EDP Sciences logo
Submit your paper
Search
Menu
Home All issues Volume 25 / No 4 (July-August 2018) OCL, 25 4 (2018) D407 Full HTML
Open Access
Review
Issue
OCL
Volume 25, Number 4, July-August 2018
Article Number D407
Number of page(s) 6
Section Lipids & Brain IV: Lipids in Alzheimer’s Disease / Lipids & Brain IV : les lipides dans la maladie d’Alzheimer
DOI https://doi.org/10.1051/ocl/2018038
Published online 14 August 2018

© M.-C. Potier et al., Published by EDP Sciences, 2018

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

1 Introduction

Lipids are essential for brain function. Brain is one of the tissues with the highest lipid content, with up to 60% of dry matter. Amongst the various classes of lipids involved, such as fatty acids, phospholipids and cholesterol, membrane of neurons are particularly enriched in fatty acids and complex lipids.

Cholesterol is the major component of cellular membranes. Its insertion between phospholipids forming the membrane bilayer – composed of the internal leaflet facing the cytoplasm and the external leaflet isolating the cell from the extracellular environment – ensures the structure and stability of the membrane. Cholesterol fluidifies the membrane, thus avoiding crystallization of fatty acids. It also decreases membrane permeability to hydrosoluble molecules. In the membranes, cholesterol is enriched in lipid rafts, which are essential nanometric domains involved in anchoring functional molecules such as membrane receptors (Simons and Toomre, 2000; Simons and Gerl, 2010). In neurons, cholesterol is highly enriched in myelin sheaths and allows the propagation of nerve impulses by saltatory mechanisms.

Alzheimer’s disease (AD) is characterized by two abundant lesions, namely the extracellular amyloid plaques and the intracellular neurofibrillary tangles composed of hyperphosphorylated tau protein (Duyckaerts et al., 2009). Amyloid plaques are mainly composed of amyloidβ peptides (Aβ) produced by processing of the transmembrane Amyloid Precursor Protein APP by two sequential cleavages operated by the βsecretase BACE1 and the γsecretase acting in the membrane bilayer (Selkoe and Hardy, 2016). The amyloidogenic APP processing takes place in the endosomal compartment after internalization of APP where the environmental pH is suitable for enzyme activities (De Strooper and Annaert, 2010).

A large body of evidence from genetic, neuropathological and biochemical studies suggest strong links between cholesterol and AD, both in humans and in animal models of the disease (Cossec et al., 2010a).

2 Genetic risk factors for AD involved in cholesterol homeostasis

At least two genetic risk factors for AD are directly involved in cholesterol homeostasis (Lambert et al., 2013). The ε4 allele of the apolipoprotein gene APOE is 2.7 fold more frequent in AD patients (36.7%) as compared to the general population (13.7%) while the frequency of the ε3 allele is lower (59.4%) in AD patients as compared to the general population (77.9%) (Liu et al., 2013). Interestingly the ε2 allele is more frequent (8.4%) in the general population than in AD patients (3.9%). Isoform specific amino acid differences lie at codons 112 and 158 with ApoE4 bearing two Arg, ApoE2 two Cys and ApoE3 a Cys at codon 112 and an Arg at codon 158. APOE ε4 non-carriers have AD frequency of 20% with mean age of clinical onset at 84 while APOE ε4 heterozygous and homozygous are at 47% or 91%, with mean age of onset of 76 or 68, respectively (Liu et al., 2013). Thus the APOE ε4 has a very significant effect both on frequency and age of onset of AD. Recently we found that in a cohort of 318 participants aged 70–85 years with subjective memory complaints but unimpaired cognition and memory, 20% carried at least one ε4 allele. When stratified according to their brain amyloid load assessed by positron emission tomography (PET), 38% were ε4 among participants with Aβ deposition while the percentage dropped to 13% among participants with no Aβ deposition (Dubois et al., 2018). The APOE ε4 allele remains the highest genetic risk factor for AD. Besides, genetic meta-analysis identified another risk factor involved in cholesterol homeostasis: the ATP binding cassette ABC transporter 7 (ABCA7) gene. Intriguingly, ABCA7 has one of the strongest association with amyloid deposition, exceeded only by APOE ε4 (Apostolova et al., 2018).

3 Neuropathological studies showing increased cholesterol levels in the brain of AD patients

A number of converging studies point towards an increase in cholesterol levels in human autopsy brains of AD patients, compared to age-matched unaffected controls. Evidence from biochemical studies suggested membrane-associated oxidative stress, resulting in perturbed cholesterol metabolism and increased cholesterol levels in the middle frontal gyrus of AD patients (Cutler et al., 2004). Of note, the same authors also demonstrated that the increase in membrane-associated cholesterol correlated with the severity of cognitive deficits (Cutler et al., 2004). An independent biochemical and histochemical study also showed that cholesterol levels are increased in the occipital cortices of AD patients (Xiong et al., 2008). A liquid chromatography coupled with mass spectrometry approach identified twice as much cholesterol in laser microdissected-Aβ deposits from the isocortex of AD patients compared to the adjacent neuropil (Panchal et al., 2010). Using time-of-flight secondary ion mass spectrometry imaging on cortical human sections revealed that the cholesterol signal was significantly higher in the cortical layers III and IV of AD samples compared to controls (Lazar et al., 2012).

4 Biochemical evidence linking cholesterol, APP and its cleaving enzymes

Cholesterol in the adult brain is produced by astrocytes that can either recapture it from the extracellular compartment or synthesize it using their specific enzyme machinery (Shobab et al., 2005). Synthetized free cholesterol then binds to APOE and is transported across the cell membrane via the ABCA1 transporter. Lipoparticles will bind to low density lipoprotein receptor-related protein 1 (LRP1) present at the neuronal membrane and be internalized in the endolysosomal compartment where APOE is degraded and free cholesterol released and relocated into cholesterol enriched membrane domains. APP, BACE1 and the γsecretase protein complex are all localized in lipid rafts, suggesting a role of cholesterol in their processing activities (Bouillot et al., 1996; Cordy et al., 2003; Marquer et al., 2011). Indeed, an increase in cholesterol promoted γsecretase activity and amyloid peptides production (Matsumura et al., 2014). Other studies demonstrated that the palmitoylation of APP regulates its distribution in lipid rafts and its amyloidogenic processing (Bhattacharyya et al., 2013). The palmitoylation of BACE1 also regulates its enrichment in lipid rafts and although it does not affect its steady-state processing activity, it controls the synaptic activity-induced production of Aβ (Vetrivel et al., 2009; Andrew et al., 2017).

5 Structural evidence for a role of cholesterol on APP structure and dimerization at the membrane

Although APP is a transmembrane protein that is present in cholesterol enriched domains, its sequence does not contain any cholesterol recognition amino acid consensus sequence (CRAC) or inverted consensus sequence CARC (Fantini et al., 2016). However, a binding site for cholesterol on APP C-terminal fragment (βCTF) originating from the cleavage of APP by BACE1, has been predicted from structural studies using nuclear magnetic resonance (NMR) (Barrett et al., 2012). It was shown that the transmembrane and the juxtamembrane domains of βCTF are important for binding cholesterol, and molecular modelisation predicted that the transmembrane region of APP is a flexibly curved αhelix (Barrett et al., 2012). In addition, binding of cholesterol depends on the charge state of two amino acids (glutamic acid and aspartic acid at positions 22 and 23 of Aβ sequence, respectively) present in the juxtamembrane domain of APP. At low pH, these amino acids are neutral and bind cholesterol, while at higher pH, they are negatively charged and inserted deeper in the membrane (Panahi et al., 2016).

A competition between binding of APP to cholesterol and its dimerization has been suggested (Song et al., 2013), as similar portions of APP are involved in both functions. Indeed, initial studies with Aβ peptides showed that Aβ 29–42 is tilted and forms dimers in the membrane (Pillot et al., 1996). Moreover, dimerization of APP has been found to be due to the presence of GxxxG motifs in the transmembrane region (Kienlen-Campard et al., 2008). More precisely, the transmembrane motif G33XXXG37 and the juxtamembrane motif G25-SNK-G29 (numbering of Aβ sequence) facilitate the dimerization of APP and cholesterol helps to stabilize this interface (Tang et al., 2014). Another study showed that APP dimerization is 5 times higher than with the CTF fragment, highlighting the important role of the APP extramembrane domain (Kaden et al., 2008; Ben Khalifa et al., 2012; Decock et al., 2015; Nierzwicki and Czub, 2015). Modelisation studies showed that the transmembrane helix of APP self-associates in left-handed parallel dimer while the juxtamembrane helix senses dimerization (Nadezhdin et al., 2012). Of note, the dimerization motif GxxxG is not sufficient for cholesterol binding and the juxtamembrane domain is required (Nierzwicki and Czub, 2015). Finally, a recent study showed that the transmembrane motif V39XXA42T43XXV46XXXV50 is involved in the dimerization of C99 and binds lipid rafts (Sun et al., 2017).

6 The role of cholesterol on APP endocytosis and processing

Since APP is a transmembrane protein that can interact with cholesterol, and cholesterol levels are increased in AD, we studied the role of cholesterol on APP processing and amyloid pathology. We used methyβcyclodextrin (MBCD) to decrease cholesterol and MBCD-cholesterol complex to deliver cholesterol locally at the plasma membrane of living cells. Indeed, molecular dynamic studies have shown that MBCD can extract cholesterol from the plasma membrane (Lopez et al., 2011). We chose not to modulate the activity of cholesterol synthesis enzymes, such as 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase (HMGCR), because of strong compensatory effects that take place when knocking down HMGCR (data unpublished).

We demonstrated that, in HEK293 cells, membrane cholesterol levels control APP endocytosis and this effect is dependent on clathrin, the small GTPase Rab5 and dynamin2 (Cossec et al., 2010b). Dynamin2 is associated with clathrin-coated pit maturation and fission of the membrane neck of coated pits. Rab5 regulates membrane fusion between early endosomes and their maturation through interaction with phosphatidylinositol 3-phosphate (PtdIns3P) and the early endosomal antigen 1 (EEA1). We found that the effect of cholesterol on APP endocytosis was inhibited by either transfecting dominant negative mutants of Rab5 or dynamin2 that cannot be activated, or by treating cells with siRNA against clathrin (Cossec et al., 2010b).

Using fluorescence activated cell sorting (FACS), we confirmed that APP endocytosis is promoted by cholesterol increase in a dose-dependent manner (Cossec et al., 2010b). To explore the specificity of the effect of cholesterol levels on internalization, we tested it on the cannabinoid 1 (CB1) and the transferrin receptors, and found that an increase of cholesterol at the plasma membrane only slightly promoted their internalization. In contrast, APP endocytosis was much more sensitive to the levels of cholesterol. In addition, we found that cholesterol treatment increased APP internalization in endosomes that appeared larger than in untreated cells. There was a significant increase of Aβ40 and Aβ42 secretion in HEK293 cells transfected with APP bearing the Swedish mutations and treated with MBCD-cholesterol complex. This effect was dependent on the extent of the cholesterol increase at the plasma membrane and on APP internalization, as demonstrated by clathrin knock-down experiments (Cossec et al., 2010b). A similar effect of cholesterol on endogenous Aβ42 secretion was reproduced in primary rat hippocampal neurons, although, in this case, Aβ40 was unchanged and Aβ38 was decreased (Marquer et al., 2014).

Increase of Aβ secretion following cholesterol treatment could be due to either an effect on BACE1 activity or to a facilitation of APP-BACE1 proximity. After showing that induced cholesterol increase at the plasma membrane had no effect on BACE1 catalytic activity, we thought to study the interaction of APP and BACE1 at the plasma membrane of primary neurons in culture (Marquer et al., 2011). Rat hippocampal neurons were transfected with APP-mCherry and BACE1-GFP constructs and imaged using Fluorescence Lifetime Imaging Microscopy (FLIM). When the distance between the two proteins (BACE1-GFP donor and APP-mCherry acceptor) is below 10 nm, Förster Resonance Energy Transfer (FRET) can occur and the fluorescence lifetime of the donor decreases. By Total Internal Reflection Fluorescence (TIRF) imaging, we could demonstrate that increase of cholesterol favors APP-BACE1 proximity at the plasma membrane. We then wondered whether this happened in specific regions of the plasma membrane enriched in cholesterol (lipid rafts). We used Fluorescence Correlation Spectroscopy (FCS) to measure the diffusion coefficients of APP-YFP molecules (Marquer et al., 2012). We showed that about 7 min after cholesterol treatment, APP-YFP relocalized to lipid rafts where diffusion time is higher as compared to non-raft portions of the plasma membrane (Marquer et al., 2011). This peak was followed by an extinction of fluorescence signal attributed to the internalization of APP-YFP, since this fluorescence decrease was inhibited by dynasore treatment and corresponded to the time of internalization through the clathrin-dependant pathway. Taken together, our microscopy studies strongly suggest that, in normal conditions, APP and BACE1 are distributed inside and outside of lipid rafts. However, less than 10 min after treatment with MBCD-cholesterol, APP and BACE1 are relocalized in lipid rafts that have either higher levels of cholesterol or expand their size with similar levels of cholesterol per surface unit. This event is rapidly followed by internalization in early endosomes that have greater size (Fig. 1).

Altogether, we show that modulating cholesterol levels to the extent of what is observed in human AD autopsy brains (+ 30%) results in increased APP and BACE1 proximity and in their endocytosis in enlarged early endosomes, leading to the overproduction of Aβ peptides. This enlarged endosome phenotype is reminiscent of what has been described in pyramidal cells from postmortem human brain.

thumbnail Fig. 1 Effects of artificial increase of cholesterol at the cellular plasma membrane.

In the control condition, APP and BACE1 are present inside and outside lipid rafts at the plasma membrane. Raising cholesterol at the plasma membrane induces: i) relocalization of APP and BACE1 in lipid rafts and their rapid internalization assessed by Fluorescence correlation Spectroscopy in enlarged and clustered endosomes (Marquer et al., 2011; Marquer et al., 2014); ii) increase of APP and BACE1 proximity assessed by Total Internal Reflection Fluorescence-Fluorescence Lifetime Imaging-Förster Resonance Energy Transfer (TIRF-FLIM-FRET) microscopy (Marquer et al., 2011); iii) increase of production of Aβ peptides (Cossec et al., 2010a; Cossec et al., 2010b; Marquer et al., 2014).

7 Increasing neuronal cholesterol levels recapitulates AD phenotypes

We also explored whether, in addition to its effect on Aβ levels, increasing cholesterol could also lead to other cellular phenotypes reminiscent of AD. As previously mentioned, one of the earliest phenotypes of human AD is the enlargement of early endosomes (Cataldo et al., 2000). We found that treatment of primary rat hippocampal neurons with MBCD-cholesterol to reach a 30% increase, induced a change in the endosomal compartment with an increase in the mean volume of early endosomes, as assessed by confocal microscopy (Marquer et al., 2014). Using transmission electron microscopy, we found that not only the surface of early endosomes was increased but they also formed clusters. Another key feature of AD dysfunction is axonal transport deficits (Dai et al., 2002). We thus analyzed axonal transport of APP. Hippocampal neurons were transfected with APP-mCherry and treated with MBCD-cholesterol for 20–35 min and APP-mCherry containing vesicles were followed using live imaging. We found a very significant decrease of APP anterograde transport after cholesterol increase, while retrograde transport remained unchanged (Marquer et al., 2014). Finally and in order to find out whether cholesterol treated neurons had a similar transcripts signature as compared to neurons from postmortem human brain samples, we compared the transcriptome of treated neurons to the ones from brain samples at different Braak stages of AD. Hierarchical clustering analysis highlighted that gene expression profile of cholesterol-treated neurons were similar to early AD stages, suggesting that cholesterol increase could be an early phenotype during the course of the disease, either occurring as a primary or secondary event (Marquer et al., 2014). Among the genes differentially expressed following cholesterol increase, Gene Ontology category enrichment analysis revealed that cholesterol pathway, response to lipid, sterol biosynthetic pathways were the most enriched categories.

Thus, increase in neuronal membrane cholesterol promotes APP processing and endocytosis, enlargement of early endosomes and axonal transport abnormalities, inducing gene expression modifications similar to the ones detected in early stages of AD. Changes in membrane cholesterol linked with age could thus be a starting event triggering sporadic AD.

This postulate based on evidence collected in neuronal cultures is supported by in vivo studies. For example, inhibiting CYP46A1, the enzyme that hydroxylates cholesterol at position 24, allowing its passage through the blood brain barrier and the decrease of cholesterol levels in the brain, worsens AD phenotypes. Specifically, CYP46A1 inhibition leads to brain cholesterol accumulation, endoplasmic reticulum stress, increase of βCTF and Aβ production, tau hyperphosphorylation and hippocampal atrophy linked to neuronal death, supporting that high neuronal cholesterol could induce or accelerate the course of sporadic AD (Djelti et al., 2015). In addition, crossing APP/PS1 mice with mice overexpressing sterol regulatory element-binding protein-2 (SREBP2) induced mitochondrial cholesterol accumulation, oxidative damage and Aβ accumulation as well as, very interestingly, tau phosphorylation and neurofibrillary tangle formation that had never been detected before in any mouse model reproducing the amyloid pathology (Barbero-Camps et al., 2013).

8 Towards decreasing neuronal membrane cholesterol to delay/counteract sporadic AD

Specifically decreasing neuronal cholesterol thus appears like a promising strategy to either delay or counteract the development of sporadic AD. Several studies in mouse models convincingly support this hypothesis. Injection of adenoviral constructs expressing CYP46A1 in mouse models of AD reproducing either the amyloid or the tau pathologies improves cognitive function and reduces amyloid pathology as well as tau hyperphosphorylation (Hudry et al., 2010; Burlot et al., 2015). CYP46A1 knock-out mice have severe memory deficits (Kotti et al., 2006) while older transgenic mice overexpressing CYP46A1 show improved cognitive performance (Maioli et al., 2013). In addition, treatment of AD mice overexpressing APP with the Swedish mutations with hydroxypropyl-β-cyclodextrin reduced the number of amyloid plaques, increased the expression of genes involved in cholesterol transport and Aβ clearance, and improved spatial learning and memory deficits (Yao and Papadopoulos, 2002), thus showing clear neuroprotective effects.

Finally replacing membrane cholesterol with stigmasterol, a plant sterol crossing the blood brain barrier, decreased APP processing and the production of Aβ peptides. Mice under stigmasterol-rich diet had decreased amyloidogenic APP processing (Burg et al., 2013). On the contrary, high cholesterol diet in a transgenic mouse model expressing Swedish and London mutations disturbs the integrity of the BBB, increases Aβ in the brains and decreases Aβ in the plasma of these mice (Loffler et al., 2016).

In total, results from these studies, using various strategies to decrease neuronal cholesterol, converge towards the conclusion that lowering cholesterol levels in the brain is indeed beneficial and alleviates an array of AD phenotypes.

9 Conclusions

Since the identification of the cholesterol transporter APOE ε4 haplotype as the highest genetic risk factor for AD (Mayeux et al., 1993), much has been done to understand the role of cholesterol metabolism in the pathogenesis of AD (Allinquant et al., 2014). We deliberately omitted all the work performed with statins, since most of the clinical and molecular studies have not been conclusive so far (Yasar and Whitmer, 2018). A significant body of work points to a deleterious role of neuronal cholesterol in the development of sporadic AD. Amongst these, molecular studies and new microscopies allowing the analysis of sub compartments of the plasma membrane provided definitive evidence of this role. Measuring in situ cholesterol levels in postmortem human brain samples remains a challenge. Without any selective antibodies, we are left with very few markers that remain extremely difficult to utilize. Some therapies have been tested preclinically in mouse models of AD but much remains to be done in clinical research to validate possible targets and food supplements in order to delay or counteract sporadic AD. Finally, a more precise molecular analysis of the APP cholesterol binding site and the important yet misunderstood interplay with APOE genotype might bring new insights into the field and pave the way to unprecedented therapeutic avenues.

Disclosure

The authors disclose any conflict of interest.

Acknowledgements

The authors wish to thank Institut de Recherche Servier and the program “Investissements d’avenir” ANR-10-IAIHU-06 for their financial support. LH had a fellowship from Institut de Recherche Servier.

References

  • Allinquant B, Clamagirand C, Potier MC. 2014. Role of cholesterol metabolism in the pathogenesis of Alzheimer’s disease. Curr Opin Clin Nutr Metab Care 17: 319–323. [CrossRef] [PubMed] [Google Scholar]
  • Andrew RJ, Fernandez CG, Stanley M, et al. 2017. Lack of BACE1 S-palmitoylation reduces amyloid burden and mitigates memory deficits in transgenic mouse models of Alzheimer’s disease. Proc Natl Acad Sci USA 114: E9665–E9674. [CrossRef] [Google Scholar]
  • Apostolova LG, Risacher SL, Duran T, et al. 2018. Associations of the top 20 Alzheimer disease risk variants with brain amyloidosis. JAMA Neurol 75: 328–341. [CrossRef] [PubMed] [Google Scholar]
  • Barbero-Camps E, Fernandez A, Martinez L, Fernandez-Checa JC, Colell A. 2013. APP/PS1 mice overexpressing SREBP-2 exhibit combined Abeta accumulation and tau pathology underlying Alzheimer’s disease. Hum Mol Genet 22: 3460–3476. [CrossRef] [PubMed] [Google Scholar]
  • Barrett PJ, Song Y, Van Horn WD, et al. 2012. The amyloid precursor protein has a flexible transmembrane domain and binds cholesterol. Science 336: 1168–1171. [CrossRef] [Google Scholar]
  • Ben Khalifa N, Tyteca D, Marinangeli C, et al. 2012. Structural features of the KPI domain control APP dimerization, trafficking, and processing. FASEB J 26: 855–867. [Google Scholar]
  • Bhattacharyya R, Barren C, Kovacs DM. 2013. Palmitoylation of amyloid precursor protein regulates amyloidogenic processing in lipid rafts. J Neurosci 33: 11169–11183. [CrossRef] [PubMed] [Google Scholar]
  • Bouillot C, Prochiantz A, Rougon G, Allinquant B. 1996. Axonal amyloid precursor protein expressed by neurons in vitro is present in a membrane fraction with caveolae-like properties. J Biol Chem 271: 7640–7644. [CrossRef] [PubMed] [Google Scholar]
  • Burg VK, Grimm HS, Rothhaar TL, et al. 2013. Plant sterols the better cholesterol in Alzheimer’s disease? A mechanistical study. J Neurosci 33: 16072–16087. [CrossRef] [PubMed] [Google Scholar]
  • Burlot MA, Braudeau J, Michaelsen-Preusse K, et al. 2015. Cholesterol 24-hydroxylase defect is implicated in memory impairments associated with Alzheimer-like Tau pathology. Hum Mol Genet 24: 5965–5976. [CrossRef] [PubMed] [Google Scholar]
  • Cataldo AM, Peterhoff CM, Troncoso JC, Gomez-Isla T, Hyman BT, Nixon RA. 2000. Endocytic pathway abnormalities precede amyloid beta deposition in sporadic Alzheimer’s disease and Down syndrome: differential effects of APOE genotype and presenilin mutations. Am J Pathol 157: 277–286. [CrossRef] [PubMed] [Google Scholar]
  • Cordy JM, Hussain I, Dingwall C, Hooper NM, Turner AJ. 2003. Exclusively targeting beta-secretase to lipid rafts by GPI-anchor addition up-regulates beta-site processing of the amyloid precursor protein. Proc Natl Acad Sci USA 100: 11735–11740. [CrossRef] [Google Scholar]
  • Cossec JC, Marquer C, Panchal M, Lazar AN, Duyckaerts C, Potier MC. 2010a. Cholesterol changes in Alzheimer’s disease: Methods of analysis and impact on the formation of enlarged endosomes. Biochim Biophys Acta 1801: 839–845. [Google Scholar]
  • Cossec JC, Simon A, Marquer C, et al. 2010b. Clathrin-dependent APP endocytosis and Abeta secretion are highly sensitive to the level of plasma membrane cholesterol. Biochim Biophys Acta 1801: 846–852. [CrossRef] [PubMed] [Google Scholar]
  • Cutler RG, Kelly J, Storie K, et al. 2004. Involvement of oxidative stress-induced abnormalities in ceramide and cholesterol metabolism in brain aging and Alzheimer’s disease. Proc Natl Acad Sci USA 101: 2070–2075. [CrossRef] [Google Scholar]
  • Dai J, Buijs RM, Kamphorst W, Swaab DF. 2002. Impaired axonal transport of cortical neurons in Alzheimer’s disease is associated with neuropathological changes. Brain Res 948: 138–144. [Google Scholar]
  • De Strooper B, Annaert W. 2010. Novel research horizons for presenilins and gamma-secretases in cell biology and disease. Annu Rev Cell Dev Biol 26: 235–260. [CrossRef] [Google Scholar]
  • Decock M, El Haylani L, Stanga S, et al. 2015. Analysis by a highly sensitive split luciferase assay of the regions involved in APP dimerization and its impact on processing. FEBS Open Bio 5: 763–773. [Google Scholar]
  • Djelti F, Braudeau J, Hudry E, et al. 2015. CYP46A1 inhibition, brain cholesterol accumulation and neurodegeneration pave the way for Alzheimer’s disease. Brain 138: 2383–2398. [CrossRef] [PubMed] [Google Scholar]
  • Dubois B, Epelbaum S, Nyasse F, et al. 2018. Cognitive and neuroimaging features and brain beta-amyloidosis in individuals at risk of Alzheimer’s disease (INSIGHT-preAD): a longitudinal observational study. Lancet neurology 17: 335–346. [CrossRef] [Google Scholar]
  • Duyckaerts C, Delatour B, Potier MC. 2009. Classification and basic pathology of Alzheimer disease. Acta Neuropathol 118: 5–36. [CrossRef] [PubMed] [Google Scholar]
  • Fantini J, Di Scala C, Evans LS, Williamson PT, Barrantes FJ. 2016. A mirror code for protein-cholesterol interactions in the two leaflets of biological membranes. Sci Rep 6: 21907. [CrossRef] [PubMed] [Google Scholar]
  • Hudry E, Van Dam D, Kulik W, et al. 2010. Adeno-associated virus gene therapy with cholesterol 24-hydroxylase reduces the amyloid pathology before or after the onset of amyloid plaques in mouse models of Alzheimer’s disease. Mol Ther 18: 44–53. [CrossRef] [PubMed] [Google Scholar]
  • Kaden D, Munter LM, Joshi M, et al. 2008. Homophilic interactions of the amyloid precursor protein (APP) ectodomain are regulated by the loop region and affect {beta}-secretase cleavage of APP. J Biol Chem 283: 7271–7279. [CrossRef] [PubMed] [Google Scholar]
  • Kienlen-Campard P, Tasiaux B, Van Hees J, et al. 2008. Amyloidogenic processing but not amyloid precursor protein (APP) intracellular C-terminal domain production requires a precisely oriented APP dimer assembled by transmembrane GXXXG motifs. J Biol Chem 283: 7733–7744. [CrossRef] [PubMed] [Google Scholar]
  • Kotti TJ, Ramirez DM, Pfeiffer BE, Huber KM, Russell DW. 2006. Brain cholesterol turnover required for geranylgeraniol production and learning in mice. Proc Natl Acad Sci USA 103: 3869–3874. [CrossRef] [Google Scholar]
  • Lambert JC, Ibrahim-Verbaas CA, Harold D, et al. 2013. Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer’s disease. Nat Genet 45: 1452–1458. [CrossRef] [PubMed] [Google Scholar]
  • Lazar AN, Bich C, Panchal M, et al. 2012. Time-of-flight secondary ion mass spectrometry (TOF-SIMS) imaging reveals cholesterol overload in the cerebral cortex of Alzheimer disease patients. Acta Neuropathol 125: 133–144. [CrossRef] [PubMed] [Google Scholar]
  • Liu CC, Kanekiyo T, Xu H, Bu G. 2013. Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy. Nat Rev Neurol 9: 106–118. [CrossRef] [PubMed] [Google Scholar]
  • Loffler T, Flunkert S, Temmel M, Hutter-Paier B. 2016. Decreased plasma abeta in hyperlipidemic APPSL transgenic mice is associated with BBB dysfunction. Front Neurosci 10: 232. [CrossRef] [Google Scholar]
  • Lopez CA, de Vries AH, Marrink SJ. 2011. Molecular mechanism of cyclodextrin mediated cholesterol extraction. PLoS comput biol 7: e1002020. [Google Scholar]
  • Maioli S, Bavner A, Ali Z, et al. 2013. Is it possible to improve memory function by upregulation of the cholesterol 24S-hydroxylase (CYP46A1) in the brain? PLoS One 8: e68534. [Google Scholar]
  • Marquer C, Devauges V, Cossec JC, et al. 2011. Local cholesterol increase triggers amyloid precursor protein-Bace1 clustering in lipid rafts and rapid endocytosis. FASEB J 25: 1295–1305. [CrossRef] [PubMed] [Google Scholar]
  • Marquer C, Laine J, Dauphinot L, et al. 2014. Increasing membrane cholesterol of neurons in culture recapitulates Alzheimer’s disease early phenotypes. Mol neurodegener 9: 60. [CrossRef] [PubMed] [Google Scholar]
  • Marquer C, Leveque-Fort S, Potier MC. 2012. Determination of lipid raft partitioning of fluorescently-tagged probes in living cells by fluorescence correlation spectroscopy (FCS). J Vis Exp 62: e3513. [Google Scholar]
  • Matsumura N, Takami M, Okochi M, et al. 2014. Gamma-Secretase associated with lipid rafts: multiple interactive pathways in the stepwise processing of beta-carboxyl-terminal fragment. J Biol Chem 289: 5109–5121. [CrossRef] [PubMed] [Google Scholar]
  • Mayeux R, Stern Y, Ottman R, et al. 1993. The apolipoprotein epsilon 4 allele in patients with Alzheimer’s disease. Ann Neurol 34: 752–754. [CrossRef] [PubMed] [Google Scholar]
  • Nadezhdin KD, Bocharova OV, Bocharov EV, Arseniev AS. 2012. Dimeric structure of transmembrane domain of amyloid precursor protein in micellar environment. FEBS Lett 586: 1687–1692. [CrossRef] [PubMed] [Google Scholar]
  • Nierzwicki L, Czub J. 2015. Specific binding of cholesterol to the amyloid precursor protein: structure of the complex and driving forces characterized in molecular detail. J Phys Chem Lett 6: 784–790. [CrossRef] [PubMed] [Google Scholar]
  • Panahi A, Bandara A, Pantelopulos GA, Dominguez L, Straub, JE. 2016. Specific binding of cholesterol to C99 domain of amyloid precursor protein depends critically on charge state of protein. J Phys Chem Lett 7: 3535–3541. [CrossRef] [PubMed] [Google Scholar]
  • Panchal M, Loeper J, Cossec JC, et al. 2010. Enrichment of cholesterol in microdissected Alzheimer’s disease senile plaques as assessed by mass spectrometry. J Lipid Res 51: 598–605. [CrossRef] [PubMed] [Google Scholar]
  • Pillot T, Goethals M, Vanloo B, et al. 1996. Fusogenic properties of the C-terminal domain of the Alzheimer beta-amyloid peptide. J Biol Chem 271: 28757–28765. [CrossRef] [PubMed] [Google Scholar]
  • Selkoe DJ, Hardy J. 2016. The amyloid hypothesis of Alzheimer’s disease at 25 years. EMBO mol med 8: 595–608. [Google Scholar]
  • Shobab LA, Hsiung GY, Feldman HH. 2005. Cholesterol in Alzheimer’s disease. Lancet neurology 4: 841–852. [CrossRef] [PubMed] [Google Scholar]
  • Simons K, Gerl MJ. 2010. Revitalizing membrane rafts: new tools and insights. Nat Rev Mol Cell Biol 11: 688–699. [Google Scholar]
  • Simons K, Toomre D. 2000. Lipid rafts and signal transduction. Nat Rev Mol Cell Biol 1: 31–39. [CrossRef] [PubMed] [Google Scholar]
  • Song Y, Hustedt EJ, Brandon S, Sanders CR. 2013. Competition between homodimerization and cholesterol binding to the C99 domain of the amyloid precursor protein. Biochemistry 52: 5051–5064. [CrossRef] [PubMed] [Google Scholar]
  • Sun F, Chen L, Wei P, et al. 2017. Dimerization and structural stability of amyloid precursor proteins affected by the membrane microenvironments. J Chem Inf Model 57: 1375–1387. [CrossRef] [PubMed] [Google Scholar]
  • Tang TC, Hu Y, Kienlen-Campard P, et al. 2014. Conformational changes induced by the A21G Flemish mutation in the amyloid precursor protein lead to increased Abeta production. Structure 22: 387–396. [CrossRef] [PubMed] [Google Scholar]
  • Vetrivel KS, Meckler X, Chen Y, et al. 2009. Alzheimer disease Abeta production in the absence of S-palmitoylation-dependent targeting of BACE1 to lipid rafts. J Biol Chem 284: 3793–3803. [CrossRef] [PubMed] [Google Scholar]
  • Xiong H, Callaghan D, Jones A, et al. 2008. Cholesterol retention in Alzheimer’s brain is responsible for high beta- and gamma-secretase activities and A beta production. Neurobiol Dis 29: 422–437. [CrossRef] [PubMed] [Google Scholar]
  • Yao ZX, Papadopoulos V. 2002. Function of beta-amyloid in cholesterol transport: a lead to neurotoxicity. Faseb J 16: 1677–1679. [CrossRef] [PubMed] [Google Scholar]
  • Yasar S, Whitmer R. 2018. Statin use and risk of Alzheimer disease: A new view on an old relationship. Neurology 90: 103–104. [CrossRef] [PubMed] [Google Scholar]

Cite this article as: Potier M-C, Hanbouch L, Marquer C. 2018. Cholesterol and ApoE in Alzheimer’s disease. OCL 25(4): D407.

All Figures

thumbnail Fig. 1 Effects of artificial increase of cholesterol at the cellular plasma membrane.

In the control condition, APP and BACE1 are present inside and outside lipid rafts at the plasma membrane. Raising cholesterol at the plasma membrane induces: i) relocalization of APP and BACE1 in lipid rafts and their rapid internalization assessed by Fluorescence correlation Spectroscopy in enlarged and clustered endosomes (Marquer et al., 2011; Marquer et al., 2014); ii) increase of APP and BACE1 proximity assessed by Total Internal Reflection Fluorescence-Fluorescence Lifetime Imaging-Förster Resonance Energy Transfer (TIRF-FLIM-FRET) microscopy (Marquer et al., 2011); iii) increase of production of Aβ peptides (Cossec et al., 2010a; Cossec et al., 2010b; Marquer et al., 2014).
In the text

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.