Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Calcif Tissue Int ; 100(3): 311-322, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-28012106

RESUMO

The transcription factor c-MYB is a well-known marker of undifferentiated cells such as haematopoietic cell precursors, but recently it has also been observed in differentiated cells that produce hard tissues. Our previous findings showed the presence of c-MYB in intramembranous bones and its involvement in the chondrogenic steps of endochondral ossification, where the up-regulation of early chondrogenic markers after c-myb overexpression was observed. Since we previously detected c-MYB in osteoblasts, we aimed to analyse the localisation of c-MYB during later stages of endochondral bone formation and address its function during bone matrix production. c-MYB-positive cells were found in the chondro-osseous junction zone in osteoblasts of trabecular bone as well as deeper in the zone of ossification in cells of spongy bone. To experimentally evaluate the osteogenic potential of c-MYB during endochondral bone formation, micromasses derived from embryonic mouse limb buds were established. Nuclear c-MYB protein expression was observed in long-term micromasses, especially in the areas around nodules. c-myb overexpression induced the expression of osteogenic-related genes such as Bmp2, Comp, Csf2 and Itgb1. Moreover, alizarin red staining and osteocalcin labelling promoted mineralised matrix production in c-myb-overexpressing cultures, whereas downregulation of c-myb by siRNA reduced mineralised matrix production. In conclusion, c-Myb plays a role in the osteogenesis of long bones by inducing osteogenic genes and causing the enhancement of mineral matrix production. This action of the transcription factor c-Myb might be of interest in the future for the establishment of novel approaches to tissue regeneration.


Assuntos
Osso e Ossos/metabolismo , Osteoblastos/metabolismo , Osteogênese/fisiologia , Proteínas Proto-Oncogênicas c-myb/metabolismo , Animais , Diferenciação Celular/fisiologia , Condrogênese/fisiologia , Camundongos , Osteoblastos/citologia , Osteocalcina/metabolismo , Proteínas Proto-Oncogênicas c-myb/genética , Regulação para Cima
2.
Development ; 125(9): 1759-68, 1998 May.
Artigo em Inglês | MEDLINE | ID: mdl-9521913

RESUMO

decapentaplegic (dpp) is a Transforming Growth Factor beta (TGF-beta)-related growth factor that controls multiple developmental processes in Drosophila. To identify components involved in dpp signaling, we carried out a genetic screen for dominant enhancer mutations of a hypomorphic allele of thick veins (tkv), a type I receptor for dpp. We recovered new alleles of tkv, punt, Mothers against dpp (Mad) and Medea (Med), all of which are known to mediate dpp signaling. We also recovered mutations in the 60A gene which encodes another TGF-beta-related factor in Drosophila. DNA sequence analysis established that all three 60A alleles were nonsense mutations in the prodomain of the 60A polypeptide. These mutations in 60A caused defects in midgut morphogenesis and fat body differentiation. We present evidence that when dpp signaling is compromised, lowering the level of 60A impairs several dpp-dependent developmental processes examined, including the patterning of the visceral mesoderm, the embryonic ectoderm and the imaginal discs. These results provide the first in vivo evidence for the involvement of 60A in the dpp pathway. We propose that 60A activity is required to maintain optimal signaling capacity of the dpp pathway, possibly by forming biologically active heterodimers with Dpp proteins.


Assuntos
Proteínas de Drosophila , Drosophila/genética , Proteínas de Insetos/fisiologia , Mutação/genética , Proteínas Repressoras , Transdução de Sinais/genética , Fator de Crescimento Transformador beta/genética , Receptores de Ativinas , Animais , Proteína Morfogenética Óssea 7 , Proteínas Morfogenéticas Ósseas , Análise Mutacional de DNA , Proteínas de Ligação a DNA/genética , Teste de Complementação Genética , Proteínas de Insetos/genética , Mesoderma , Fenótipo , Proteínas Serina-Treonina Quinases/genética , Receptores de Superfície Celular/genética , Receptores de Fatores de Crescimento/genética , Proteína Smad4 , Transativadores/genética , Fatores de Transcrição/genética
3.
Appl Opt ; 33(2): 258-66, 1994 Jan 10.
Artigo em Inglês | MEDLINE | ID: mdl-20862015

RESUMO

Optically addressed ferroelectric liquid-crystal devices present certain characteristics that make them attractive for all-optical implementations of neural architectures. This is particularly true for the implementation of analog self-organizing systems such as Kohonen's self-organizing map. The optical architecture proposed here is based on the principle of a resonator memory. The main novelty lies in the two-dimensional, continuous, binary information encoding and organization. Basic operations such as neural decision, weight updating, and information spatial ordering are investigated. The principle of a learning procedure close to the Hebbian rule is discussed.

4.
Appl Opt ; 31(20): 3930-6, 1992 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-20725369

RESUMO

We report the characteristics of a truly bistable optically addressed ferroelectric liquid-crystal spatial light modulator that is capable of storing binary images. We show that, in addition to this bistability, a nonlinear response and gray scales can be observed under certain operating conditions. We then report on how these capabilities can be used in implementing optical neurocomputing architectures.

5.
Diamond ; 1(1): 18-9, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1802307
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...