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Human APOE allelic variants suppress the formation of diffuse and fibrillar Aβ deposits relative to mouse Apoe in transgenic mouse models of Alzheimer amyloidosis

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By Guilian Xu, Parul Bali, Patricia Sacilotto, Carmelina Gorski
| biorxiv.org
Abstract Background: Apolipoprotein E (apoE) modulates the deposition of amyloid β (Aβ) aggregates in Alzheimers disease (AD) in an isoform-dependent manner. In transgenic mouse models of AD-amyloidosis, replacing mouse Apoe alleles with human APOE variants suppresses fibrillar Aβ deposits. In the PD-APP transgenic mouse model, deletion of the Apoe gene led to selective reduction of fibrillar deposits with increased diffuse deposits.
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