- Research article
- Open Access
Apolipoprotein-E forms dimers in human frontal cortex and hippocampus
BMC Neuroscience volume 11, Article number: 23 (2010)
Apolipoprotein-E (apoE) plays important roles in neurobiology and the apoE4 isoform increases risk for Alzheimer's disease (AD). ApoE3 and apoE2 are known to form disulphide-linked dimers in plasma and cerebrospinal fluid whereas apoE4 cannot form these dimers as it lacks a cysteine residue. Previous in vitro research indicates dimerisation of apoE3 has a significant impact on its functions related to cholesterol homeostasis and amyloid-beta peptide degradation. The possible occurrence of apoE dimers in cortical tissues has not been examined and was therefore assessed. Human frontal cortex and hippocampus from control and AD post-mortem samples were homogenised and analysed for apoE by western blotting under both reducing and non-reducing conditions.
In apoE3 homozygous samples, ~12% of apoE was present as a homodimer and ~2% was detected as a 43 kDa heterodimer. The level of dimerisation was not significantly different when control and AD samples were compared. As expected, these dimerised forms of apoE were not detected in apoE4 homozygous samples but were detected in apoE3/4 heterozygotes at a level approximately 60% lower than seen in the apoE3 homozygous samples. Similar apoE3 dimers were also detected in lysates of SK-N-SH neuroblastoma cells and in freshly prepared rabbit brain homogenates. The addition of the thiol trapping agent, iodoacetamide, to block reactive thiols during both human and rabbit brain sample homogenisation and processing did not reduce the amount of apoE homodimer recovered. These data indicate that the apoE dimers we detected in the human brain are not likely to be post-mortem artefacts.
The identification of disulphide-linked apoE dimers in human cortical and hippocampal tissues represents a distinct structural difference between the apoE3 and apoE4 isoforms that may have functional consequences.
Apolipoprotein-E (apoE) is a ~34 kDa protein that plays important roles in lipid transport and neurobiology [1, 2]. In humans, apoE exists as three major isoforms apoE2, apoE3 and apoE4 which differ in their Cys/Arg composition at positions 112 and 158. ApoE2 contains Cys112, Cys158; apoE3 contains Cys112, Arg158; and apoE4 contains Arg112, Arg158. ApoE4 is a major genetic risk factor for late-onset Alzheimer's disease (AD) whereas apoE2 is associated with decreased AD risk [4, 5]. ApoE in the CNS is primarily produced by astrocytes, although microglia and neurons may also contribute under certain circumstances [1, 6–8, 8–11].
ApoE participates in several biological processes that extend beyond lipid transport and include immunoregulation, oxidative stress, stabilization of neuronal microtubules, nerve regeneration, apoptosis and amyloid-beta (Aβ) peptide clearance and degradation [11–20]. Despite intense research into the diverse biological functions of apoE, the precise mechanism by which the apoE4 isoform increases AD risk remains to be fully elucidated. However, many differences between apoE3 and apoE4 structure and function have been reported that are potentially relevant to AD. These include: reduced lipid-binding capacity of apoE4 due to isoform-specific domain interactions , lipidated apoE4 has a lower affinity for Aβ [22, 23], apoE4 is less efficient at stabilizing microtubules , apoE4 exhibits weaker antioxidant activity  and apoE4 is structurally less stable [24, 25] when compared to apoE3. It is also clear that the proteolytic fragmentation of apoE in the human brain is isoform-dependent [26–29]. In addition, a significant proportion of apoE3 (and apoE2) is present in plasma, CSF and astrocyte conditioned media as a disulfide-linked homodimer and as an apoE-apoA-II heterodimer [30–34]. This may be important as apoE4 lacks Cys and cannot form disulphide-linked dimers. In vitro studies have shown that compared to apoE monomers, apoE dimers possess significantly altered functional properties in terms of their capacity to regulate cellular cholesterol efflux and to interact with Aβ [30, 35–38]. This further underscores the importance of probing for the possible occurrence of apoE dimers in the human brain. In the present study we demonstrate that disulphide-linked apoE homodimers and heterodimers are present in the human cortex and hippocampus. In addition, we show that apoE dimerisation was not affected by the presence of AD.
ApoE3 forms disulfide-linked dimers in the human brain
It is established that apoE3 forms disulphide-linked homodimers and apoE3-apoA-II heterodimers in human plasma and CSF [30, 33]. As apoE4 lacks Cys it cannot form disulphide bonds. Whether apoE3 exists in a dimeric state in human brain tissue is unknown and we therefore focused on this issue. Western blot analysis of TBS-soluble brain homogenates derived from the hippocampus of a control apoE3/3 subject indicated a clear apoE3 homodimer when the sample was run under non-reducing conditions (Fig 1A). The homodimer was detected at ~95 kDa (as opposed to the predicted ~68 kDa) which is consistent with previous data [30, 33]. ApoE contains a major cut site for thrombin in the linker region . Due to the high proteolytic specificity of thrombin [40, 41], it was used here to further confirm the identification of the ~95 kDa band as an apoE homodimer. The putative apoE3 homodimer was removed after incubation with thrombin, as predicted, further confirming that the ~95 kDa band is not likely to be due to non-specific binding of the antibody used.
Incubation of the homogenate in the presence of heat-inactivated thrombin resulted in a partial loss of the apoE dimer which suggests that endogenous proteases may also degrade apoE (Fig 1A). A band of relatively lower intensity was also observed at ~43 kDa in the non-incubated apoE3 control condition. This is consistent with the apoE-apoA-II heterodimer previously detected in human plasma and CSF [30, 33]. A series of apoE fragments was also detected with a major band at ~24 kDa. This is in close agreement to our previous observations .
Additional hippocampal and frontal cortex homogenates from control apoE3/3 donors were analysed and this revealed that the apoE3 homodimer was present in all samples and accounted for 8.3 ± 0.9% (mean ± SE, n = 6) of the total apoE present in the hippocampus and 16.5% ± 4.1% (mean ± SE, n = 7) of the total apoE present in the frontal cortex (Fig 2). Although the percentage of apoE present as the homodimer was on average increased in the frontal cortex, this difference did not reach statistical significance. We also analysed frontal cortex and hippocampus derived from apoE3/3 AD samples and found that apoE3 dimers were detected in all AD samples and were identical to those in the control samples (Fig 1B). There was no significant difference regarding the proportion of apoE that was present in the dimerised form when frontal cortex from the two groups were compared (Control 16.5 ± 4.1%, mean ± SE, n = 7; AD 11.2 ± 2.4%, mean ± SE, n = 5).
We also used an additional rigorous extraction protocol employing extraction buffer that contained the detergent Triton-X100. This was done in order to maximise recovery of apoE that may be associated with TBS-insoluble material. Both the control and AD samples were found to contain apoE homodimers when samples were extracted in detergent-containing buffer (Fig 3). These data are very similar to the results obtained with the TBS-soluble homogenates (Fig 1).
As predicted, apoE dimers were not detected in any of the 7 apoE4/4 AD samples analyzed (Fig 4, see also Fig 1C). Analysis of heterozygous apoE3/4 AD samples revealed a significant 61% reduction in the percentage of apoE3 present as homodimer as compared to apoE3/3 homozygous AD samples (AD 3/3 11.2 ± 2.4%, mean ± SE, n = 5; AD 3/4 4.4% ± 0.6, mean ± SE, n = 5; p < 0.03). Representative blots from heterozygous apoE3/4 AD samples are shown (Fig 5).
ApoE3 forms disulphide-linked dimers in human SK-N-SH neurons and rabbit brain
One potential issue that arises in the analysis of protein modifications in human post-mortem material is the potential for artifactual changes to be induced by post-mortem interval (PMI). Even though clear ~95 kDa and ~43 kDa apoE dimers were detected in apoE3 AD homozygous samples with a post-mortem delay of as short as 1 h (and PMI for the AD sample shown in Fig 1B was only 7 h), we also probed for apoE dimers in human neuroblastoma cell lysates and freshly harvested rabbit brain. The human SK-N-SH neuroblastoma cell line expresses the APOE ε3/ε3 genotype [42, 43] and synthesizes large amounts of apoE under serum starved conditions , whereas rabbits are one of the few non-human species known to contain an apoE Cys112 residue .
Analysis of SK-N-SH cell lysates under non-reducing conditions revealed the presence of the ~95 kDa apoE homodimer and a more prominent (than human brain) ~43 kDa heterodimer (Fig 6A). Since the ~43 kDa dimer could theoretically represent a disulphide-linked apoE N-terminal domain homodimer (a predicted MW of ~44 kDa), we used a C-terminal specific monoclonal antibody in this experiment and the detection of the ~43 kDa band indicates an intact C-terminus. This rules out the presence of disulphide-linked N-terminal domain homodimer. The ~43 kDa band may represent an apoE3-apoA-II heterodimer as has been previously described in human plasma and CSF [30, 33].
In the analysis of rabbit frontal cortex, the brain was dissected and processed immediately at the time of death to eliminate post-mortem delay and all measures were taken to prevent serum and CSF contamination (see Materials and Methods). An apoE band at ~95 kDa was also detected in rabbit brain when samples were run in the non-reduced state (Fig 6B), again indicating that apoE containing Cys112 does form a homodimer in the brain.
To address the possibility that the observed apoE dimerisation may occur during tissue homogenization and processing for electrophoresis, freshly prepared rabbit brain and frozen human frontal cortex tissue (AD apoE3/3) were homogenized in buffer containing the thiol trapping agent iodoacetamide. Homogenization was also performed using a detergent-rich lysis buffer to delipidate apoE-containing lipoproteins and help prevent the possibility of dimers forming spontaneously on lipoprotein particles during homogenization and processing. The presence of 100 mM iodoacetamide did not result in a decrease in apoE homodimer levels in either rabbit or human brain tissue (Fig 7A). The thiol-trapping efficiency of 100 mM iodoacetamide was confirmed by spectrophotometric analysis of the total thiol concentration of the homogenates using Ellman's reagent (5,5'-Dithio-bis(2-nitrobenzoic acid)). The total thiol concentration was significantly reduced in both rabbit and human brain homogenates (84% and 96%, respectively) treated with iodoacetamide (Fig 7B). This data demonstrates that apoE dimers are not artificially formed during tissue homogenization and processing, and further indicates that apoE dimers are generated in the brain.
This study demonstrates for the first time that apoE3 disulphide-linked dimers are present in human frontal cortex and hippocampus. Furthermore, strikingly similar dimers were also detected in human neuroblastoma cells expressing apoE3 and in freshly prepared rabbit brain. These data indicate that apoE3 dimerisation is a physiologically relevant process in the human brain; as it is in human CSF and plasma [30, 33]. The biological functions of these apoE dimers in the brain is not yet clear, however, several studies support the possibility that they may have distinct properties that differ from apoE monomer. Previous studies have demonstrated that apoE3 homodimers and apoE3-apoA-II heterodimers have diminished low-density lipoprotein receptor binding activity (20% and 30%, respectively) in comparison to apoE3 monomer [30, 35]. In vitro studies have shown that the apoE-apoA-II dimer is more effective than apoE monomer in binding soluble Aβ1-42 and inhibiting its internalisation by neurons [36, 37]. In addition, a recent study has demonstrated that the apoE3 homodimer is more effective than monomeric apoE3 at enhancing ABCA1-dependent lipid efflux from neurons .
Based on these data, it seems possible that the reported physiological properties of apoE dimers may enhance some of the AD-protective functions attributed to apoE3. For example, the role of apoE in Aβ clearance and degradation [18, 20] may be facilitated by enhanced binding with Aβ1-42 . In addition, the enhanced neuronal cholesterol efflux that is induced by apoE dimers as compared to monomers  may be important considering that high levels of neuronal cholesterol can influence processing of the amyloid precursor protein and increase Aβ production [44–47]. Thus dimerisation may represent one mechanism by which apoE3 and apoE2 have a distinct AD-protective advantage over apoE4. However, this feature alone is probably not the crucial regulator underlying apoE genotype-associated risk as the dimers were detectable at similar levels in apoE3 homozygous control and AD samples.
In conclusion, the presence of apoE3 dimers in the human brain represents a fundamental structural difference between apoE3 and apoE4. A greater understanding of the biological consequences of this difference may shed light on the isoform-dependent influences of apoE on AD risk.
Human brain tissue
Brain tissue samples were obtained through the Australian Brain Donor Program with ethics approval from the University of New South Wales Human Research Ethics Committee (approval No. HREC03322). The research was carried out in compliance with the Helsinki Declaration. Cortical neuritic plaques and neurofibrillary tangles were assessed according to current international standards in order to pathologically confirm the diagnosis of AD post-mortem [48, 49]. Sample details are provided in Table 1.
Human tissue preparation
Samples were taken from the frontal cortex or hippocampus; both areas that are affected by AD . The homogenisation protocol was previously described in detail , and was used for all samples unless stated otherwise. In brief, between 60-90 mg of brain tissue was homogenized with a pre-chilled 1 mL glass dounce homogenizer, using 15 volumes of ice-cold tris-buffered saline (TBS) pH 7.4. Protease and phosphatase inhibitors (Calbiochem, San Diego, USA) were added to all samples except those to be used in experiments requiring enzyme addition (samples C6, AD5 and AD6). After centrifugation at 16,000 g for 25 minutes at 4°C the TBS-soluble supernatant fraction was collected. Where specified, the pellet was then washed with 50 μL of TBS and centrifuged again for 5 min, the supernatant was then discarded and pellet was resuspended in 15 volumes of TBS containing protease and phosphatase inhibitors and 1% (w/v) Triton X-100 (TBS-X) by pipetting up and down. Samples were then mixed by rotation for 30 min at 4°C, followed by centrifugation at 16,000 g for 25 min at 4°C and collection of the TBS-X soluble supernatant fraction.
A second protocol was also used, where specified, to homogenise brain tissue in a detergent-rich lysis buffer. In brief, brain tissue was homogenized with a pre-chilled 1 mL glass dounce homogenizer, using 10 volumes of DRLB (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 0.1% SDS, 0.5% IGEPAL CA-630, 0.5% sodium deoxycholate) with protease and phosphatase inhibitors and either with or without 100 mM iodoacetamide (Sigma) to trap thiol groups and thus prevent changes in disulphide bond status during homogenization and sample processing . Homogenates were then centrifuged at 16,000 g for 10 min at 4°C in an Eppendorf 5417-R refrigerated Microfuge and the supernatants collected.
Rabbit tissue preparation
An adult male Watanabe rabbit was euthanased via cardiac puncture using 5 mL Lethabarb (1 mL per 2 kg body weight, Virbac, Sydney, Australia) and the brain surgically removed to dry ice and processed immediately in order to eliminate post-mortem delay. Approximately 100 mg of tissue was removed from the cerebral cortex, all visible vasculature was removed and the sample was rinsed three times in ice-cold phosphate-buffered saline (PBS). The sample was then homogenized following the protocol used above for the human samples.
Genomic DNA was extracted from brain tissue and APOE amplified by PCR. Briefly, each reaction (50 μL) contained 200 nM of each primer (Invitrogen, Carlsbad, CA) 5'-TCCAAGGAGCTGCAGGCGGCGCA-3' (forward) and 5'-ACAGAATTCGCCCCGGCCTGGTACACTGCCA-3' (reverse), 2 mM dNTPs, 2 mM MgCl2, 2 U Taq polymerase (PCR reagents supplied by Promega, Madison, WI) and 400 ng DNA, all combined in nuclease free H2O. Amplification was carried out with 38 cycles of denaturation (95°C, 30 sec), annealing (60°C, 30 sec) and extension (70°C, 30 sec). The 244 bp PCR product was purified using the QIAquick PCR purification kit (Qiagen, Venlo, Netherlands), following the manufacturer's protocol, and eluted in 40 μL H2O. Endonuclease restriction digests (25 μL) were performed on 15 μL of eluted DNA using either AflIII (5 U) or HaeII (20 U) in the presence of BSA (100 μg/mL) and the supplied buffer (New England Biolabs, Ipswich, MA) at 37°C for 16 h. The ε3 allele is resistant to both enzymes while ε4 is cleaved by AflIII (producing a 190 bp product) and ε2 is cleaved by HaeII (producing a 191 bp product) assessed using ethidium bromide stained 8% polyacrylamide gels.
SK-N-SH neuroblastoma cell culture
Cell culture media and additives were from Invitrogen (Melbourne, Australia). Human neuronal SK-N-SH cells were routinely grown in DMEM, 10% (v/v) fetal calf serum (FCS), 2 mM glutamine, and 100 IU/ml penicillin and 100 μg/ml streptomycin. Cultures were grown in 75 cm2 flasks at 37°C in 5% CO2 and plated into 6-well plates for use in experiments. To induce apoE expression, SK-N-SH cells were cultured under serum starved conditions (5 days of culture without media replenishment) and harvested in cell lysis buffer (10 mM Tris-HCl, 10 mM Na2PO4/NaHPO4, pH 7.5, 130 mM NaCl, 1% Triton-X-100, 10 mM NaPPi) as described previously . SK-N-SH cells have been shown to be apoE3/3 homozygous [42, 43].
Bicinchoninic acid protein assays were performed on brain homogenate samples and equal amounts of protein were separated on 12% SDS-PAGE gels and transferred onto 0.45 μm nitrocellulose membranes at 100 V for 30 min. Membranes were Ponceau-stained and scanned before blocking overnight at 4°C in PBS containing 5% (w/v) non-fat dry milk. The membranes were then probed with the relevant antibodies at 22°C for 1 h to reveal the bands of interest. Concentrations of antibodies were: goat polyclonal anti-human apoE 1/5000 (Calbiochem) or mouse monoclonal anti-human apoE 21-F3-D2 1/1000 (Biogenesis, Poole, UK). The membranes were washed three times in PBS containing 0.1% (w/v) Tween-20 and then incubated with horseradish peroxidase-conjugated rabbit anti-goat (Dako, 1/2500) or rabbit anti-mouse (Dako, 1/1000) secondary antibody for 1 h. The proteins of interest were detected using enhanced chemiluminescence (ECL, Amersham Biosciences) and X-ray film. Signal intensity was quantified using Image-J software. Specifically, a fixed area was used to separately measure signal intensity from i) the region encompassing intact ~34 kDa and fragmented ~24 kDa apoE, ii) apoE homodimer at ~95 kDa, and iii) an adjacent blank region to serve as a background control. The background value (iii) was subtracted from the apoE measurements (i and ii) and the homodimer quantification was expressed as a percentage of total apoE. Where possible, relative differences between samples were assessed on the same blots or using simultaneously processed gels with identical film exposure times.
Enzymatic treatment of brain homogenates
Thrombin digestion was performed by incubating brain homogenates (30 μg of protein) prepared in the absence of protease inhibitors with 4.5 U of thrombin (Sigma, St. Louis, MO) in PBS at 37°C for 16 hours. Two control conditions were also analysed: homogenates either stored at -80°C for the incubation period or incubated with thrombin that was heat-inactivated at 95°C for 15 minutes.
The concentration of total thiol groups, both protein-bound and free, in specified brain homogenates was determined using 5,5'-dithio-bis(2-nitrobenzoic acid) (DTNB, Sigma) also known as 'Ellman's Reagent' as described previously . Briefly, a 30 μL volume of brain homogenate (either undiluted or diluted in homogenisation buffer) was combined with 75 μL of dilution buffer (30 mM Tris HCl, 3 mM EDTA pH 8.2), 25 μL of DTNB reagent (1.19 mg/mL DTNB in methanol) and 400 μL methanol. Samples were centrifuged at 3000 g for 5 min at room temperature. 3 × 90 μL aliquots of supernatant were collected and absorbance was measured at 415 nm. Thiol concentration was determined by reference to a cysteine (Sigma) standard curve.
central nervous system
polyacrylamide gel electrophoresis
phosphate buffered saline
sodium dodecyl sulfate
tris buffered saline
TBS containing 1% (w/v) Triton X-100
Mahley RW: Apolipoprotein E: cholesterol transport protein with expanding role in cell biology. Science. 1988, 240: 622-630. 10.1126/science.3283935.
Ladu MJ, Reardon C, Van Eldik L, Fagan AM, Bu G, Holtzman D, Getz GS: Lipoproteins in the central nervous system. Ann N Y Acad Sci. 2000, 903: 167-175. 10.1111/j.1749-6632.2000.tb06365.x.
Rall SC, Weisgraber KH, Innerarity TL, Mahley RW: Structural basis for receptor binding heterogeneity of apolipoprotein E from type III hyperlipoproteinemic subjects. Proc Natl Acad Sci USA. 1982, 79: 4696-4700. 10.1073/pnas.79.15.4696.
Corder EH, Saunders AM, Strittmatter WJ, Schmechel DE, Gaskell PC, Small GW, Roses AD, Haines JL, Pericak-Vance MA: Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 1993, 261: 921-923. 10.1126/science.8346443.
Strittmatter WJ, Saunders AM, Schmechel D, Pericak-Vance M, Enghild J, Salvesen GS, Roses AD: Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease. Proc Natl Acad Sci USA. 1993, 90: 1977-1981. 10.1073/pnas.90.5.1977.
LaDu MJ, Gilligan SM, Lukens JR, Cabana VG, Reardon CA, Van Eldik LJ, Holtzman DM: Nascent astrocyte particles differ from lipoproteins in CSF. J Neurochem. 1998, 70: 2070-2081.
Xu Q, Li Y, Cyras C, Sanan DA, Cordell B: Isolation and characterization of apolipoproteins from murine microglia. Identification of a low density lipoprotein-like apolipoprotein J-rich but E-poor spherical particle. J Biol Chem. 2000, 275: 31770-31777. 10.1074/jbc.M002796200.
Xu PT, Gilbert JR, Qiu HL, Ervin J, Rothrock-Christian TR, Hulette C, Schmechel DE: Specific regional transcription of apolipoprotein E in human brain neurons. Am J Pathol. 1999, 154: 601-611.
Boschert U, Merlo-Pich E, Higgins G, Roses AD, Catsicas S: Apolipoprotein E expression by neurons surviving excitotoxic stress. Neurobiol Dis. 1999, 6: 508-514. 10.1006/nbdi.1999.0251.
Metzger RE, LaDu MJ, Pan JB, Getz GS, Frail DE, Falduto MT: Neurons of the human frontal cortex display apolipoprotein E immunoreactivity: implications for Alzheimer's disease. J Neuropathol Exp Neurol. 1996, 55: 372-380. 10.1097/00005072-199603000-00013.
Elliott DA, Kim WS, Jans DA, Garner B: Apoptosis induces neuronal apolipoprotein-E synthesis and localization in apoptotic bodies. Neurosci Lett. 2007, 416: 206-210. 10.1016/j.neulet.2007.02.014.
Mahley RW, Nathan BP, Pitas RE: Apolipoprotein E. Structure, function, and possible roles in Alzheimer's disease. Ann N Y Acad Sci. 1996, 777: 139-145. 10.1111/j.1749-6632.1996.tb34412.x.
Miyata M, Smith JD: Apolipoprotein E allele-specific antioxidant activity and effects on cytotoxicity by oxidative insults and beta-amyloid peptides. Nat Genet. 1996, 14: 55-61. 10.1038/ng0996-55.
Strittmatter WJ, Weisgraber KH, Goedert M, Saunders AM, Huang D, Corder EH, Dong LM, Jakes R, Alberts MJ, Gilbert JR, et al.: Hypothesis: microtubule instability and paired helical filament formation in the Alzheimer disease brain are related to apolipoprotein E genotype. Exp Neurol. 1994, 125: 163-171. 10.1006/exnr.1994.1019. discussion 172-164
Mahley RW, Rall SC: Apolipoprotein E: far more than a lipid transport protein. Annu Rev Genomics Hum Genet. 2000, 1: 507-537. 10.1146/annurev.genom.1.1.507.
Arai H, Kashiwagi S, Nagasaka Y, Uchida K, Hoshii Y, Nakamura K: Oxidative modification of apolipoprotein E in human very-low-density lipoprotein and its inhibition by glycosaminoglycans. Arch Biochem Biophys. 1999, 367: 1-8. 10.1006/abbi.1999.1222.
Jordan J, Galindo MF, Miller RJ, Reardon CA, Getz GS, LaDu MJ: Isoform-specific effect of apolipoprotein E on cell survival and beta-amyloid-induced toxicity in rat hippocampal pyramidal neuronal cultures. J Neurosci. 1998, 18: 195-204.
Beffert U, Aumont N, Dea D, Lussier-Cacan S, Davignon J, Poirier J: Apolipoprotein E isoform-specific reduction of extracellular amyloid in neuronal cultures. Brain Res Mol Brain Res. 1999, 68: 181-185. 10.1016/S0169-328X(99)00073-X.
Bell RD, Sagare AP, Friedman AE, Bedi GS, Holtzman DM, Deane R, Zlokovic BV: Transport pathways for clearance of human Alzheimer's amyloid beta-peptide and apolipoproteins E and J in the mouse central nervous system. J Cereb Blood Flow Metab. 2007, 27: 909-918.
Jiang Q, Lee CY, Mandrekar S, Wilkinson B, Cramer P, Zelcer N, Mann K, Lamb B, Willson TM, Collins JL, et al.: ApoE promotes the proteolytic degradation of Abeta. Neuron. 2008, 58: 681-693. 10.1016/j.neuron.2008.04.010.
Xu Q, Brecht WJ, Weisgraber KH, Mahley RW, Huang Y: Apolipoprotein E4 domain interaction occurs in living neuronal cells as determined by fluorescence resonance energy transfer. J Biol Chem. 2004, 279: 25511-25516. 10.1074/jbc.M311256200.
LaDu MJ, Falduto MT, Manelli AM, Reardon CA, Getz GS, Frail DE: Isoform-specific binding of apolipoprotein E to beta-amyloid. J Biol Chem. 1994, 269: 23403-23406.
Tokuda T, Calero M, Matsubara E, Vidal R, Kumar A, Permanne B, Zlokovic B, Smith JD, Ladu MJ, Rostagno A: Lipidation of apolipoprotein E influences its isoform-specific interaction with Alzheimer's amyloid beta peptides. Biochem J. 2000, 348 (Pt 2): 359-365. 10.1042/0264-6021:3480359.
Morrow JA, Segall ML, Lund-Katz S, Phillips MC, Knapp M, Rupp B, Weisgraber KH: Differences in stability among the human apolipoprotein E isoforms determined by the amino-terminal domain. Biochemistry. 2000, 39: 11657-11666. 10.1021/bi000099m.
Clement-Collin V, Barbier A, Dergunov AD, Visvikis A, Siest G, Desmadril M, Takahashi M, Aggerbeck LP: The structure of human apolipoprotein E2, E3 and E4 in solution. 2. Multidomain organization correlates with the stability of apoE structure. Biophys Chem. 2006, 119: 170-185. 10.1016/j.bpc.2005.07.009.
Marques MA, Tolar M, Harmony JA, Crutcher KA: A thrombin cleavage fragment of apolipoprotein E exhibits isoform-specific neurotoxicity. Neuroreport. 1996, 7: 2529-2532. 10.1097/00001756-199611040-00025.
Tolar M, Marques MA, Harmony JA, Crutcher KA: Neurotoxicity of the 22 kDa thrombin-cleavage fragment of apolipoprotein E and related synthetic peptides is receptor-mediated. J Neurosci. 1997, 17: 5678-5686.
Huang Y, Liu XQ, Wyss-Coray T, Brecht WJ, Sanan DA, Mahley RW: Apolipoprotein E fragments present in Alzheimer's disease brains induce neurofibrillary tangle-like intracellular inclusions in neurons. Proc Natl Acad Sci USA. 2001, 98: 8838-8843. 10.1073/pnas.151254698.
Elliott DA, Tsoi K, Holinkova S, Chan SL, Kim WS, Halliday GM, Rye KA, Garner B: Isoform-specific proteolysis of apolipoprotein-E in the brain. Neurobiol Aging. 2010.
Weisgraber KH, Shinto LH: Identification of the disulfide-linked homodimer of apolipoprotein E3 in plasma. Impact on receptor binding activity. J Biol Chem. 1991, 266: 12029-12034.
LaDu MJ, Lukens JR, Reardon CA, Getz GS: Association of human, rat, and rabbit apolipoprotein E with beta-amyloid. J Neurosci Res. 1997, 49: 9-18. 10.1002/(SICI)1097-4547(19970701)49:1<9::AID-JNR2>3.0.CO;2-H.
Montine KS, Bassett CN, Ou JJ, Markesbery WR, Swift LL, Montine TJ: Apolipoprotein E allelic influence on human cerebrospinal fluid apolipoproteins. J Lipid Res. 1998, 39: 2443-2451.
Rebeck GW, Alonzo NC, Berezovska O, Harr SD, Knowles RB, Growdon JH, Hyman BT, Mendez AJ: Structure and functions of human cerebrospinal fluid lipoproteins from individuals of different APOE genotypes. Exp Neurol. 1998, 149: 175-182. 10.1006/exnr.1997.6710.
Sun Y, Wu S, Bu G, Onifade MK, Patel SN, LaDu MJ, Fagan AM, Holtzman DM: Glial fibrillary acidic protein-apolipoprotein E (apoE) transgenic mice: astrocyte-specific expression and differing biological effects of astrocyte-secreted apoE3 and apoE4 lipoproteins. J Neurosci. 1998, 18: 3261-3272.
Innerarity TL, Mahley RW, Weisgraber KH, Bersot TP: Apoprotein (E-A-II) complex of human plasma lipoproteins. II. Receptor binding activity of a high density lipoprotein subfraction modulated by the apo(E--A-II) complex. J Biol Chem. 1978, 253: 6289-6295.
Yamauchi K, Tozuka M, Hidaka H, Nakabayashi T, Sugano M, Kondo Y, Nakagawara A, Katsuyama T: Effect of apolipoprotein AII on the interaction of apolipoprotein E with beta-amyloid: some apo(E-AII) complexes inhibit the internalization of beta-amyloid in cultures of neuroblastoma cells. J Neurosci Res. 2000, 62: 608-614. 10.1002/1097-4547(20001115)62:4<608::AID-JNR16>3.0.CO;2-4.
Yamauchi K, Tozuka M, Nakabayashi T, Sugano M, Hidaka H, Kondo Y, Katsuyama T: Higher avidity binding of apolipoprotein (E-AII) complex than of apolipoprotein E monomer to beta-amyloid. J Neurosci Res. 1999, 58: 301-307. 10.1002/(SICI)1097-4547(19991015)58:2<301::AID-JNR10>3.0.CO;2-9.
Minagawa H, Gong JS, Jung CG, Watanabe A, Lund-Katz S, Phillips MC, Saito H, Michikawa M: Mechanism underlying apolipoprotein E (ApoE) isoform-dependent lipid efflux from neural cells in culture. J Neurosci Res. 2009, 87: 2498-2508. 10.1002/jnr.22073.
Bradley WA, Gilliam EB, Gotto AM, Gianturco SH: Apolipoprotein-E degradation in human very low density lipoproteins by plasma protease(s): chemical and biological consequences. Biochem Biophys Res Commun. 1982, 109: 1360-1367. 10.1016/0006-291X(82)91927-1.
Bode W: Structure and interaction modes of thrombin. Blood Cells Mol Dis. 2006, 36: 122-130. 10.1016/j.bcmd.2005.12.027.
Huntington JA: Molecular recognition mechanisms of thrombin. J Thromb Haemost. 2005, 3: 1861-1872. 10.1111/j.1538-7836.2005.01363.x.
Caillet-Boudin ML, Dupont-Wallois L, Soulie C, Delacourte A: Apolipoprotein E and Tau phosphorylation in human neuroblastoma cells. Neurosci Lett. 1998, 250: 83-86. 10.1016/S0304-3940(98)00448-0.
Dupont-Wallois L, Soulie C, Sergeant N, Wavrant-de Wrieze N, Chartier-Harlin MC, Delacourte A, Caillet-Boudin ML: ApoE synthesis in human neuroblastoma cells. Neurobiol Dis. 1997, 4: 356-364. 10.1006/nbdi.1997.0155.
Simons M, Keller P, De Strooper B, Beyreuther K, Dotti CG, Simons K: Cholesterol depletion inhibits the generation of beta-amyloid in hippocampal neurons. Proc Natl Acad Sci USA. 1998, 95: 6460-6464. 10.1073/pnas.95.11.6460.
Runz H, Rietdorf J, Tomic I, de Bernard M, Beyreuther K, Pepperkok R, Hartmann T: Inhibition of intracellular cholesterol transport alters presenilin localization and amyloid precursor protein processing in neuronal cells. J Neurosci. 2002, 22: 1679-1689.
Kim WS, Suryo Rahmanto A, Kamili A, Rye KA, Guillemin GJ, Gelissen IC, Jessup W, Hill AF, Garner B: Role of ABCG1 and ABCA1 in regulation of neuronal cholesterol efflux to apolipoprotein-E discs and suppression of amyloid-beta peptide generation. J Biol Chem. 2007, 282: 2851-2861. 10.1074/jbc.M607831200.
Kim WS, Weickert CS, Garner B: Role of ATP-binding cassette transporters in brain lipid transport and neurological disease. J Neurochem. 2008, 104: 1145-1166. 10.1111/j.1471-4159.2007.05099.x.
Mirra SS, Heyman A, McKeel D, Sumi SM, Crain BJ, Brownlee LM, Vogel FS, Hughes JP, van Belle G, Berg L: The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology. 1991, 41: 479-486.
NIA: Consensus recommendations for the postmortem diagnosis of Alzheimer's disease. The National Institute on Aging, and Reagan Institute Working Group on Diagnostic Criteria for the Neuropathological Assessment of Alzheimer's Disease. Neurobiol Aging. 1997, 18: S1-2. 10.1016/S0197-4580(97)00057-2.
West MJ, Coleman PD, Flood DG, Troncoso JC: Differences in the pattern of hippocampal neuronal loss in normal ageing and Alzheimer's disease. Lancet. 1994, 344: 769-772. 10.1016/S0140-6736(94)92338-8.
Furukawa Y, Fu R, Deng HX, Siddique T, O'Halloran TV: Disulfide cross-linked protein represents a significant fraction of ALS-associated Cu, Zn-superoxide dismutase aggregates in spinal cords of model mice. Proc Natl Acad Sci USA. 2006, 103: 7148-7153. 10.1073/pnas.0602048103.
Ellman GL: Tissue sulfhydryl groups. Arch Biochem Biophys. 1959, 82: 70-77. 10.1016/0003-9861(59)90090-6.
Human brain tissue samples were received from the Australian Brain Donor Program, Prince of Wales Medical Research Institute Brain Bank, which is supported by the Australian National Health and Medical Research Council (NHMRC). This work was supported by a Viertel Foundation Postdoctoral Fellowship in Dementia awarded to DE by Alzheimer's Australia. GH and BG are supported by Fellowships from the NHMRC and the Australian Research Council.
DE carried out the experimental work, performed the statistical analysis and drafted the manuscript. GH collected and provided human brain tissues. BG conceived of the study, participated in its design and coordination and prepared the final manuscript. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Elliott, D.A., Halliday, G.M. & Garner, B. Apolipoprotein-E forms dimers in human frontal cortex and hippocampus. BMC Neurosci 11, 23 (2010). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2202-11-23
- Brain Homogenate
- Rabbit Brain
- Human Frontal Cortex
- Total apoE
- Total Thiol Concentration