From: Soluble apoE/Aβ complex: mechanism and therapeutic target for APOE4-induced AD risk
Study | Biological source | Detection method | Results |
---|---|---|---|
Naslund et al, 1995 [36] | Human brain (AD & NAD) | SDS-PAGE (Non-reducing), WB | AD > NAD, No apoE isoform differences measured |
Russo et al, 1998 [46] | Human brain (AD & NAD) | IP, SDS-PAGE (Non-reducing?), WB | NAD apoE23/Aβ = NAD apoE33/Aβ = NAD apoE34/Aβ >> |
AD apoE33/Aβ > AD apoE44/Aβ | |||
SDS & protease digestion stability: NAD > AD | |||
Yamauchi et al, 1999 [48] | Human CSF & serum (NAD) | SDS-PAGE (Non-reducing), WB | apoE33/Aβ > apoE44/Aβ (ND) |
Hashimoto et al, 2012 [27] | Human brain (NAD) | SEC, SDS-PAGE (Reducing), WB | No complex measured, HMW Aβ interacts with apoE on HDL particles |
LaDu et al, 2012 [63] | Human plasma (NAD) | SEC, SDS-PAGE (Non-reducing), WB | 95% Aβ elutes with lipoproteins |
Human CSF (NAD) | 100% Aβ associated with apoE containing lipoproteins, apoE monomer/Aβ (45 kDa) & apoE dimer/Aβ (97 kDa) detected | ||
Tai et al, 2013 [4] | Hippocampal homogenates (EFAD mice) | ELISA | SDS stable: E2FAD > E3FAD > E4FAD Total complex: E2FAD = E3FAD > E4FAD |
Human cortical synaptosomes (AD & NAD) | Total complex: | ||
• NAD > AD | |||
• NAD apoE33/Aβ = NAD apoE4X/Aβ > > AD apoE33/Aβ > AD apoE4X/Aβ | |||
SDS stable: | |||
• NAD apoE33/Aβ > > NAD apoE4X/Aβ & AD apoE33/Aβ > AD apoE4X/Aβ | |||
Human CSF (AD & NAD) | • NAD apoE33/Aβ > > NAD apoE4X/Aβ | ||
Verghese, et al, 2013 [65] | Human CSF (NAD) | SEC, ELISA | 95% Aβ (free) > > apoE33/Aβ = apoE44/Aβ |
No apoE isoform differences | |||
(In co-elution peak stoichiometric ratio of apoE:Aβ = 1:0.0002-0.0003) |