-derived hiPSCs, consisting in a powerful tool to model human diseases in vitro. MenosNeural crest stem cells (NCPCs) have been shown to differentiate into various cell types and tissues during embryonic development, including sensory neurons. The few studies addressing the generation of NCPCs and peripheral sensory neurons (PSNs) from human induced pluripotent stem cells (hiPSCs), generated sensory cells without displaying robust activity. Here, we describe an efficient strategy for hiPSCs differentiation into NCPCs and functional PSNs using chemically defined media and factors to achieve efficient differentiation, confirmed by the expression of specific markers. After 10 days hiPSCs differentiated into NCPCs, cells were then maintained in neural induction medium containing defined growth factors for PSNs differentiation, followed by 10 days in neonatal human epidermal keratinocytes- (HEKn-) conditioned medium (CM). We observed a further increase in PSN markers expression and neurites length after CM treatment. The resulting neurons elicited action potentials after current injection and released substance P (SP) in response to nociceptive agents such as anandamide and resiniferatoxin. Anandamide induced substance P release via activation of TRPV1 and not CB1. Transcriptomic analysis of the PSNs revealed the main dorsal root ganglia neuronal markers and a transcriptional profile compatible with C fiber-low threshold mechanoreceptors. TRPV1 was detected by immunofluorescence and RNA-Seq in multiple experiments. In conclusion, the developed strategy generated P... Mostrar Tudo |
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Palavras-Chave: |
Human induced pluripotent stem cells; Neural crest stem cells; Neurônios sensoriais; Pré-clínico; Substância P; TRPV1. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/192302/1/AP-Generation-iPSC-Felipe.pdf
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Marc: |
LEADER 02655naa a2200337 a 4500
001 2105696
005 2019-02-07
008 2018 bl uuuu u00u1 u #d
024 7 $a10.3389/fnmol.2018.00277$2DOI
100 1 $aGUIMARÃES, M. Z. P.
245 $aGeneration of iPSC-derived human peripheral sensory neurons releasing substance P elicited by TRPV1 agonists.$h[electronic resource]
260 $c2018
500 $aArticle 277.
520 $aNeural crest stem cells (NCPCs) have been shown to differentiate into various cell types and tissues during embryonic development, including sensory neurons. The few studies addressing the generation of NCPCs and peripheral sensory neurons (PSNs) from human induced pluripotent stem cells (hiPSCs), generated sensory cells without displaying robust activity. Here, we describe an efficient strategy for hiPSCs differentiation into NCPCs and functional PSNs using chemically defined media and factors to achieve efficient differentiation, confirmed by the expression of specific markers. After 10 days hiPSCs differentiated into NCPCs, cells were then maintained in neural induction medium containing defined growth factors for PSNs differentiation, followed by 10 days in neonatal human epidermal keratinocytes- (HEKn-) conditioned medium (CM). We observed a further increase in PSN markers expression and neurites length after CM treatment. The resulting neurons elicited action potentials after current injection and released substance P (SP) in response to nociceptive agents such as anandamide and resiniferatoxin. Anandamide induced substance P release via activation of TRPV1 and not CB1. Transcriptomic analysis of the PSNs revealed the main dorsal root ganglia neuronal markers and a transcriptional profile compatible with C fiber-low threshold mechanoreceptors. TRPV1 was detected by immunofluorescence and RNA-Seq in multiple experiments. In conclusion, the developed strategy generated PSNs useful for drug screening that could be applied to patient-derived hiPSCs, consisting in a powerful tool to model human diseases in vitro.
653 $aHuman induced pluripotent stem cells
653 $aNeural crest stem cells
653 $aNeurônios sensoriais
653 $aPré-clínico
653 $aSubstância P
653 $aTRPV1
700 1 $aDE VECCHI, R.
700 1 $aVITÓRIA, G.
700 1 $aSOCHACKI, J. K.
700 1 $aPAULSEN, B. S.
700 1 $aLIMA, I.
700 1 $aSILVA, F. R. da
700 1 $aCOSTA, R. F. M. da
700 1 $aCASTRO, N. G.
700 1 $aBRETON, L.
700 1 $aREHEN, S. K.
773 $tFrontiers in Molecular Neuroscience$gv. 11, p. 1-17, Aug. 2018.
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