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Data from: overexpression of Dyrk1A is implicated in several cognitive, electrophysiological and neuromorphological alterations found in a mouse model of Down syndrome

Abstract: Down syndrome (DS) phenotypes result from the overexpression of several dosage-sensitive genes. The DYRK1A (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A) gene, which has been implicated in the behavioral and neuronal alterations that are characteristic of DS, plays a role in neuronal progenitor proliferation, neuronal differentiation and long-term potentiation (LTP) mechanisms that contribute to the cognitive deficits found in DS. The purpose of this study was to evaluate the effect of Dyrk1A overexpression on the behavioral and cognitive alterations in the Ts65Dn (TS) mouse model, which is the most commonly utilized mouse model of DS, as well as on several neuromorphological and electrophysiological properties proposed to underlie these deficits. In this study, we analyzed the phenotypic differences in the progeny obtained from crosses of TS females and heterozygous Dyrk1A (+/?) male mice. Our results revealed that normalization of the Dyrk1A copy number in TS mice improved working and reference memory based on the Morris water maze and contextual conditioning based on the fear conditioning test and rescued hippocampal LTP. Concomitant with these functional improvements, normalization of the Dyrk1A expression level in TS mice restored the proliferation and differentiation of hippocampal cells in the adult dentate gyrus (DG) and the density of GABAergic and glutamatergic synapse markers in the molecular layer of the hippocampus. However, normalization of the Dyrk1A gene dosage did not affect other structural (e.g., the density of mature hippocampal granule cells, the DG volume and the subgranular zone area) or behavioral (i.e., hyperactivity/attention) alterations found in the TS mouse. These results suggest that Dyrk1A overexpression is involved in some of the cognitive, electrophysiological and neuromorphological alterations, but not in the structural alterations found in DS, and suggest that pharmacological strategies targeting this gene may improve the treatment of DS-associated learning disabilities.

Data PONE-D-14-18420 This is an excel file containing the data underlying the results described in each manuscript. This file contains 11 spreadsheets, containing the raw data of 1) Dyrk1A protein levels, 2) MWM performance, 3) CFC performance, 4) Rotarod Performance, 5) Open Field performance, 6) LTP results, 7) GAD65/67 and VGLUT levels and VGLUT/GAD65/67 ratio, 8) Ki67, DCX, CLR and DAPI values, 9) DG volume and SGZ ratio, 10) Body weight and 11) Motor tests data

Repositorio: Dryad

 Fecha de publicación: 01/08/2015

 DOI: 10.5061/dryad.p5614

 Citación completa: García-Cerro, S., Martínez, P., Vidal, V., Corrales, A., Flórez, J., Vidal, R., Rueda, N., Arbonés, M., L., Martínez-Cué, C., (2015). Data from: Overexpression of Dyrk1A is implicated in several cognitive, electrophysiological and neuromorphological alterations found in a mouse model of Down syndrome [Dataset]. (Version 1). Dryad. https://doi.org/10.5061/dryad.p5614

Autoría

SUSANA GARCIA CERRO

PAULA MARTINEZ FERNANDEZ

VERONICA VIDAL SANCHEZ

ANDREA CORRALES PARDO

JESUS FLOREZ BELEDO

REBECA VIDAL CASADO

ARBONÉS DE RAFAEL, MARÍA LOURDES