The apolipoprotein (APO) E4 isoform is associated with an accelerated rate
of Alzheimer disease (AD) expression in sporadic as well as late-onset fami
lial forms of the disease but the precise mechanism is unknown. In an attem
pt to approach the possible mechanisms involved, APOE receptors have been s
tudied. They all belong to the low density lipoprotein (LDL) receptor famil
y and share the same structural motifs. Some of them are preferentially exp
ressed in the brain such as the LDL receptor related protein, the apolipopr
otein E receptor 2, and the very low density lipoprotein (VLDL) receptor. T
hese receptors have been suspected to be involved in Alzheimer disease at v
arious levels. Among them, the VLDL receptor was extensively explored. Alth
ough genetic studies conducted on a polymorphism in the promoter of the VLD
L receptor in Japanese and Caucasian populations gave divergent results, th
is does not exclude a possible involvement of the VLDL receptor in AD. (C)
2000 Wiley-Liss, Inc.