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Registros recuperados : 2 | |
Registros recuperados : 2 | |
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Registro Completo
Biblioteca(s): |
Embrapa Unidades Centrais. |
Data corrente: |
01/08/2016 |
Data da última atualização: |
01/08/2016 |
Autoria: |
FONSECA, E. T. da; GALINDO, L. T.; PORCIONATTO, M. A.; MIGLINO, M. A. |
Afiliação: |
ERIKA TOLEDO DA FONSECA, UFTT/DC/FMVZ/USP; LAYLA TESTA GALINDO, UNIFESP; MARIMÉLIA A. PORCIONATTO, UNIFESP; MARIA ÁNGELICA MIGLINO, DC/FMVZ/USP. |
Título: |
Culture, characterization and differentiation of neural precursors from the central nervous system of guinea pigs (Cavia porcellus Linnaeus, 1758). |
Ano de publicação: |
2016 |
Fonte/Imprenta: |
Pesquisa Veterinária Brasileira, Brasília, DF, v. 36 (supl. 1), p. 69-78, jun. 2016. |
Idioma: |
Inglês |
Conteúdo: |
Potentially neurogenic areas were initially identified by incorporation of bromodeoxyuridine (BrdU) in cells underlying the subventricular zone (SVZ) of the lateral ventricles wall, hippocampus and olfactory bulbs of newborn guinea pigs. Neural precursors from the SVZ were cultured in suspension, generating neurospheres (NSFs), which, upon dissociation were able to generate new NSFs. Upon culture in the absence of growth factors, cells dissociated from NSFs displayed evidence for neural differentiation, giving rise to cells from neural lineage. Flow cytometry analysis for of NSFs-derived cells after differentiation revealed approximately 13.3% nestin positive, 5.5% Beta-III-tubulin positive, 9% GFAP positive and 7.8% mGalC positive. Functional assays by measurement of calcium influx upon gamma butiric amino acid (GABA) and glutamate stimuli, revealed stimulation in differentiated cells, an indicator of neuronal differentiation. The ability of guinea pig SVZ cells to originate functional neurons in vitro is promising for research and towards a future use of neural stem cells in the therapy of neurological disorders. |
Palavras-Chave: |
Caracterização in vitro; Celula-tronco neural; Cobaio; In vitro characterization; Neural stem cells; Subventricular zone; Zona subventricular. |
Thesagro: |
Produção vegetal. |
Thesaurus NAL: |
Guinea pigs; In vitro culture. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/145947/1/Culture-characterization.pdf
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Marc: |
LEADER 02036naa a2200277 a 4500 001 2049957 005 2016-08-01 008 2016 bl uuuu u00u1 u #d 100 1 $aFONSECA, E. T. da 245 $aCulture, characterization and differentiation of neural precursors from the central nervous system of guinea pigs (Cavia porcellus Linnaeus, 1758). 260 $c2016 520 $aPotentially neurogenic areas were initially identified by incorporation of bromodeoxyuridine (BrdU) in cells underlying the subventricular zone (SVZ) of the lateral ventricles wall, hippocampus and olfactory bulbs of newborn guinea pigs. Neural precursors from the SVZ were cultured in suspension, generating neurospheres (NSFs), which, upon dissociation were able to generate new NSFs. Upon culture in the absence of growth factors, cells dissociated from NSFs displayed evidence for neural differentiation, giving rise to cells from neural lineage. Flow cytometry analysis for of NSFs-derived cells after differentiation revealed approximately 13.3% nestin positive, 5.5% Beta-III-tubulin positive, 9% GFAP positive and 7.8% mGalC positive. Functional assays by measurement of calcium influx upon gamma butiric amino acid (GABA) and glutamate stimuli, revealed stimulation in differentiated cells, an indicator of neuronal differentiation. The ability of guinea pig SVZ cells to originate functional neurons in vitro is promising for research and towards a future use of neural stem cells in the therapy of neurological disorders. 650 $aGuinea pigs 650 $aIn vitro culture 650 $aProdução vegetal 653 $aCaracterização in vitro 653 $aCelula-tronco neural 653 $aCobaio 653 $aIn vitro characterization 653 $aNeural stem cells 653 $aSubventricular zone 653 $aZona subventricular 700 1 $aGALINDO, L. T. 700 1 $aPORCIONATTO, M. A. 700 1 $aMIGLINO, M. A. 773 $tPesquisa Veterinária Brasileira, Brasília, DF$gv. 36 (supl. 1), p. 69-78, jun. 2016.
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Embrapa Unidades Centrais (AI-SEDE) |
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