Cell Stem Cell
Volume 24, Issue 3, 7 March 2019, Pages 363-375.e9
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Article
Cholesterol Metabolism Is a Druggable Axis that Independently Regulates Tau and Amyloid-β in iPSC-Derived Alzheimer’s Disease Neurons

https://doi.org/10.1016/j.stem.2018.12.013Get rights and content
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Highlights

  • Drug screening identifies inhibitors of aberrant phosphorylated Tau (pTau) accumulation

  • Cholesteryl esters (CE) were identified as upstream regulators of pTau proteostasis

  • The effects of CE on Tau proteostasis are correlated with, but independent of, APP and Aβ

  • Lead compound enhance CE-dependent pTau proteasomal turnover specifically in neurons

Summary

Genetic, epidemiologic, and biochemical evidence suggests that predisposition to Alzheimer’s disease (AD) may arise from altered cholesterol metabolism, although the molecular pathways that may link cholesterol to AD phenotypes are only partially understood. Here, we perform a phenotypic screen for pTau accumulation in AD-patient iPSC-derived neurons and identify cholesteryl esters (CE), the storage product of excess cholesterol, as upstream regulators of Tau early during AD development. Using isogenic induced pluripotent stem cell (iPSC) lines carrying mutations in the cholesterol-binding domain of APP or APP null alleles, we found that while CE also regulate Aβ secretion, the effects of CE on Tau and Aβ are mediated by independent pathways. Efficacy and toxicity screening in iPSC-derived astrocytes and neurons showed that allosteric activation of CYP46A1 lowers CE specifically in neurons and is well tolerated by astrocytes. These data reveal that CE independently regulate Tau and Aβ and identify a druggable CYP46A1-CE-Tau axis in AD.

Keywords

Alzheimer’s disease
induced pluripotent stem cells
disease modeling
drug screening
lipids
cholesterol metabolism
cholesteryl esters
CYP46A1 Tau
amyloid beta
proteostasis

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