Abstract:
To investigate the role of human apolipoprotein E (apoE) on A deposition in vivo, we crossed PDAPP mice lacking mouse Apoe to targeted replacement mice expressing human apoE (PDAPP/TRE2, PDAPP/TRE3, or PDAPP/TRE4). We then measured the levels of apoE protein and A peptides in plasma, CSF, and brain homogenates in these mice at different ages. We also quantified the amount of brain A and amyloid burden in 18-month-old mice. In young PDAPP/TRE4 mice that were analyzed at an age before brain A deposition, we… Show more
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