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1.
Blood ; 118(5): 1374-85, 2011 Aug 04.
Artículo en Inglés | MEDLINE | ID: mdl-21628412

RESUMEN

c-Maf is one of the large Maf (musculoaponeurotic fibrosarcoma) transcription factors that belong to the activated protein-1 super family of basic leucine zipper proteins. Despite its overexpression in hematologic malignancies, the physiologic roles c-Maf plays in normal hematopoiesis have been largely unexplored. On a C57BL/6J background, c-Maf(-/-) embryos succumbed from severe erythropenia between embryonic day (E) 15 and E18. Flow cytometric analysis of fetal liver cells showed that the mature erythroid compartments were significantly reduced in c-Maf(-/-) embryos compared with c-Maf(+/+) littermates. Interestingly, the CFU assay indicated there was no significant difference between c-Maf(+/+) and c-Maf(-/-) fetal liver cells in erythroid colony counts. This result indicated that impaired definitive erythropoiesis in c-Maf(-/-) embryos is because of a non-cell-autonomous effect, suggesting a defective erythropoietic microenvironment in the fetal liver. As expected, the number of erythroblasts surrounding the macrophages in erythroblastic islands was significantly reduced in c-Maf(-/-) embryos. Moreover, decreased expression of VCAM-1 was observed in c-Maf(-/-) fetal liver macrophages. In conclusion, these results strongly suggest that c-Maf is crucial for definitive erythropoiesis in fetal liver, playing an important role in macrophages that constitute erythroblastic islands.


Asunto(s)
Eritroblastos/citología , Eritroblastos/fisiología , Eritropoyesis/genética , Feto/citología , Hígado/citología , Proteínas Proto-Oncogénicas c-maf/fisiología , Animales , Comunicación Celular/genética , Movimiento Celular/genética , Proliferación Celular , Embrión de Mamíferos , Eritroblastos/metabolismo , Feto/metabolismo , Perfilación de la Expresión Génica , Hígado/embriología , Hígado/metabolismo , Macrófagos/metabolismo , Macrófagos/fisiología , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Análisis por Micromatrices , Proteínas Proto-Oncogénicas c-maf/genética
2.
Dent Mater J ; 36(3): 309-318, 2017 May 31.
Artículo en Inglés | MEDLINE | ID: mdl-28154315

RESUMEN

The purpose of this study was to investigate methods for evaluating objectively the removability of three commercially available home reliners (Cushion Correct, Tafugurippu Pink A and Liodent Pink). After immersing each of the reliners in distilled water at 37ºC for 24 h, we compared their removability using the peel test with a finger, which was evaluated based on a visual analogue scale and the percentage of the residual area. An experimental rake-up test was also undertaken to quantify removability, evaluated based on the total amount of work required to remove it. The Tafugurippu Pink A product was easier to remove with a finger than the other two home reliner products, and required the least total amount of work to be removed in the experimental rake-up test. Furthermore, the rake-up test performed could possibly be used for objective evaluation of the removability of home reliner.


Asunto(s)
Alineadores Dentales , Ensayo de Materiales , Agua
3.
Gene ; 445(1-2): 66-72, 2009 Sep 15.
Artículo en Inglés | MEDLINE | ID: mdl-19539733

RESUMEN

c-Maf, which is one of the large Maf transcription factors, can bind to Maf recognition element (MARE) and activates transcription of target genes. Although c-Maf is expressed in macrophages and directly regulates the expression of interleukin-10, detailed information regarding its function in the null mutant phenotype of tissue macrophages remain unknown. In this study, we demonstrated that c-Maf is specifically expressed in the F4/80 positive fetal liver and adult macrophages. The expression of F4/80, which is a tissue macrophage-specific seven trans-membrane receptor, was dramatically suppressed in the c-Maf-deficient macrophage, whereas the expression of Mac-1 was not affected, suggesting that c-Maf is not necessary for the lineage commitment of macrophages. Luciferase reporter and EMSA showed that c-Maf directly regulates the expression of F4/80 by interacting with the half-MARE site of the F4/80 promoter. These results suggest that c-Maf is required for the F4/80 expression in macrophages in vivo.


Asunto(s)
Antígenos de Diferenciación/genética , Macrófagos/metabolismo , Proteínas Proto-Oncogénicas c-maf/fisiología , Animales , Antígenos de Diferenciación/metabolismo , Secuencia de Bases , Células Cultivadas , Embrión de Mamíferos , Regulación de la Expresión Génica , Hígado/embriología , Hígado/metabolismo , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Datos de Secuencia Molecular , Proteínas Proto-Oncogénicas c-maf/genética , Proteínas Proto-Oncogénicas c-maf/metabolismo , Homología de Secuencia de Ácido Nucleico
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