Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
Gene Expr Patterns ; 21(1): 41-53, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-27364471

RESUMO

Krüpple-like factors (KLFs) are transcription factors with zinc finger DNA binding domains known to play important roles in brain development and central nervous system (CNS) regeneration. There is little information on KLFs expression in adult vertebrate CNS. In this study, we used in situ hybridization to examine Klf7 mRNA (klf7) and Klf6a mRNA (klf6a) expression in adult zebrafish CNS. Both klfs exhibit wide and similar expression in the zebrafish CNS. Brain areas containing strongly labeled cells include the ventricular regions of the dorsomedial telencephalon, the ventromedial telencephalon, periventricular regions of the thalamus and hypothalamus, torus longitudinalis, stratum periventriculare of the optic tectum, granular regions of the cerebellar body and valvula, and superficial layers of the facial and vagal lobes. In the spinal cord, klf7- and klf6a-expressing cells are found in both the dorsal and ventral horns. Numerous sensory structures (e.g. auditory, lateral line, olfactory and visual) and several motor nuclei (e.g. oculomotor, trigeminal, and vagal motor nuclei) contain klf7- and/or klf6a-expressing cells. Our results may provide useful information for determining these Klfs in maintenance and/or function in adult CNS.


Assuntos
Sistema Nervoso Central/metabolismo , Proteínas do Tecido Nervoso/biossíntese , Medula Espinal/metabolismo , Proteínas de Peixe-Zebra/biossíntese , Peixe-Zebra/genética , Animais , Encéfalo/metabolismo , Cerebelo/metabolismo , Regulação da Expressão Gênica/genética , Hibridização In Situ , Proteínas do Tecido Nervoso/genética , Neurônios/metabolismo , RNA Mensageiro/biossíntese , Telencéfalo/metabolismo , Tálamo/metabolismo , Proteínas de Peixe-Zebra/genética
2.
J Mol Endocrinol ; 52(3): T29-42, 2014 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-24868105

RESUMO

The melanocortin receptors (MCRs) are a family of G protein-coupled receptors that are activated by melanocortin ligands derived from the proprotein, proopiomelanocortin (POMC). During the radiation of the gnathostomes, the five receptors have become functionally segregated (i.e. melanocortin 1 receptor (MC1R), pigmentation regulation; MC2R, glucocorticoid synthesis; MC3R and MC4R, energy homeostasis; and MC5R, exocrine gland physiology). A focus of this review is the role that ligand selectivity plays in the hypothalamus/pituitary/adrenal-interrenal (HPA-I) axis of teleosts and tetrapods as a result of the exclusive ligand selectivity of MC2R for the ligand ACTH. A second focal point of this review is the roles that the accessory proteins melanocortin 2 receptor accessory protein 1 (MRAP1) and MRAP2 are playing in, respectively, the HPA-I axis (MC2R) and the regulation of energy homeostasis by neurons in the hypothalamus (MC4R) of teleosts and tetrapods. In addition, observations are presented on trends in the ligand selectivity parameters of cartilaginous fish, teleost, and tetrapod MC1R, MC3R, MC4R, and MC5R paralogs, and the modeling of the HFRW motif of ACTH(1-24) when compared with α-MSH. The radiation of the MCRs during the evolution of the gnathostomes provides examples of how the physiology of endocrine and neuronal circuits can be shaped by ligand selectivity, the intersession of reverse agonists (agouti-related peptides (AGRPs)), and interactions with accessory proteins (MRAPs).


Assuntos
Evolução Molecular , Peixes/genética , Melanocortinas/genética , Receptores de Melanocortina/genética , Glândulas Suprarrenais/fisiologia , Hormônio Adrenocorticotrópico/metabolismo , Sequência de Aminoácidos , Animais , Evolução Biológica , Metabolismo Energético , Glândulas Exócrinas/fisiologia , Peixes/metabolismo , Glucocorticoides/biossíntese , Hipotálamo/fisiologia , Neurônios/metabolismo , Pigmentação/fisiologia , Hipófise/fisiologia , Pró-Opiomelanocortina/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA