Title
Reduced brain volumes in mice expressing APP-Austrian mutation but not in mice expressing APP-SwedishAustrian mutations Reduced brain volumes in mice expressing APP-Austrian mutation but not in mice expressing APP-SwedishAustrian mutations
Author
Faculty/Department
Faculty of Pharmaceutical, Biomedical and Veterinary Sciences . Biomedical Sciences
Publication type
article
Publication
Amsterdam ,
Subject
Biology
Veterinary medicine
Human medicine
Source (journal)
Neuroscience letters. - Amsterdam
Volume/pages
447(2008) :2/3 , p. 143-147
ISSN
0304-3940
ISI
000261549300010
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Affiliation
University of Antwerp
Abstract
We previously described two transgenic mouse lines expressing sub-endogenous levels of the Austrian APP-T714I mutation (driven by the prenatally active PDGF-â promoter; APP-Au mice) and showing intraneuronal Aâ pathology and reduced brain volumes on MRI at 12 and 20 months of age. To further investigate whether reduced brain sizes were caused by neurodegeneration or a neurodevelopmental defect, we now measured brain volumes as early as postnatal day 10. At this age, a distinguishable reduction in brain volumes was absent, indicating that brain volume deficits in APP-Au mice are not caused by a neurodevelopmental defect. To further study the association between intraneuronal Aâ and reduced brain volumes, we further generated and analyzed an APP transgenic mouse model expressing both Austrian and Swedish (K670N/M671L) mutations (APP-SwAu mice). APP-Swedish mutation is known to lead to altered APP processing in the secretory pathway, precluding its later processing in endosomallysosomal compartments, the site of intraneuronal Aâ accumulation. Also, to have higher levels of transgene expression only after birth, a murine Thy-1 promoter was utilized for APP-SwAu mouse lines. Despite having five times higher transgene APP levels compared to APP-Au mice, APP-SwAu mice showed significantly lower intraneuronal Aâ levels in the absence of reduced brain volumes, suggesting that intraneuronal Aâ accumulation is related to reduced brain volumes in APP-Au mice. These data also provide a first in vivo indication of altered processing of APP-Swedish at sub-endogenous levels, an effect not observed in mouse models expressing the APP-Swedish mutation in high amounts.
E-info
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