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(American Journal of Pathology. 2004;165:937-948.)
© 2004 American Society for Investigative Pathology

A Synthetic Peptide Blocking the Apolipoprotein E/ß-Amyloid Binding Mitigates ß-Amyloid Toxicity and Fibril Formation in Vitro and Reduces ß-Amyloid Plaques in Transgenic Mice

Marcin Sadowski*, Joanna Pankiewicz*, Henrieta Scholtzova*, James A. Ripellino*, Yongsheng Li*, Stephen D. Schmidt{dagger}, Paul M. Mathews{dagger}, John D. Fryer{ddagger}, David M. Holtzman{ddagger}, Einar M. Sigurdsson§ and Thomas Wisniewski*§

From the Departments of Neurology,* Psychiatry§ and Pathology, New York University School of Medicine, New York, New York; Nathan S. Kline Institute,{dagger} New York University, Orangeburg, New York; and the Departments of Neurology, Molecular Biology, and Pharmacology,{ddagger} Center for the Study of Nervous System Injury, Washington University School of Medicine, St. Louis, Missouri


   Abstract
Top
 Abstract
Materials and Methods
 Results
 Discussion
 References
 
Alzheimer’s disease (AD) is associated with accumulation of ß-amyloid (Aß). A major genetic risk factor for sporadic AD is inheritance of the apolipoprotein (apo) E4 allele. ApoE can act as a pathological chaperone of Aß, promoting its conformational transformation from soluble Aß into toxic aggregates. We determined if blocking the apoE/Aß interaction reduces Aß load in transgenic (Tg) AD mice. The binding site of apoE on Aß corresponds to residues 12 to 28. To block binding, we synthesized a peptide containing these residues, but substituted valine at position 18 to proline (Aß12–28P). This changed the peptide’s properties, making it non-fibrillogenic and non-toxic. Aß12–28P competitively blocks binding of full-length Aß to apoE (IC50 = 36.7 nmol). Furthermore, Aß12–28P reduces Aß fibrillogenesis in the presence of apoE, and Aß/apoE toxicity in cell culture. Aß12–28P is blood-brain barrier-permeable and in AD Tg mice inhibits Aß deposition. Tg mice treated with Aß12–28P for 1 month had a 63.3% reduction in Aß load in the cortex (P = 0.0043) and a 59.5% (P = 0.0087) reduction in the hippocampus comparing to age-matched control Tg mice. Antibodies against Aß were not detected in sera of treated mice; therefore the observed therapeutic effect of Aß12–28P cannot be attributed to an antibody clearance response. Our experiments demonstrate that compounds blocking the interaction between Aß and its pathological chaperones may be beneficial for treatment of ß-amyloid deposition in AD.

A disturbance of amyloid-ß (Aß) homeostasis in Alzheimer’s disease (AD) leads to the accumulation of this peptide in the form of plaques in the brain.1 Increased production of Aß peptides or their inadequate clearance can lead to brain accumulation. It has been demonstrated that peptides homologous to Aß form amyloid fibrils in solution if they reach a critical concentration.2 This process can be effectively promoted by Aß pathological chaperone proteins (for review, see3 ) such as apolipoprotein E (apoE), especially its E4 isoform,4 {propto} 1-antichymotrypsin (ACT),5 or C1q complement factor.6 They promote formation of Aß fibrils, which remain sequestered within the brain and accumulate in the form of plaques.7 Inheritance of the apo E4 isoform has been identified as the major identified genetic risk factor for sporadic, late-onset AD8 and correlates with an earlier age of onset and greater Aß deposition, in an allele dose-dependent manner.8-10 ApoE is a 34-kd glycosylated protein existing in three major isoforms E2, E3, and E4, which differ in primary sequence at two residues. The chaperoning effect of apo E on the formation of Aß deposits has been studied in great detail. In vitro, all apo E isoforms can propagate the ß-sheet content of Aß peptides promoting fibril formation,11 with apo E4 being the most efficient.4 The dependence of Aß deposition in plaques on the presence of apoE has also been confirmed in vivo. Crossing APPV717F AD transgenic (Tg) mice onto an apoE knockout (KO) background resulted in a substantial reduction of the Aß load and an absence of fibrillar Aß deposits.12 Therefore, one can speculate that the selective ablation of apoE’s effect on Aß could potentially have a therapeutic effect leading to diminished Aß deposition and decreased Aß toxicity. ApoE hydrophobically binds Aß, forming SDS insoluble complexes.13-15 Although the affinity of binding depends on Aß conformation (Aß soluble versus fibrillar), it remains in the low nanomolar range.11,13,16,17 Prior studies have identified that residues 12–28 of Aß are the binding site for apoE on Aß.13,18 This sequence encompasses a hydrophobic domain (residues 14–21) and a ß-turn (residues 22–28) which place two hydrophobic domains of Aß (14–21 and 29–40/42) opposite each other allowing for assembly of Aß peptides into fibrils.19 Ma et al20 have demonstrated that a synthetic peptide homologous to 12–28 amino acid sequence of Aß can be used as a competitive inhibitor of the binding of full-length Aß to apo E, resulting in reduced fibril formation and increased survival of cultured neurons. These in vitro studies confirmed that the interaction of apoE with residues 12–28 of Aß is not just a non-specific hydrophobic interaction but plays a pivotal role in the mechanism of Aß pathology in AD. The goal of this study is to investigate whether compounds blocking the apoE/Aß interaction can be developed into a novel therapeutic approach for AD. Aß12–28 can be associated with toxicity, due to the 14 to 21 residue hydrophobic domain.21 It can also co-deposit on existing Aß plaques when injected into AD transgenic (Tg) mice.22 Therefore, we have modified the Aß12–28 sequence by substitution of the valine at residue 18 to proline, rendering this peptide non-fibrillogenic and non-toxic. Use of D-amino acids, amidation of the C-terminus, and acetylation of the N-terminus were designed to extend the serum half-life of the peptide, prolonging in vivo activity. In a series of experiments we analyzed the effect of pharmacological blockade of apo E’s pathological chaperoning properties on Aß fibrillogenesis and toxicity in vitro using Aß12–28 and Aß12–28P. Aß12–28P was also administered to AD Tg mice to investigate the in vivo effect of blocking the apoE/Aß interaction on Aß deposition.


   Materials and Methods
Top
 Abstract
 Materials and Methods
Results
 Discussion
 References
 
Synthetic Peptides and Proteins

Aß1–40, Aß1–42, Aß12–28, and Aß12–28P were synthesized in the W. M. Keck Facility at Yale University. Details of synthesis, purification, and sequence verification were described previously.23-25 Aß12–28P (VHHQKLPFFAEDVGSNK) was synthesized using D-amino acids and end protected by amidation of the C-terminus and acetylation of the N-terminus to minimize degradation by endogenous peptidases and extend the half-life. Aß12–28 (VHHQKLVFFAEDVGSNK) used in fibillization and tissue culture assays was also synthesized using D-amino acids to control for the racemic isomer effect. For aggregation studies and assessment of secondary structure, the peptides were treated with 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP; Sigma, St. Louis, MO) as described elsewhere.26 This treatment renders peptides monomeric with minimal ß-sheet content.

Recombinant apo E3 and apo E4, were purchased from Calbiochem Corp. (San Diego, CA). Lipidated apo E3 and apo E4 complexes were prepared from primary cultures of astrocytes derived from Tg mice in which human apo E3 or apo E4 were expressed under the control of the astrocyte-specific glial fibrillary acidic protein (GFAP) promoter as described previously.27-29 Briefly, primary cultures of forebrain astrocytes were maintained in serum-free Dulbecco’s modified Eagle’s medium/Ham’s F-12 (1:1) with N2 supplement (Invitrogen, Carlsbad, CA) for 72 hours. The medium was removed and clarified by centrifugation at 800 x g for 5 minutes and then concentrated by ultra-filtration. Human apoE was isolated by immunoaffinity chromatography. The purity of the apoE preparation was assessed by SDS-PAGE.28

Circular Dichroism Studies of Secondary Structure

Aliquots of HFIP-treated peptides were reconstituted in 5 mmol/L Tris buffer (pH 7.0) to obtain a peptide concentration of 100 µmol/L and were incubated at 37°C. Circular dichroism (CD) was measured at indicated intervals with t = 0 being immediately after the peptide was reconstituted on a Jasco J-720 spectropolarimeter (Jasco, Inc., Easton, MD) equipped with a model CTC-344 circular temperature control system (Neslab Inc., Newington, NH) according to our previously described protocols.11,30,31 The Lincomb, convex constraints and neural network algorithms (Softsec software; Softwood Inc., Scranton, PA) were used to obtain percentages of different types of secondary structures of analyzed peptides.32-35

Aggregation and Fluorometric Experiments

All peptides were incubated alone at concentrations 100 µmol/L over a period of 10 days at 37°C in 100 mmol/L Tris buffer (pH 7.4). Aß1–42 was also incubated in the presence of 1µmol/L of lipidated apo E3 or E4 (100:1 molar ratio). In aggregation inhibition experiments, apo E3 or E4 was preincubated with Aß12–28P in a molar ratio of 1:2 for 6 hours at 37°C and then added to freshly reconstituted Aß1–42. Aß1–42 was incubated with Aß12–28P at a molar ratio of 100:2 as a control. Amount of fibrils formed by the different peptides at different time points was evaluated by a Thioflavin-T assay on a Perkin-Elmer LS-50B fluorescence spectrophotometer (Perkin Elmer Instruments, Shelton, CT) according to previously published methods.4,11 The mean ± SD (SD) for three separate experiments was plotted in Figure 1 . Statistical analysis was performed by means of a repeated measures analysis of variance followed by a Tukey HSD post-hoc test using CSS Statistica (version 6.1, StatSoft Inc.; OK).



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  		Figure 1. A: Thioflavin-T assay demonstrates the modest ability of Aß12–28 to form fibrils which is significantly lower than Aß1–40 and Aß1–42 (P < 0.0001, repeated measures analysis of variance; P < 0.001 Aß12–28 versus Aß1–40 and Aß12–28 versus Aß1–42 Tukey HSD post-hoc test). No fibrils were formed by Aß12–28P. B: Aß1–42 was incubated in the presence of either apo E3 or apo E4 (solid red and blue lines) that significantly increased amount of fibrils formed over time compared with Aß1–42 alone (green line; P < 0.0001, repeated measures analysis of variance; P < 0.01 and P < 0.05 Tukey HSD post-hoc test for specific comparison of Aß1–42+apo E4 and Aß1–42+apo E3 versus Aß1–42 alone, respectively). Chaperoning effect of apo E4 and apo E3 on Aß1–42 fibril formation was significantly reduced if apo E was preincubated with equimolar concentrations of Aß12–28P (dashed red and blue lines; P < 0.01 and P < 0.05 Tukey HSD post-hoc test for specific effect of Aß12–28P on Apo E4 and apo E3, respectively). There were no significant differences between fibrillization curves of Aß1–42 incubated with apo E4 and Aß12–28P or apo E3 and Aß12–28P versus Aß1–42 incubated alone. Aß12–28P alone had no significant effect on Aß1–42 fibril formation.

 
Cell Culture Neurotoxicity Studies

The effect of 1 to 100 µmol/L concentrations of Aß12–28 and Aß12–28P on the viability of the SK-N-SH human neuroblastoma cell line (American Type Culture Collection, Manassas, VA) was compared to the well established neurotoxicity of Aß1–40 and Aß1–42 in this cell line model.24,36,37 Viability of SK-N-SH cells cultured in a flat-bottom, 96-well microtiter plates in the presence of peptides for 2 days, was assessed using the (3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl tetrasodium (MTT) metabolic assay20 according to the manufacturer’s manual (Roche Molecular Biochemicals, Indianapolis, IN).

In toxicity rescue experiments Aß12–28 or Aß12–28P were used to neutralize lipidated apoE4’s effect on Aß1–42 neurotoxicity. Aß12–28 or Aß12–28P was preincubated with apo E4 in an equimolar concentration for 6 hours at 37°C then mixed with Aß1–42, followed by addition to microtiter plates containing SK-N-SH cells. For comparison, cells were incubated with Aß1–42 alone and with Aß1–42 and apoE4. Apo E alone, Aß1–42+Aß12–28 and Aß1–42+Aß12–28P were used as additional controls. The final concentration of peptides was as follows: Aß1–42 100 µmol/L, Aß12–28 and Aß12–28P 0.5 µmol/L and apoE4 0.5 µmol/L. Two- and 6-day experiments were performed and the cell viability was assessed using the MTT assay. All experiments were run in triplicate. The results from cell culture neurotoxicity studies were evaluated by one-way analysis of variance, followed by a Dunnett’s test as a post-hoc analysis.

Competitive Inhibition Assay

Inhibition of Aß1–40 binding to lipidated apoE4 in the presence of Aß12–28P was analyzed by enzyme-linked immunosorbent assay (ELISA).38 ApoE4 100 nmol/L was preincubated with an increasing concentration of Aß12–28P (0 to 400 nmol/L) in 10 mmol/L Tris buffer pH 7.4 for 3 hours at 37°C and then added to immobilized on polystyrene microtiter plates (Immulon-2; Dynatech Lab., Chantilly, VA) Aß1–40 (10 ng/well).38 After another 3 hours of incubation, at the same temperature, the plate was washed and apoE4 bound to Aß1–42 was detected using 3D12 monoclonal antibody (mAb) 1:1000 (Biodesign Int., Saco, MA) followed by incubation with anti-mouse IgG HRP-conjugate (Amersham, Piscataway, NJ) at 1:5000. The color reaction was developed with a 3,3,5,5-tetramethybenzidine substrate (BioRad), and optical density (OD) was measured on a 7520 Microplate Reader (Cambridge Technology, Watertown, MA). Non-specific binding was determined using bovine serum albumin and/or omitting the apoE4 in the assay. OD values were converted to percentages with the binding of apoE4 in the absence of inhibitor being considered as 100%. The mean ± SD (SD) from three independent duplicate experiments was plotted in Figure 3 and analyzed by a one-site competition non-linear regression fit algorithm using GraphPad Prism version 4.0 (GraphPad Software, San Diego, CA).



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  		Figure 3. In a competitive inhibition assay, Aß12–28P (0 to 400 nmol/L/L) was preincubated with 100 nmol/L apoE4 and added to Aß1–40 coated wells. Results are expressed as a percentage of residual apo E4 binding, considering binding of apoE4 in the absence of inhibitor as 100%. Data representing the mean ± SD of three independent duplicate experiments were fitted into one-site competition curve. Half of maximal inhibition (IC50) was calculated to be 36.7 nmol/L.

 
Blood-Brain Permeability Studies

Aß12–28P was labeled with Na[125I] (Amersham) using a two-step reaction. First, sulfo-succinimidyl-4-hydroxybenzoate was coupled (Sulfo-SHB, Pierce, Rockford, Il) to side chain amino groups of lysine residues (Aß positions 16 and 28)39,40 and then these sites were labeled with Na[125I] using IODO-BEADS (Pierce) according to the manufacturer’s instructions. Unbound 125I was removed using a gel filtration column (Bio-Gel P-6, Bio-Rad, Hercules, CA).41 Aß1–40, used for comparison, was tagged with Na[125I] using IODO-BEADS directly.

The blood-brain permeability of Aß12–28P was assessed using the perfusion and capillary depletion techniques42,43 in 10 C57BLJ wild-type mice (22 to 25 g body weight). Animals were anesthetized by intraperitoneal injection of ketamine HCl (0.12 mg/g) and xylazine (0.016 mg/g)44 and their neck vessels were dissected as described elsewhere.42,43 125I-Aß12–28P (12.3 nmol) or 125I -Aß1–40 (11.6 nmol) and inulin [C14]-carboxylic acid (1.33 µCi/mg) as a cerebrovascular space marker (molecular weight = 5175 Da)45 were injected into the right carotid artery and blood samples were collected from the jugular vein on the ipsilateral side. After the infusion was completed, the brain vasculature was washed out with 20 ml of medium without radiolabeled tracers and the animals were sacrificed by decapitation. The brain was instantly removed from the skull, arachnoid membranes were peeled away, and the choroid plexuses were separated by dissection. The ipsilateral hemisphere was homogenized in phosphate-buffered saline (PBS) (1:10 w/v) with a cocktail of protease inhibitors (Complete, Boehringer Mannheim, Mannheim, Germany) and separated from remaining microvasculature by filtrating the homogenate through mesh nylon net with 60-µm pores.46 The 125I and 14C radioactivity in the brain and vessel fractions were determined in a Beckman 4000 gamma counter and a Beckman LS-7000 liquid scintillation spectrometer, respectively (Beckman-Coulter, Fullerton, CA).

Brain uptake of radiolabeled Aß12–28P and Aß1–40 was expressed as perfusion ratio47 VD = CBR/CPL, where CBR and CPL are cpm/g of brain and cpm/µl of serum, respectively. The volume of distribution for a given peptide was corrected for capillary uptake by subtracting VD of inulin from VD of peptide. VD of inulin was on average 14 ± 5 µl/g.

Determination of the Half-Life of Aß12–28P

The half-life of Aß12–28P was determined after a single bolus injection of 80 µg end-protected 125I-Aß12–28P into the femoral vein of six anesthetized wild-type C57BL6J mice. Blood samples were collected at several time points and the concentration of radiolabeled peptide in the serum was assessed using the trichloroacetic (TCA) acid precipitation method, as described elsewhere.45 Bioavailability of 125I-Aß12–28P following intravenous administration was compared with bioavailability following single intranasal administration of the same dose of peptide (80 µg). This experiment was performed in another six wild-type C57BL6J mice which received a diluted peptide in 10-µl drops instilled into both nostrils over 5 minutes.

Radioactivity measurements at separated time points were transformed into percentage values compared to serum radioactivity following intravenous injections at t = 0 as 100%. The mean ± SD from all tested animals was plotted in Figure 4 and analyzed by a one-phase exponential decay non-linear regression fit algorithm using GraphPad Prism version 4.0. To compare the extent of drug bioavailability after the administration of a single intravenous or intranasal dose the area under both curves were calculated.48



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  		Figure 4. Serum level of 125I-Aß12–28P following single intravenous (diamonds) or intranasal (open circles) dose. Values represent percentage of drug serum level considering drug serum level at t = 0 after intravenous administration as 100%. Values are expressed as mean ± SD for all animals studied (n = 6 for intravenous and n = 5 for intranasal). The half-life of Aß12–28P following single intravenous injection was analyzed using one-phase exponential decay non-linear regression fit algorithm. It was calculated to be 62.2 ± 18 minutes.

 
Testing Activity of Aß12–28P in Vivo

Initial testing of Aß12–28P toxicity in vivo was performed on five wild-type C57BL6J mice which received intraperitoneal (i.p.) injections of 1 mg of Aß12–28P diluted in 0.5 ml of sterile PBS three times per week for 4 weeks. Mice were observed for an additional 2 weeks and all remained alive and well. They were monitored for change in body weight, physical appearance, measurable clinical signs, unprovoked behavior, and response to external stimuli.49,50 Following sacrifice, sections from the brain, liver, gut, spleen, kidney, and heart were examined using hematoxylin and eosin staining.

The effect of Aß12–28P on Aß deposition was tested in APPK670N/M671L/PS1M146Ldouble Tg mice.51-53 There were six Aß12–28P-treated and six vehicle-treated sex-matched APPK670N/M671L/PS1M146L mice in this study. The first administration of Aß12–28P or vehicle was begun at 4 months of age, at which time the APPK670N/M671L/PS1M146L mice already have modest numbers of Aß lesions.54,55 The treatment was continued for 4 weeks (1 mg i.p. three times per week) and animals were sacrificed a week after the last injection with an overdose of sodium pentobarbital (150 mg/kg i.p.) and transcardially perfused with PBS and paraformaldehyde as described before.24,56 The brain was cut into serial, 40-µm thick coronal sections using a freezing microtome (Leica SM2400, Nussloch, Germany). Sections were collected in 10 separated series. Each of them contained a complete set of sections spaced 400-µm apart along the rosto-caudal axis of the brain. Cut sections were stored in cryoprotectant (30% sucrose/30% ethylene glycol in 0.1 mol/L phosphate buffer) at –30°C until stained. Aß deposits were stained either with 6E10 mAb (raised against residues 1–16 of Aß57 ) or Thioflavin-S for fibrillar amyloid.58 Details of used immunohistochemical techniques were published previously.24,56,58 Sections stained with 6E10 mAb were developed using 3,3-diaminobenzidine tetrahydrochloride with nickel ammonium sulfate and were not counterstained. This produced black staining of Aß deposits against a transparent background that facilitated selecting density threshold and quantification of Aß deposits. All brains were stained at one time to avoid variability in the intensity of staining that may occur between different batches.

Aß deposits were quantified in the neocortex and in the hippocampus using a random, unbiased sampling scheme and semi-automated image analysis system. First, one of the collected series of brain sections were selected for immunostaining with 6E10 mAb using a random number generator. There are on the average 14 to 15 cross-sections throughout the neocortex and seven cross-sections throughout the hippocampus in each series. This gives a similar number of entries for both structures. In the second step the whole profile of the neocortex and the hippocampus as appearing on the coronal plane cross-sections were traced using the Bioquant image analysis system (R&M Biometrics Inc., Nashville, TN), which randomly superimposed a grid (800 µm x 800 µm) over the traced contour. Test areas (640 µm x 480 µm) were applied by the image analysis system over knots of the grid. With such designed sampling schemes, Aß load was analyzed in 98 ± 16 (mean ± SD) test areas in the neocortex per brain and 31 ± 6 test areas in the hippocampus. About 48% of cross-section area of a structure of interest was covered by a sum of test areas. Efficiency of sampling scheme was verified using an algorithm proposed by West and Gundersen,59-61 whereby the square of variation coefficient for an experimental group should be more than two times larger than the square of error coefficient calculated for Aß load in both the neocortex or the hippocampus in an individual animal in this group. If this condition is met, adding more test areas does not enhance the accuracy of stereological measurements.59 Such a sampling scheme designed in a fully random and unbiased manner helps to counterbalance the natural tendency of Aß to be deposited in a non-homogenous manner in AD Tg mice.

Images of the test areas were captured and a threshold optical density for immunostained Aß plaques was obtained. The black color of Aß deposits and the lack of counterstaining allowed for easy and reliable discrimination of stained objects from the background. Plaques were automatically outlined by the particle analysis protocol of the software, numbered and measured. Objects smaller than 170 µm2 (average cross-sectional area of a hippocampal pyramidal neuron + 2 standard deviations)62,63 were filtered out. The sum of all areas of plaques outlined in a test field and their number in a test field was measured. If needed, artifacts such as non-specific meningeal or vascular staining were eliminated manually. Two parameters Aß load (ie, percentage of test area occupied by Aß) and numerical density of Aß plaques (number of plaques in a test area divided by its area – 0.307 mm2) were calculated. Differences between groups were analyzed by means of the Mann-Whitney U-test.

To demonstrate that the observed treatment effect is not associated with an immune response, plasma of animals treated with Aß12–28P were tested for the presence of antibodies against Aß using a sandwich ELISA.24,64 Plasma of animals vaccinated with Aß homologues peptide, K6Aß1–30, given with Freund’s as an adjuvant, which is known to induce an immune response against Aß, were used as a positive control.24 Mouse sera in increasing range of dilution 1:50 to 1:25600 were applied to Immunolon-2, 96-well microtiter plates coated with Aß1–42 or Aß1–40 and incubated overnight at 4°C. The plates were then washed in PBS, followed by incubation with goat anti-mouse Ig HRP-conjugate (Amersham). Development of color reaction and OD measurements were performed as described above.


   Results
Top
 Abstract
 Materials and Methods
 Results
Discussion
 References
 
Studies of Aß12–28P in Vitro

The secondary structure of peptides was analyzed because an increased ß-sheet content of Aß peptides is a prerequisite for fibril formation and is associated with toxicity. CD measurements performed immediately after reconstitution of peptides with 5 mmol/L Tris buffer (pH 7.0) showed that the secondary structure of Aß12–28 and Aß12–28P is dominated by {alpha}-helix and random coil, which constitute 41% and 57%, or 39% and 59% of the total protein structure, respectively (Table 1) . The ß-sheet content of both peptides was minimal (2%), in contrast to Aß1–42, which had a CD spectrum at time = 0 consistent with 49% ß-sheet content. The secondary structure of Aß12–28 and Aß12–28P remained stable during the 72 hours of incubation at 37°C, whereas the ß-sheet content of Aß1–42 increased from 49% to 58%. These findings were consistent with analysis of fibrillogenic potentials of the studied peptides using the Thioflavin-T assay. Aß12–28P did not form any fibrils during 10 days of incubation (Figure 1A) . In Aß12–28 a small amount of fibrils could be detected following 24 hours of incubation which continued to increase until day 6 when fluorescence levels reached a plateau. However, compared to Aß1–40 or Aß1–42, the amount of fluorescence emitted by the Aß12–28 solution was significantly lower (P < 0.0001, repeated measures analysis of variance; Aß12–28 versus Aß1–40 and Aß12–28 versus Aß1–42 P < 0.001, Tukey HSD post-hoc test). This indicated that the fibrillogenic potential of Aß12–28 is significantly lower than that of full-length Aß peptides.


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  		Table 1. Circular Dichroism Measurements

 
Apo E3 and apo E4 act as pathological chaperones in Aß fibrillization. 3-5,65 In their presence, the amount of fibrils formed by Aß1–42 over time was significantly increased (Figure 1B) . However, when apo E3 or apo E4 were preincubated with Aß12–28P before addition to the Aß1–42 solution, a significantly lower amount of fluorescence was recorded over time (P < 0.0001, repeated measures analysis of variance; P < 0.01 and P < 0.05 Tukey HSD post-hoc test for specific effect of Aß12–28P on Apo E4 and apo E3, respectively). After a 24-hour incubation, a relative reduction in fluorescence by 25.3% was observed for apo E4 and by 14.5% for apo E3, whereas by day 6 the reductions were 50.9% and 54.1% respectively. There were no significant differences between curves produced by Aß1–42 in the presence of apo E3 and E4 inhibited by Aß12–28P and Aß1–42 alone or Aß1–42 with Aß12–28P. However, within 24 hours of incubation the fluorescence of Aß1–42 with apo E and Aß12–28P were higher than those produced by Aß1–42 alone or Aß1–42 with Aß12–28P. Differences between Aß1–42 incubated in the presence of apo E4 and apo E3 versus Aß1–42 alone or Aß1–42 with Aß12–28P were statistically significant (P < 0.01; and P < 0.05). This indicates that in a presence of Aß12–28P both apo E3 and apo E4 have a reduced ability to promote the fibril formation of Aß1–42. Aß12–28P alone had no significant effect on Aß1–42 fibrillogenesis.

No significant reduction in the viability of SK-N-SH human neuroblastoma cells was observed when cells were incubated with Aß12–28 or Aß12–28P at a concentration ranging from 1 µmol/L to 100 µmol/L (Figure 2A) . In contrast, a significantly reduced viability of SK-N-SH cells was noted after a 2-day incubation with Aß1–40 or Aß1–42 starting from concentration as low as 1 µmol/L (P < 0.05 for Aß1–40 and P < 0.01 for Aß 1–42).



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  		Figure 2. Cytotoxicity assay using SK-N-SH human neuroblastoma cells. A: No significant reduction in viability was observed when cells were incubated with Aß12–28 or Aß12–28P. In contrast, even the lowest concentration of Aß1–40 or Aß1–42 resulted in significant cytotoxic effect (one-way analysis of variance P < 0.0001, post-hoc Dunnett’s test P < 0.01 for Aß1–42 and P < 0.05 for Aß1–40 versus control) VEH-vehicle. B: Toxicity of Aß1–42 in cell culture was potentiated in the presence of apo E4 (P < 0.01 Aß1–42 versus Aß1–42/apo E4). This chaperoning effect of apo E could be neutralized if apo E4 was preincubated with Aß12–28 or Aß12–28P (Aß1–42/apo E4 versus Aß1–42/apo E4/Aß12–28 or Aß1–42/apo E4/Aß12–28P P < 0.05 for 2-day assay and P < 0.01 for 6-day assay). Apo E alone did not reduce cell viability. Slightly increased cell viability was observed if Aß1–42 was incubated with Aß12–28P without apo E for 6 days (P < 0.05), but not for 2 days. Adding Aß12–28 to Aß1–42 did not alter cell viability. For clarity of the figure, only significance between Aß1–42/apo E4 versus Aß1–42/apo E4/Aß12–28 and Aß1–42/apo E4/Aß12–28P were marked.

 
In a separate experiment, Aß1–42 (100 µmol/L) was incubated with apo E4 (0.5µmol/L). This produced a significantly greater reduction in cell viability compared to incubation with Aß1–42 alone (P < 0.01 [Figure 2B ]). If the apo E4 was preincubated with an equimolar concentration of either Aß12–28 or Aß12–28P before adding to Aß1–42 a significant rescue of the cell viability could be demonstrated (P < 0.05 for the 2-day time point and P < 0.01 for the 6-day time point). The viability of SK-N-SH cells incubated in the presence of apo E4 alone (0.5 µmol/L) was not significantly reduced compared to the control group (only vehicle added). Slightly increased cell viability was observed if Aß1–42 (100 µmol/L) was incubated with Aß12–28P (0.5 µmol/L) without apo E for 6 days (P < 0.05), but not for 2 days.

Pharmacokinetic and Blood-Brain Barrier Permeability Studies

A competitive inhibition assay was performed to demonstrate the ability of Aß12–28P to specifically bind to apoE and block the binding to the full-length Aß peptide. Preincubation of apoE4 with increasing concentrations of Aß12–28P resulted in decreased affinity toward immobilized Aß1–40 (Figure 3) . The concentration of Aß12–28P producing half-maximal inhibition (IC50) was calculated from a non-linear regression, one-site competition curve as 36.7 nmol/L. The inhibition constant (KI) of Aß12–28P was calculated to be 11.37 nmol, given the known dissociation constant (KD) of Aß1–40 binding to apoE is approximately 10 nmol.14,66

Aß12–28P was synthesized from D-amino acids and end-protected to prevent its biodegradation and extend its potential therapeutic effect. The plasma half-life of Aß12–28P was estimated from intravenous injection of a single dose of 125I-Aß12–28P experiment to be 62.2 ± 18 minutes (mean ± SD) (Figure 4) . This contrasts with a plasma half life of 2 to 3 minutes for non-end-protected Aß1–40.67 The presence of 125I- Aß12–28P in the serum could also be demonstrated following intranasal administration. At t = 0 the serum level was equal to about 40% of the level achieved after administration of the same amount of peptide intravenously. In contrast to the serum profile, where the level of peptide decreased sharply, following intranasal administration, the serum level remained stable for the first hour and then started to decrease slowly, matching the level of peptide after intravenous administration at t = 3 hours. However, when the areas under the curve for intravenous and intranasal administration were calculated, no significant differences were found. This indicates that the extent of drug bioavailability after intravenous administration is comparable to bioavailability of the same dose administered intranasally.

An inhibitor of apoE/Aß binding has to be able to cross the BBB to exert its therapeutic effect. The BBB permeability of Aß12–28P was studied using the brain perfusion and capillary depletion techniques. The volume of distribution (VD) of 125I- Aß12–28P after trans-carotid perfusion was calculated to be 65 ± 20 µl/gram of brain tissue (mean ± SD) whereas the VD of 125I- Aß1–40 under the same experimental conditions was 81.3 ± 40 µl/gram (difference not statistically significant). More than 90% of 125I- Aß12–28P was found in the capillary-depleted brain fraction indicating that the majority of the peptide crossed into the brain parenchyma and was not retained in the vascular compartment.

Reduction of Aß-Load in APP/PS1 Mice after Aß12–28P Treatment

Before testing the effect of Aß12–28P on Aß load in Tg mice, a toxicity test was carried out using five wild-type mice which received 1 mg of Aß12–28P three times a week for 4 weeks; the same protocol later used on the Tg mice. No changes were noted in treated animals in terms of body weight, physical appearance, unprovoked behavior or response to external stimuli. Hematoxylin and eosin-stained sections of the brain, heart, liver, gut, spleen, or kidneys did not reveal any pathology.

Treatment with Aß12–28P was started at the age of 4 months. After 4 weeks of peptide administration, the Aß load in the neocortex and in the hippocampus of treated animals was 63.3% (P = 0.0043) and 59.5% (P = 0.0087) lower compared to age-matched control Tg animals, which received vehicle (Figure 5A and Figure 6, A and B ). There was also a reduction in the numerical density of Aß plaques in treated mice by 60.1% in the neocortex (P = 0.0079) and by 49.6% in the hippocampus (P = 0.0043) (Figure 5B) . The reduction in the density of Aß plaques was also seen on Thioflavin-S staining which selectively labels Aß deposits in a fibrillar form (Figure 7) .



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  		Figure 5. Significant reduction in the area covered by Aß (Aß load [A]) and in numerical density of Aß plaques [B] was observed in APP K670N/M671L/PS1M146L Tg mice treated with Aß12–28P compared to age-matched Tg control animals treated with placebo.

 


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  		Figure 6. Hemispheric sections of APPK670N/M671L/PS1M146L Tg mice treated with Aß12–28P (A) and with vehicle (B). Reduced density of Aß deposits following 4 weeks of treatment with Aß12–28P is evident compared to age-matched control double Tg. 6E10 mAb immunohistochemistry; bar, 500µm.

 


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  		Figure 7. Reduction in numerical density and cross-section area of plaques were also noticed on sections stained with Thioflavin-S for fibrillar Aß. A and C, treated animals; B and D, vehicle. A and B, neocortex; bar, 500 µm. C and D, hippocampus; bar, 125 µm.

 
Treatment with Aß12–28P had a marked effect on reducing the density of plaques in all size categories. There was a 52.8% reduction in the density of small plaques (cross-section area < 500 µm2, P < 0.0043), a 53.5% reduction in the number of medium-size plaques (cross-section area > 500 µm2 and < 1000 µm2; P < 0.05), and a 44% reduction in the number of large plaques (> 1000 µm2; non-significant) in the neocortex (Figure 8A) . In the hippocampus, the reduction in the density of plaques in each size category was 37.6% for small plaques (P < 0.05), 48.6% for medium-size plaques (P < 0.05), and 65.4% for large plaques (P < 0.05, Figure 8B ).



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  		Figure 8. Treatment with Aß12–28P resulted in reduced number of small (< 500 µm2), medium-sized (> 500-< 1000 µm2), and large plaques (> 1000 µm2) both in the cortex (A) and in the hippocampus (B). This demonstrates an effect of inhibition of pathological chaperones on the development of new Aß plaques. *, P < 0.05; **, P < 0.01, Mann-Whitney U-test.

 
At the time of sacrifice, sera of wild-type and Tg mice treated with Aß12–28P were collected and tested for presence of anti-Aß antibodies. No anti-Aß antibodies were detected in mice treated with Aß12–28P, whereas under the same conditions, positive control, sera of APP K670N/M671L mice immunized with K6Aß1–30-NH2 and Freund’s adjuvant,24 showed the presence of anti-Aß antibodies with a titer ranging from 1:1000 to 1:10,000. This indicates that the effect of Aß12–28P on Aß load cannot be attributed to a humoral response against Aß.


   Discussion
Top
 Abstract
 Materials and Methods
 Results
 Discussion
References
 
Accumulation of Aß, a 39–43 amino acid peptide, in brains of AD patients is a hallmark of AD pathology.68 Complementary pieces of evidences derived from in vivo and in vitro studies have demonstrated that apoE critically promotes Aß fibrillization and deposition.20 The most striking example, emphasizing the role of apoE as a pathological chaperone of ß -amyloidosis comes from experiments with generation of APPV717F/apoE–/– mice which have a delayed onset of Aß deposition, a reduced Aß load, and no fibrillar Aß deposits, compared to APPV717F/apoE+/+ Tg mice. APPV717F/apoE+/- mice demonstrate an intermediate level of pathology.12,69-71 Neutralization of the chaperoning effect of apoE would therefore have a mitigating effect on Aß accumulation. To investigate this potentially therapeutic mechanism, we synthesized a peptide homologous to residues 12–28 of Aß which is a specific apoE binding domain.13,18 Such peptide could attach to apoE preventing its binding to the full-length Aß.20 To avoid intrinsic toxicity associated with its residual capacity to form fibrils and hence ability to co-deposit on existing plaques, the sequence of Aß12–28 was modified by replacing valine for proline in position 18. This rendered Aß12–28P non-fibrillogenic, as demonstrated by CD and Thioflavin-T aggregation assays, as well as non-toxic in cell culture. These modifications did not modify the affinity of Aß12–28P to apoE. In a competitive inhibition assay, Aß12–28P reacted with lipidated apoE preventing its binding to full-length Aß with IC50 = 36.7 nmol/L. An effect of apoE on Aß fibril formation and toxicity in cell culture was significantly reduced in the presence of Aß12–28P. Synthesis of Aß12–28P with end-protection and using of D-amino acids extended its half-life in the serum to 62 minutes, contrasting with the very short half-life of L-amino acid, non-end-protected Aß1–40 (2 to 3 minutes).67 Aß12–28P is BBB permeable allowing for an in vivo effect within the brain. APPK670N/M671L/PS1M146L AD Tg mice treated with Aß12–28P had a significantly lower Aß load, similar to what is observed in mice with decreased apoE expression.12,69-71 The initial Aß plaques in APPK670N/M671L/PS1M146L mice appear at 3 months of age; whereas, between the fourth and the fifth months of life, Aß deposition follows an exponential curve where new plaques are actively formed.54 We show that administration of Aß12–28P for a period as short as 1 month resulted in an over twofold reduction in Aß load and plaque density compared to untreated age-matched Tg animals. An effect of Aß12–28P on Aß deposition occurs without a humoral response since we did not detect any anti-Aß antibodies in the sera of treated animals.

Little is known about dynamic plaque growth in vivo. Early, in vitro models have suggested that Aß deposits may grow by deposition of soluble Aß72 and that apo E is critical for this process (for review, see Tomiyama et al3 ). More recently, Christie et al73 using in vivo multiphoton microscopy demonstrated that the size of already formed Aß deposits remains unchanged in 18-month-old Tg2776 AD Tg mice over 5 months of longitudinal observations. In addition, an average diameter of a plaque stained with Thioflavin-S in Tg mouse brain does not change appreciably between 12 and 22 months, although plaque density increases between these time points almost sixfold.73 In our study, treated mice showed a decreased density of plaques in all size categories implying that blocking the Aß/apo E interaction in vivo decreases the rate of new plaque formation. Whether or not this form of treatment may also have an effect on the growth dynamic of plaques remains to be confirmed.

Although in vitro Aß homologous peptides can aggregate and form fibrils spontaneously, with apo E acting only to accelerate this process,4,5 it is likely that in vivo Aß oligomerization and deposition is much more dependent on the presence of apo E.74 In vitro fibrillization experiments demonstrated that proportionally minute amount of apoE can exert a chaperoning effect with molar Aß:apoE ratio being 100 to 200:1.4,5 This shows that a very small amount of apoE is sufficient to propagate fibril formation and indicates that only a small amount of apoE has to be pharmacologically targeted. Therefore even with limited BBB permeability, a therapeutic effect of Aß12–28P could be demonstrated in vivo.

The pharmacological targeting of apoE has to take into account that apoE is involved in the clearance of Aß from the central nervous system (CNS) across the BBB in addition to a role as a pathological chaperone.75,76 ApoE KO mice and mice expressing human apoE4 on murine apoE KO background have impaired clearance of synthetic Aß injected into the brain parenchyma compared to mice expressing human isoform apoE3.77 Therefore, apoE plays a dual role in Aß clearance and deposition, which is likely dependent on the concentration of CNS Aß and that of other Aß binding proteins. Given the opposing roles apoE has on Aß peptides in the CNS, it is conceivable that blocking apoE/Aß binding would increase the amyloid burden. However, it appears that the role of apo E as a pathological chaperone outweighs its role in Aß clearance since APPV717F/apoE –/– mice have a decrease in both Aß load and level.12,69-71 Similarly, our pharmacological blocking of the Aß/apoE interaction in this study is consistent with the dominance of a pathological chaperone function. Evidence comparing Aß levels in APPV717F Tg mouse strains crossed to either apoE or apoJ KO lines suggest that apoJ and apoE can effectively replace each other in their Aß clearance function. It is only when both apoJ and apoE are knocked out that Aß amyloid deposition is increased.78

AD is a progressive disease for which only palliative treatment is currently available. A number of potential new therapeutic approaches targeting pathological biology of AD, and ß-amyloidosis in particular, are emerging. The vaccination approach has shown great promise in model animals;24,79-81 however, human trials have shown toxicity to be a major problem.82 Targeting the secretase enzymes which are responsible for releasing Aß from APP has also been a major therapeutic focus. However, these enzymes are involved in several other functions83-86 and selective inhibition of Aß cleavage without associated significant toxicity is a substantial issue. Compared to vaccination87 or {gamma}-secretase inhibitors,88 blocking of pathological chaperones is not associated with the risk of an autoimmune reaction or affecting multiple signaling pathways including Notch-1 and wnt.86 Animals treated with Aß12–28P did not produce a humoral response related to the peptide’s small size and because no adjuvant was administered. Our data demonstrates that inhibiting Aß/apoE interaction over a relatively short period of time can have dramatic effects on amyloid burden, highlighting the importance of apoE in the balance of clearance versus aggregation/deposition of Aß. Therefore, inhibitors of Aß pathological chaperones may be an alternative approach for the treatment of AD amyloidosis. Results of this initial study make this concept worthy of further exploration including biochemical and behavioral characterization of treatment effects in various AD Tg models co-expressing familial AD-linked mutations and the different allelic forms of the human apoE gene.


   Footnotes
 
Address reprint requests to Dr. Thomas Wisniewski, New York University School of Medicine, HN419, 550 First Avenue, New York, New York 10016. E-mail: thomas.wisniewski{at}med.nyu.edu

Supported by National Institues of Health grants AG15408 (T.W.), AG20747 (M.S.), and AG13956 (D.M.H.).

This manuscript is dedicated to the memory of Prof. Henry Wisniewski.

Accepted for publication June 1, 2004.


   References
Top
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 Materials and Methods
 Results
 Discussion
 References
 

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