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1.
J Comp Neurol ; 519(9): 1748-69, 2011 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-21452233

RESUMO

All subdivisions of the adult zebrafish brain maintain niches of constitutive neurogenesis, sustained by quiescent and multipotent progenitor populations. In the telencephalon, the latter potential neural stem cells take the shape of radial glia aligned along the ventricle and are controlled by Notch signalling. With the aim of identifying new markers of this cell type and of comparing the effectors of embryonic and adult neurogenesis, we focused on the family of hairy/enhancer of split [E(spl)] genes. We report the expression of seven hairy/E(spl) (her) genes and the new helt gene in three neurogenic areas of the adult zebrafish brain (telencephalon, hypothalamus, and midbrain) in relation to radial glia, proliferation, and neurogenesis. We show that the expression of most her genes in the adult brain characterizes quiescent radial glia, whereas only few are expressed in progenitor domains engaged in active proliferation or neurogenesis. The low proliferation status of most her-positive progenitors contrasts with the embryonic nervous system, in which her genes are expressed in actively dividing progenitors. Likewise, we demonstrate largely overlapping expression domains of a set of her genes in the adult brain, which is in striking contrast to their distinct embryonic expression profiles. Overall, our data provide a consolidated map of her expression, quiescent glia, proliferation, and neurogenesis in these various subdivisions of the adult brain and suggest distinct regulation and function of Her factors in the embryonic and adult contexts.


Assuntos
Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Encéfalo/metabolismo , Proteínas de Homeodomínio/biossíntese , Neurogênese/fisiologia , Proteínas de Peixe-Zebra/biossíntese , Animais , Fatores de Transcrição Hélice-Alça-Hélice Básicos/biossíntese , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Encéfalo/citologia , Linhagem da Célula/genética , Regulação da Expressão Gênica no Desenvolvimento/fisiologia , Proteínas de Homeodomínio/genética , Proteínas de Homeodomínio/metabolismo , Hipotálamo/citologia , Hipotálamo/metabolismo , Mesencéfalo/citologia , Mesencéfalo/metabolismo , Neuroglia/citologia , Neuroglia/metabolismo , Especificidade da Espécie , Telencéfalo/citologia , Telencéfalo/metabolismo , Fatores de Transcrição HES-1 , Peixe-Zebra , Proteínas de Peixe-Zebra/genética
2.
Development ; 134(5): 845-55, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17251267

RESUMO

Ventral midline Sonic Hedgehog (Shh) signalling is crucial for growth and patterning of the embryonic forebrain. Here, we report how enhanced Shh midline signalling affects the evolution of telencephalic and diencephalic neuronal patterning in the blind cavefish Astyanax mexicanus, a teleost fish closely related to zebrafish. A comparison between cave- and surface-dwelling forms of Astyanax shows that cavefish display larger Shh expression in all anterior midline domains throughout development. This does not affect global forebrain regional patterning, but has several important consequences on specific regions and neuronal populations. First, we show expanded Nkx2.1a expression and higher levels of cell proliferation in the cavefish basal diencephalon and hypothalamus. Second, we uncover an Nkx2.1b-Lhx6-GABA-positive migratory pathway from the subpallium to the olfactory bulb, which is increased in size in cavefish. Finally, we observe heterochrony and enlarged Lhx7 expression in the cavefish basal forebrain. These specific increases in olfactory and hypothalamic forebrain components are Shh-dependent and therefore place the telencephalic midline organisers in a crucial position to modulate forebrain evolution through developmental events, and to generate diversity in forebrain neuronal patterning.


Assuntos
Evolução Biológica , Peixes/embriologia , Proteínas Hedgehog/metabolismo , Prosencéfalo/embriologia , Prosencéfalo/metabolismo , Animais , Padronização Corporal , Movimento Celular , Proliferação de Células , Diencéfalo/embriologia , Diencéfalo/metabolismo , Peixes/metabolismo , Proteínas de Homeodomínio/metabolismo , Hipotálamo/embriologia , Hipotálamo/metabolismo , Neurônios/metabolismo , Bulbo Olfatório/embriologia , Bulbo Olfatório/metabolismo , Especificidade de Órgãos
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