Memory deficits of british dementia knock-in mice are prevented by Aβ-precursor protein haploinsufficiency

Robert Tamayev, Luciano D'Adamio

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

Familial British Dementia (FBD) is caused by an autosomal dominant mutation in the BRI2/ITM2B gene (Vidal et al., 1999). FBD KI mice are a model ofFBDthat is genetically congruous to the human disease, because they carry one mutant and one wild-type Bri2/Itm2b allele. Analysis of these mice has shown that the British mutation causes memory impairments due to loss of Bri2 function (Tamayev et al., 2010b). BRI2 is a physiologic inhibitor of processing of the Aβ-precursor protein (APP; Matsuda et al., 2008), a gene associated with Alzheimer's disease (Bertram et al., 2010). Here we show that APP haploinsufficiency prevents memory dysfunctions seen in FBDKI mice. This genetic suppression is consistent with a role for APP in the pathogenesis of memory deficits. Moreover, it provides compelling evidence that the memory dysfunctions caused by the British BRI2 mutant are dependent on endogenous APP and that BRI2 and APP functionally interact. This evidence establishes a mechanistic connection between Familial British and Alzheimer's dementias.

Original languageEnglish (US)
Pages (from-to)5481-5485
Number of pages5
JournalJournal of Neuroscience
Volume32
Issue number16
DOIs
StatePublished - Apr 18 2012

ASJC Scopus subject areas

  • Neuroscience(all)

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