Lipid-protecting disulfide bridges are the missing molecular link between ApoE4 and sporadic Alzheimers disease in humans
Ramsden, C. E.; Cutler, R. G.; Li, X.; Keyes, G. S.
Show abstract
As the principal lipid transporter in the human brain, apolipoprotein E (ApoE) is tasked with the transport and protection of highly vulnerable lipids required to support and remodel neuronal membranes, in a process that is dependent on ApoE receptors. Human APOE allele variants that encode proteins differing only in the number of cysteine (Cys)-to-arginine (Arg) exchanges (ApoE2 [2 Cys], ApoE3 [1 Cys], ApoE4 [0 Cys]) comprise the strongest genetic risk factor for sporadic Alzheimers disease (AD); however, the specific molecular feature(s) and resultant mechanisms that underlie these isoform-dependent effects are unknown. One signature feature of Cys is the capacity to form disulfide (Cys-Cys) bridges, which are required to form disulfide bridge-linked dimers and multimers. Here we propose the overarching hypothesis that the super-ability (for ApoE2), intermediate ability (for ApoE3) or inability (for ApoE4) to form lipid-protecting intermolecular disulfide bridges, is the central molecular determinant accounting for the disparate effects of APOE alleles on AD risk and amyloid-{beta} and Tau pathologies in humans. We posit that presence and abundance of Cys in human ApoE3 and ApoE2 respectively, conceal and protect vulnerable lipids transported by ApoE from peroxidation by enabling formation of ApoE homo-dimers/multimers and heteromeric ApoE complexes such as ApoE-ApoJ and ApoE-ApoD. We thus propose that the inability to form intermolecular disulfide bridges makes ApoE4-containing lipoproteins uniquely vulnerable to peroxidation and its downstream consequences. Consistent with our model, we found that brain-enriched polyunsaturated fatty acid-containing phospholipids induce disulfide-dependent dimerization and multimerization of ApoE3 and ApoE2 (but not ApoE4). By contrast, incubation with the peroxidation-resistant lipid DMPC or cholesterol alone had minimal effects on dimerization. These novel concepts and findings are integrated into our unifying model implicating peroxidation of ApoE-containing lipoproteins, with consequent ApoE receptor-ligand disruption, as the initiating molecular events that ultimately lead to AD in humans. HighlightsO_LIAPOE alleles are the strongest genetic risk factor for sporadic Alzheimers disease (AD) C_LIO_LIAPOE alleles encode proteins that differ only in the number of Cys{longrightarrow}Arg exchanges C_LIO_LIDespite 30 years of inquiry, mechanisms linking Cys{longrightarrow}Arg exchanges to AD remain unknown C_LIO_LIPUFA-phospholipids induced disulfide bridge formation in ApoE3 and ApoE2 (but not ApoE4) C_LIO_LIWe hypothesize that disulfide bridges in ApoE protect vulnerable lipids from peroxidation C_LIO_LIWe propose that lipid-protecting disulfide bridges explain APOE allele-dependent AD risks C_LI
Matching journals
The top 7 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- LACK OF OXYGEN AND/OR GLUCOSE DIFFERENTIALLY POTENTIATES Aβ40E22Q- AND Aβ42-INDUCED CEREBRAL ENDOTHELIAL CELL DEATH, BARRIER DYSFUNCTION AND ANGIOGENESIS IMPAIRMENT 92%
- The role of Aβ circRNA in Alzheimer's disease: alternative mechanism of Aβ biogenesis from Aβ circRNA translation 91%
- Age-related increases in PDE11A4 protein expression trigger liquid:liquid phase separation (LLPS) of the enzyme that can be reversed by PDE11A4 small molecules inhibitors 91%
Similar papers in this journal
- Serum metabolome profiling in patients with mild cognitive impairment reveals sex differences in lipid metabolism 93%
- Retinal tau phosphorylation in Alzheimer's disease: a mass spectrometry study 92%
- Leptin reduces pathology and increases adult neurogenesis in a transgenic mouse model of Alzheimer’s disease 92%
Similar papers in this journal
- APOE Genotype Influences on The Brain Metabolome of Aging Mice - Role for Mitochondrial Energetics in Mechanisms of Resilience in APOE2 Genotype. 94%
- Diabetic phenotype in mouse and humans with β-amyloid pathology reduces the number of microglia around β-amyloid plaques 94%
- Genetic perturbations of disease risk genes in mice capture transcriptomic signatures of late-onset Alzheimer’s disease 93%
Similar papers in this journal
- Lipid peroxidation induced ApoE receptor-ligand disruption as a unifying hypothesis underlying sporadic Alzheimer’s disease in humans 94%
- Trimethylamine N-oxide reduces neurite density and plaque intensity in a murine model of Alzheimer disease 94%
- Relationships of Alzheimer’s disease and apolipoprotein E genotypes with small RNA and protein cargo of brain tissue extracellular vesicles 93%