Abstract
The ε4 allele of apolipoprotein E gene is a major risk factor for Alzheimer's disease. However, the mechanism by which the E4 isoform of apolipoprotein E increases the risk of Alzheimer's disease is poorly understood. To determine whether the isoform-specific effects of apolipoprotein E may be mediated via clearance of bound β-amyloid, we examined the uptake of β-amyloid 1-40 into Chinese hamster ovary cells in the presence or absence of the apolipoprotein E isoforms E2, E3 and E4. Apolipoprotein E2 and E3 treatments were associated with higher association of β-amyloid with cells as compared to treatment with E4. Heparin blocked the association of β-amyloid with cells, as did an antibody to one of the apolipoprotein E receptors (the low-density lipoprotein receptor-related protein). Thus, the apolipoproteins E2 and E3, but not E4, may play important roles in the clearance of β-amyloid from the extracellular space via the low-density lipoprotein receptor-related protein.
| Original language | English |
|---|---|
| Pages (from-to) | 1217-1226 |
| Number of pages | 10 |
| Journal | Neuroscience |
| Volume | 90 |
| Issue number | 4 |
| DOIs | |
| State | Published - Jun 1999 |
| Externally published | Yes |
Keywords
- Alzheimer's disease
- Apolipoprotein E
- Chinese hamster ovary cells
- Heparan sulphate proteoglycans
- LDL receptor- related protein
- β-amyloid
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