Sci. STKE, 16 October 2007
Apolipoprotein E Cholesterol and Alzheimers Disease
John F. Foley
Sciences STKE, AAAS, Washington, DC 20005, USA
The relationship between the abundance of cholesterol in the brain and Alzheimers disease (AD) progression is a controversial one, although cholesterol is necessary for neuronal function. Because the 4 allele of the gene encoding apolipoprotein E (apoE), a lipoprotein that transports cholesterol, is a genetic risk factor for late-onset AD, Liu et al. investigated a link between amyloid precursor protein (APP), apoE, and cholesterol metabolism. Sequential cleavage of APP, a transmembrane protein, by -secretase and -secretase releases amyloid -peptide (A) and the APP intracellular domain (AICD) into the extracellular space, where the former forms plaques. The authors found that the abundance of apoE (as measured by enzyme-linked immunosorbent assay) was lower in the brains of APP-deficient mice (APP-KO) and mice deficient in both APP and the related APLP2 (DKO) than in wild-type mice. Real-time polymerase chain reaction and Western blotting analyses showed that the abundance of the apoE receptor LRP1 was higher in APP-KO and DKO mice than in wild-type controls. Brain-specific deletion of LRP1 resulted in the higher abundance of apoE in the brains of these mice than in the brains of wild-type mice. Deletion of the gene encoding -secretase, which is required for A production, had no effect on LRP1 abundance or function. However, deletion of both presenilin 1 (PS1) and PS2 (PS DKO), which encode proteins critical to the function of -secretase, resulted in the higher abundance of LRP1 in PS DKO mice compared with that of wild-type mice. Further analysis showed that the AICD, released through -secretase activity, combined with the adaptor protein Fe65 and bound to the LRP1 promoter, inhibiting its expression. Thus, APP processing by -secretase results in the decreased abundance of LRP1, which results in the reduced uptake of apoE-complexed cholesterol. Together, these data suggest a role for APP in regulating apoE and cholesterol metabolism, through the lipoprotein receptor LRP1, which provides new therapeutic targets for treating AD.
Q. Liu, C. V. Zerbinatti, J. Zhang, H.-S. Hoe, B. Wang, S. L. Cole, J. Herz, L. Muglia, G. Bu, Amyloid precursor protein regulates brain apolipoprotein E and cholesterol metabolism through lipoprotein receptor LRP1. Neuron 56, 66-78 (2007). [PubMed]
Citation: J. F. Foley, Cholesterol and Alzheimers Disease. Sci. STKE 2007, tw375 (2007).
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