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Kamp, Frits; Scheidt, Holger A.; Winkler, Edith; Basset, Gabriele; Heinel, Hannes; Hutchison, James M.; LaPointe, Loren M.; Sanders, Charles R.; Steiner, Harald and Huster, Daniel (2018): Bexarotene Binds to the Amyloid Precursor Protein Transmembrane Domain, Alters Its alpha-Helical Conformation, and Inhibits gamma-Secretase Nonselectively in Liposomes. In: ACS Chemical Neuroscience, Vol. 9, No. 7: pp. 1702-1713

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Abstract

Bexarotene is a pleiotropic molecule that has been proposed as an amyloid-beta (A beta)-lowering drug for the treatment of Alzheimer's disease (AD). It acts by upregulation of an apolipoprotein E (apoE)-mediated A beta clearance mechanism. However, whether bexarotene induces removal of A beta plaques in mouse models of AD has been controversial. Here, we show by NMR and CD spectroscopy that bexarotene directly interacts with and stabilizes the transmembrane domain alpha-helix of the amyloid precursor protein (APP) in a region where cholesterol binds. This effect is not mediated by changes in membrane lipid packing, as bexarotene does not share with cholesterol the property of inducing phospholipid condensation. Bexarotene inhibited the intramembrane cleavage by gamma-secretase of the APP C-terminal fragment C99 to release A beta in cell-free assays of the reconstituted enzyme in liposomes, but not in cells, and only at very high micromolar concentrations. Surprisingly, in vitro, bexarotene also inhibited the cleavage of Notch1, another major gamma-secretase substrate, demonstrating that its inhibition of gamma-secretase is not substrate specific and not mediated by acting via the cholesterol binding site of C99. Our data suggest that bexarotene is a pleiotropic molecule that interfere with A beta metabolism through multiple mechanisms.

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