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Neuroscience ; 289: 207-13, 2015 Mar 19.
Artículo en Inglés | MEDLINE | ID: mdl-25573434

RESUMEN

Nuclear hormone receptor coregulator-interacting factor 1 (NIF-1) is a zinc finger nuclear protein that was initially identified to enhance nuclear hormone receptor transcription via its interaction with nuclear hormone receptor coregulator (NRC). NIF-1 may regulate gene transcription either by modulating general transcriptional machinery or remodeling chromatin structure through interactions with specific protein partners. We previously reported that the cytoplasmic/nuclear localization of NIF-1 is regulated by the neuronal Cdk5 activator p35, suggesting potential neuronal functions for NIF-1. The present study reveals that NIF-1 plays critical roles in regulating neuronal morphogenesis at early stages. NIF-1 was prominently expressed in the nuclei of developing rat cortical neurons. Knockdown of NIF-1 expression attenuated both neurite outgrowth in cultured cortical neurons and retinoic acid (RA)-treated Neuro-2a neuroblastoma cells. Furthermore, activity-induced Ca(2+) influx, which is critical for neuronal morphogenesis, stimulated the nuclear localization of NIF-1 in cortical neurons. Suppression of NIF-1 expression reduced the up-regulation of neuronal activity-dependent gene transcription. These findings collectively suggest that NIF-1 directs neuronal morphogenesis during early developmental stages through modulating activity-dependent gene transcription.


Asunto(s)
Péptidos y Proteínas de Señalización Intracelular/metabolismo , Neuritas/fisiología , Proteínas Nucleares/metabolismo , Animales , Calcio/metabolismo , Aumento de la Célula , Línea Celular Tumoral , Núcleo Celular/efectos de los fármacos , Núcleo Celular/metabolismo , Células Cultivadas , Fármacos del Sistema Nervioso Central/farmacología , Corteza Cerebral/citología , Corteza Cerebral/crecimiento & desarrollo , Corteza Cerebral/fisiología , Proteínas de Unión al ADN , Ratones , Neuritas/efectos de los fármacos , Neurogénesis/efectos de los fármacos , Neurogénesis/fisiología , Ratas , Factores de Transcripción , Transcripción Genética/efectos de los fármacos , Transcripción Genética/fisiología , Tretinoina/farmacología
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