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1.
Sci Rep ; 6: 28209, 2016 06 17.
Artículo en Inglés | MEDLINE | ID: mdl-27312902

RESUMEN

Whole-brain imaging with light-sheet fluorescence microscopy and optically cleared tissue is a new, rapidly developing research field. Whereas successful attempts to clear and image mouse brain have been reported, a similar result for rats has proven difficult to achieve. Herein, we report on creating novel transgenic rat harboring fluorescent reporter GFP under control of neuronal gene promoter. We then present data on clearing the rat brain, showing that FluoClearBABB was found superior over passive CLARITY and CUBIC methods. Finally, we demonstrate efficient imaging of the rat brain using light-sheet fluorescence microscopy.


Asunto(s)
Mapeo Encefálico/métodos , Encéfalo/diagnóstico por imagen , Imagenología Tridimensional/métodos , Microscopía Fluorescente/métodos , Animales , Proteínas Fluorescentes Verdes/genética , Neuronas/citología , Regiones Promotoras Genéticas/genética , Ratas , Ratas Transgénicas , Ratas Wistar , Antígenos Thy-1/genética , Antígenos Thy-1/metabolismo
2.
Proc Natl Acad Sci U S A ; 109(42): 17093-8, 2012 Oct 16.
Artículo en Inglés | MEDLINE | ID: mdl-23027931

RESUMEN

The memory of fear extinction is context dependent: fear that is suppressed in one context readily renews in another. Understanding of the underlying neuronal circuits is, therefore, of considerable clinical relevance for anxiety disorders. Prefrontal cortical and hippocampal inputs to the amygdala have recently been shown to regulate the retrieval of fear memories, but the cellular organization of these projections remains unclear. By using anterograde tracing in a transgenic rat in which neurons express a dendritically-targeted PSD-95:Venus fusion protein under the control of a c-fos promoter, we found that, during the retrieval of extinction memory, the dominant input to active neurons in the lateral amygdala was from the infralimbic cortex, whereas the retrieval of fear memory was associated with greater hippocampal and prelimbic inputs. This pattern of retrieval-related afferent input was absent in the central nucleus of the amygdala. Our data show functional anatomy of neural circuits regulating fear and extinction, providing a framework for therapeutic manipulations of these circuits.


Asunto(s)
Amígdala del Cerebelo/fisiología , Extinción Psicológica/fisiología , Miedo/fisiología , Sistema Límbico/fisiología , Memoria/fisiología , Vías Nerviosas/anatomía & histología , Proteínas Recombinantes de Fusión/metabolismo , Análisis de Varianza , Animales , Proteínas Bacterianas/metabolismo , Condicionamiento Psicológico , Cartilla de ADN/genética , Homólogo 4 de la Proteína Discs Large , Procesamiento de Imagen Asistido por Computador , Inmunohistoquímica , Péptidos y Proteínas de Señalización Intracelular/genética , Péptidos y Proteínas de Señalización Intracelular/metabolismo , Proteínas Luminiscentes/metabolismo , Masculino , Proteínas de la Membrana/genética , Proteínas de la Membrana/metabolismo , Microscopía Confocal , Vías Nerviosas/fisiología , Ratas , Ratas Transgénicas , Grabación en Video
3.
Genesis ; 47(4): 274-80, 2009 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19241392

RESUMEN

Local and regulated expression of exogenous genes in the central nervous system is one of the major challenges of modern neuroscience. We have approached this issue by applying the inducible tetracycline system to regulate the expression of EGFP reporter gene in double transgenic rats. We have obtained a strong induction of EGFP only in male testes, which correlated with a high level of rtTA expression only in this organ. To overcome the problem of lack of rtTA protein in the transgenic rat brain, we have delivered this Tet system activator with lentiviral vectors into the dentate gyrus of hippocampus of transgenic EGFP rats. As a result, after systemic application of doxycycline we have obtained inducible, stable and restricted to the desired brain region expression of EGFP. An advantage of this strategy is that the transgene is located in the same genetic milieu in every cell of the transgenic organism. This is crucial to obtain uniform expression of the regulated gene within the target brain structure. Combination of rat transgenesis and lentiviral vectors is a novel approach enabling precise spatiotemporal regulation of genes of interest strictly in the brain structure of choice or in other tissues.


Asunto(s)
Encéfalo/metabolismo , Vectores Genéticos/genética , Proteínas Fluorescentes Verdes/metabolismo , Animales , Animales Recién Nacidos , Células Cultivadas , Giro Dentado/metabolismo , Doxiciclina/farmacología , Femenino , Técnica del Anticuerpo Fluorescente , Regulación de la Expresión Génica/efectos de los fármacos , Proteínas Fluorescentes Verdes/genética , Lentivirus/genética , Masculino , Ratas , Ratas Transgénicas , Ratas Wistar , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Elementos de Respuesta/genética , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Tetraciclina/farmacología , Transactivadores/genética , Transactivadores/metabolismo
4.
J Cell Biol ; 180(5): 1021-35, 2008 Mar 10.
Artículo en Inglés | MEDLINE | ID: mdl-18332222

RESUMEN

Temporal lobe epilepsy (TLE) is a devastating disease in which aberrant synaptic plasticity plays a major role. We identify matrix metalloproteinase (MMP) 9 as a novel synaptic enzyme and a key pathogenic factor in two animal models of TLE: kainate-evoked epilepsy and pentylenetetrazole (PTZ) kindling-induced epilepsy. Notably, we show that the sensitivity to PTZ epileptogenesis is decreased in MMP-9 knockout mice but is increased in a novel line of transgenic rats overexpressing MMP-9. Immunoelectron microscopy reveals that MMP-9 associates with hippocampal dendritic spines bearing asymmetrical (excitatory) synapses, where both the MMP-9 protein levels and enzymatic activity become strongly increased upon seizures. Further, we find that MMP-9 deficiency diminishes seizure-evoked pruning of dendritic spines and decreases aberrant synaptogenesis after mossy fiber sprouting. The latter observation provides a possible mechanistic basis for the effect of MMP-9 on epileptogenesis. Our work suggests that a synaptic pool of MMP-9 is critical for the sequence of events that underlie the development of seizures in animal models of TLE.


Asunto(s)
Epilepsia/enzimología , Epilepsia/genética , Hipocampo/anomalías , Metaloproteinasa 9 de la Matriz/genética , Sinapsis/metabolismo , Animales , Animales Modificados Genéticamente , Convulsivantes , Espinas Dendríticas/metabolismo , Espinas Dendríticas/patología , Modelos Animales de Enfermedad , Epilepsia/fisiopatología , Hipocampo/patología , Hipocampo/fisiopatología , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Microscopía Inmunoelectrónica , Fibras Musgosas del Hipocampo/anomalías , Fibras Musgosas del Hipocampo/patología , Fibras Musgosas del Hipocampo/fisiopatología , Vías Nerviosas/anomalías , Vías Nerviosas/patología , Vías Nerviosas/fisiopatología , Plasticidad Neuronal/genética , Técnicas de Cultivo de Órganos , Ratas , Ratas Wistar , Sinapsis/patología
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