An increased prevalence of apolipoprotein E (ApoE) epsilon4 allele exi
sts in late onset familial Alzheimer's disease. We found, in sporadic
Alzheimer's disease, that 62% of patients possessed an ApoE-epsilon4 a
llele, compared with 20% of controls. ApoE-epsilon4/4 patients had mor
e senile plaques (SPs) than epsilon3/3 patients. ApoE immunoreactivity
of SPs was equivalent in both groups. Two receptors bind ApoE complex
es, the low density lipoprotein (LDL) receptor and the LDL receptor-re
lated protein (LRP). In normal brain, anti-LRP antibodies strongly sta
ined neurons and lightly stained astrocytes; anti-LDL receptor antibod
ies stained only the neuropil and astrocytes. In Alzheimer's disease,
SPs and reactive astrocytes were also strongly LRP immunoreactive. Col
ocalization of ApoE and LRP to SPs implies that these molecules may be
involved in metabolism of components of SPs.