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Neurotrophin receptor p75(NTR) mediates Huntington's disease-associated synaptic and memory dysfunction.


ABSTRACT: Learning and memory deficits are early clinical manifestations of Huntington's disease (HD). These cognitive impairments have been mainly associated with frontostriatal HD pathology; however, compelling evidence provided by several HD murine models suggests that the hippocampus may contribute to synaptic deficits and memory dysfunction in HD. The neurotrophin receptor p75(NTR) negatively regulates spine density, which is associated with learning and memory; therefore, we explored whether disturbed p75(NTR) function in the hippocampus could contribute to synaptic dysfunction and memory deficits in HD. Here, we determined that levels of p75(NTR) are markedly increased in the hippocampus of 2 distinct mouse models of HD and in HD patients. Normalization of p75(NTR) levels in HD mutant mice he

SUBMITTER: Brito V 

PROVIDER: S-EPMC4191006 | biostudies-literature | 2014 Oct

REPOSITORIES: biostudies-literature

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