Literature DB >> 20875859

Altered adult hippocampal neurogenesis in the YAC128 transgenic mouse model of Huntington disease.

Jessica M Simpson1, Joana Gil-Mohapel, Mahmoud A Pouladi, Mohamed Ghilan, Yuanyun Xie, Michael R Hayden, Brian R Christie.   

Abstract

Perturbations in neurogenesis in the adult brain have been implicated in impaired learning and memory. In the present study, we investigated which stages of the neurogenic process are affected in the transgenic YAC128 mouse model of Huntington disease (HD). Hippocampal neuronal proliferation was altered in the dentate gyrus (DG) of YAC128 mice as compared with wild-type (WT) littermate controls in early symptomatic to end-stage mice. In addition, we detected a significantly lower number of immature neurons in the DG of young, pre-symptomatic YAC128 mice. This decrease in neuronal differentiation persisted through the progression of the disease, and resulted in an overall reduction in the number of new mature neurons in the DG of YAC128 mice. There were no changes in cell proliferation and differentiation in the subventricular zone (SVZ). In this study, we demonstrate decreases in neurogenesis in the DG of YAC128 mice, and these deficits may contribute to the cognitive abnormalities observed in these animals. Crown Copyright Â
© 2010. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20875859     DOI: 10.1016/j.nbd.2010.09.012

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  38 in total

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2.  Treatment of depressive-like behaviour in Huntington's disease mice by chronic sertraline and exercise.

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4.  Mutant Ataxin-1 Inhibits Neural Progenitor Cell Proliferation in SCA1.

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5.  HD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity.

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Review 6.  Choosing an animal model for the study of Huntington's disease.

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7.  Mutant Huntingtin promotes autonomous microglia activation via myeloid lineage-determining factors.

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Review 8.  Modeling Huntington's disease with induced pluripotent stem cells.

Authors:  Julia A Kaye; Steven Finkbeiner
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9.  Small-molecule TrkB receptor agonists improve motor function and extend survival in a mouse model of Huntington's disease.

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Journal:  Hum Mol Genet       Date:  2013-02-27       Impact factor: 6.150

10.  Extensive changes in DNA methylation are associated with expression of mutant huntingtin.

Authors:  Christopher W Ng; Ferah Yildirim; Yoon Sing Yap; Simona Dalin; Bryan J Matthews; Patricio J Velez; Adam Labadorf; David E Housman; Ernest Fraenkel
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-22       Impact factor: 11.205

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