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The cerebral accumulation of β-amyloid (Aβ) is a consistent feature of and likely contributor to the development of Alzheimer’s Disease (AD). In addition to dysregulated production, increasing experimental evidence suggests reduced catabolism also plays an important role in Aβ accumulation. We have previously shown that neprilysin (NEP), the major protease which cleaves Aβ in vivo, is modified by 4-hydroxy-nonenal (HNE) adducts in the brain of AD patients. In order to determine if these changes affected Aβ, SH-SY5Y cells were treated with HNE or Aβ, and then NEP mRNA, protein levels, HNE adducted NEP, NEP activity and secreted Aβ levels were determined. Intracellular NEP developed HNE adducts after 24 h of HNE treatment as determined by immunoprecipitation, immunoblotting and double immunofluorescence staining. HNE-modified NEP showed decreased catalytic activity, which was associated with elevations in Aβ1-40 in SH-SY5Y and H4 APP695wt cells. Incubation of cells with Aβ1-42 also induced HNE adduction of NEP. In an apparent compensatory response, Aβ treated cells showed increased NEP mRNA and protein expression. Despite elevations in NEP protein, the activity was significantly lower compared to the NEP protein level. The present study demonstrates that NEP can be inactivated by HNE-adduction, which is associated with, at least partly, reduced Aβ cleavage and enhanced Aβ accumulation.
Alzheimer’s disease (AD) is a progressive neurodegenerative disorder that gradually damages the neocortex and hippocampus, reducing memory, learning and reasoning (Selkoe 2001). AD is characterized by extensive amyloid deposition, neurofibrillary tangles (NFT), inflammation, and ultimately synaptic and neuronal loss (Wang et al. 2006, 2008). A large body of evidence suggests that the accumulation of β-amyloid (Aβ) is a crucial event in the initiation and maintenance of neuronal degeneration in AD (Bard et al. 2000; Selkoe 2001; Hardy and Selkoe 2002; Forman et al. 2004). Aβ neurotoxicity has been demonstrated both in vitro (Yankner et al. 1990; Pike et al. 1995) and in vivo (Kowall et al. 1992; Frautschy et al. 1996; Hardy 1997). Although the mechanisms that contribute to abnormal Aβ accumulation are not fully understood, both increased production and decreased degradation have been observed. Despite its importance Aβ catabolism remains understudied (Saido and Iwata 2006).
In normal brain, rapid proteolysis attenuates Aβ accumulation. The degradation process occurs primarily through the action of a group of peptidases including neprilysin (NEP), insulysin (insulin degrading enzyme, IDE) and endothelin converting enzyme (ECE). NEP appears to be the predominant Aβ protease (Carson and Turner 2002; Eckman and Eckman 2005; Vardy et al. 2005; Wang et al. 2006). NEP (also known as neutral endopeptidase, EC220.127.116.11, enkephalinase, and CD10) is a 97 kDa type II membrane-bound zinc metalloendopeptidase. NEP is ubiquitously expressed by neurons, and is capable of degrading both monomeric and oligomeric forms of Aβ and several other neuropeptides (Higuchi et al. 2005). NEP expression is reduced in the hippocampus and cortex of aged mice (Iwata et al. 2002; Apelt et al. 2003; Caccamo et al. 2005) while Aβ is elevated in NEP KO mice or those treated with NEP inhibitors (Iwata et al. 2001; Marr et al. 2004; Turner et al. 2004). Conversely, over-expression of NEP reduced Aβ levels in a dose-dependent manner (Iwata et al. 2004; Marr et al. 2004) and protected neurons from Aβ toxicity in vitro (El-Amouri et al. 2007).
In addition to age-dependent changes, neurons in the vicinity of abundant plaques showed reduced NEP mRNA and protein levels when compared to age-matched normal controls (Yasojima et al. 2001b; Yasojima et al. 2001a; Wang et al. 2003; Caccamo et al. 2005; Wang et al. 2005). We showed that NEP was selectively decreased in AD brains but not in pathological aging (PA) (Wang et al. 2005). The greatest reductions occurred in regions most vulnerable to AD pathology, such as hippocampus and association cortex while the cerebellum or peripheral organs were spared (Yasojima et al. 2001b; Caccamo et al. 2005). NEP levels were inversely correlated with senile plaque counts and total Aβ levels in cortical homogenates and positively correlated with clinical cognitive scores (Wang et al. 2005). These data support the hypothesis that decreased NEP contributes to Aβ deposition and neuronal dysfunction in AD.
Oxidative stress has long been recognized as a contributing, early factor in AD (Smith et al. 1991; Harman 1993; Olanow 1993; Smith et al. 1995; Smith et al. 2000; Varadarajan et al. 2000). Aβ induces free radical generation (Smith et al. 1991; Montine et al. 1996; Sayre et al. 1997; Pratico et al. 1998; Nunomura et al. 2001; Nunomura et al. 2004; David et al. 2005; Schuessel et al. 2005; Shi and Gibson 2007) and elevated 4-hydroxynonenal (4-HNE), a marker of lipid peroxidation, is present in plaques (Ando et al. 1998). HNE can interact with and inactivate a variety of enzymes including NEP (Wang et al. 2003). Here, we show that NEP can be modified in vitro by exogenous HNE or by HNE induced by Aβ from cultured human neuroblastoma cell lines. HNE-adduction reduced NEP activity and attenuated Aβ turnover. Stressed neuroblastoma cells showed compensatory increases in NEP expression but lower total activity. Therefore, the effects of oxidative stress on NEP and Aβ accumulation can be modeled in vitro.
Synthetic human β-amyloid peptide 1-42 were purchased from BACHEM. Dithiothreitol (DTT), protease inhibitors cocktail (P8430) were obtained from Sigma-Aldrich. 4-Hydroxy-2-nonenal (HNE) was obtained from A.G. Scientific, Inc. Mac-R-P-P-G-F-S-A-F-K (Dnp)-OH Fluorogenic Peptide Substrate V, RNAse-free DNase came from R&D and Promega, respectively. GE nitrocellulose membrane was purchased from ISC BioExpress. An enhanced emiLuminescence (ECL) kit and Seize® Classic (G) Immunoprecipitation Kit were obtained from Pierce. Human neprilysin ELISA kit and Aβ1-40 protein ELISA kit are from R&D and Invitrogen, respectively. Other general chemicals and reagents were from Fisher Scientific.
Antibodies were from the following sources: Rabbit anti-HNE and Rabbit anti-NEP antibody (Chemicon); CD10 clonal 56C6 (Thermo Scientific). Anti-human/mouse Rhodamine conjugated affinity purified secondary antibody, goat anti-rabbit fluorescein conjugated secondary antibody, HRP conjugated secondary antibody were purchased from Chemicon.
SH-SY5Y neuroblastoma cells, obtained from the American Type Culture Collection (ATCC), were maintained in a humidified atmosphere of 95% air and 5% CO2 at 37°C. Cells were seeded into plates or dishes in DMEM/F12 (1:1) medium, supplemented with 10% (v/v) fetal bovine serum (FBS), 100 U/ml penicillin and 100 μg/ml streptomycin.
Human neuroglioma H4 cell line was obtained from ATCC (item number: HTB-148). H4 cells stably transfected with human βAPP695wt cDNA under control of a CMV promoter (pcDNA3, Invitrogen) was kindly provided by B.C Eckman’s lab (Mayo Clinic, Jacksonville). H4 were grown in Opti-MEM (Gibco). The media were supplemented with 10% FBS and penicillin/streptomycin. The polyclonal H4 APP695wt line was maintained in 500 μg/ml geneticin (Gibco).
SH-SY5Y cells were seeded into 100 mm dishes at a density of 2 × 104 cells per ml. Experiments were carried out 24–48 h after cells were seeded. Different concentrations of HNE (dissolved in 3% DMSO) or Aβ (dissolved in 0.4% DMSO) were added to the cultures 24 h before harvest. Final concentrations of DMSO in medium were <0.003%. Vehicles (with same concentrations of DMSO) were added to the cultures as controls.
Total RNA from a well of 6-wells plate was isolated using the RNeasy kit (Qiagen Inc., Valencia, CA) according to the manufacturer’s instructions. The concentration of nucleic acids was determined spectrophotometrically at 260 nm and 280 nm, taking into account the dilution factor. RQ1 RNase-free DNase (Promega) was used to remove relict of DNA which might interfere the output of PCR. For the PCR first strand synthesis was performed using the Omiscript® RT Kit (Qiagen Inc.). The resulting cDNA was then assayed by real time PCR.
Real time PCR was performed in 0.2 ml thin wall PCR plates using the iCycler thermal cycler (Bio-rad) and carried out with iQ SYBR Green supermix (Bio-rad) according to the manufacturer’s instructions. The standard reaction mix consisted of iQ SYBR Green supermix, forward and reverse primers at a final concentration of 500 nM each, 10 pg DNA template, DNase free water to give final volume of 20 μl. The mixture was heated to 95°C for 3 min followed by 35 cycles with denaturation at 95°C for 30 s, annealing at 60°C for 30 s and extension at 72°C for 30 s. Human S26 was used as reference gene. Primer sequences for real time PCR: S26:5′-CGC AGC AGT CAG GGA CAT TT-3′ (F), 5′-TTC ACA TAC AGC TTG GGA AGC-3′ (R); NEP: 5′-GCC TCA GCC GAA CCT ACA AG-3′ (F), 5′-AGT TTG CAC AAC GTC CTC AAG TT-3′ (R).
Relative quantification of genes expression was carried out by comparative Ct method according to manufacture’s protocol (User Bulletin #2: ABI PRISM 7700 Sequence Detection System). Briefly, the genes mRNA level was expressed in cycle threshold (Ct) value; the Ct values for each sample were averaged from duplicate. Differences between the mean Ct values of NEP and reference gene were calculated as ΔCtsample= Ct NEP−Ct s26 for different treated groups, and that of the ΔCt for the control groups were set for calibrator (ΔCtcalibrator). Final results, the sample-calibrator ratio, expressed as N-fold differences of NEP expression in the HNE or Aβ1-42 groups compared with control, were determined as 2−(ΔCt sample−ΔCt calibrator).
After incubation with HNE (5 and 10 μM) or Aβ (1 and 2 μM) for 24 h, cells were harvested, lysed in Passive Lysis Buffer containing protease inhibitors cocktail (Sigma P8430). Lysates were incubated for 30 min on ice, and then centrifuged at 10,000 × g for 10 min at 4 °C. Protein concentration in the supernatant was determined by Coomassie blue protein binding method using protein quantification Kit-rapid (Sigma/Fluka) with bovine serum albumin as standard. The same amount of protein from HNE-treated, Aβ1-42 and vehicle-treated cells were used for western blotting assay and immunoprecipitation.
For NEP protein levels detection, samples containing equal amounts of protein were denatured in protein sample buffer (100 mM Tris-Cl pH 6.8, 4% SDS, 0.2% bromophenol blue, 20% glycerol, 20% H2O, 200 mM DTT) at 100°C for 10 min and loaded, separated on 10% SDS–polyacrylamide gels and transferred to nitrocellulose membranes in a Bio-rad electrophoresis system. After blocking with TBST containing 5% non-fat milk, the membranes were kept at 4 °C overnight with primary antibodies (1:5000 for β-actin, 1:1000 for NEP, respectively), followed by HRP-conjugated secondary antibodies (1:5000 to 1:10000 dilution) at room temperature for 2 h. The target protein bands were detected using the ECL Western blotting detection system (Pierce) and autoradiography film (Fisher).
Immunoprecipitation with anti-NEP was performed with Seize® Classic (G) Immunoprecipitation Kit according to the manufacturer’s protocol. For total cell extract preparation, SH-SY5Y cells were lysed in Passive Lysis Buffer containing protease inhibitors cocktail (P8430, Sigma). Lysates were incubated for 30 min on ice, and then centrifuged at 10,000 × g for 15 min at 4°C. Supernatants with same amount of protein were incubated with rabbit anti-NEP polyclonal antibody (Chemicon, 1 μg/ml) at 4°C overnight. After washing Immobilized Protein G by adding 0.4 ml of BupH™ Modified Dulbecco’s PBS twice, the immune complexes were added to the spin cup containing the equilibrated immobilized protein G and incubated for more than 1 hour at 4°C. The samples were centrifuged briefly to remove the flow-through solution. The beads were extensively washed with BupH™ Modified Dulbecco’s PBS. The immunoprecipitated proteins were eluted by adding equal volume of ImmunoPure® Elution Buffer and then analyzed by Western blotting with anti-HNE and anti-NEP antibodies.
Cells were fixed with 4% paraformaldehyde at room temperature (RT) for 20 min and permeabilized with 0.2% Triton X-100 in PBS. After blocking for 1 h at RT with 1% goat serum/PBS, cells were incubated overnight at 4°C in a humidity chamber with primary anti-NEP (1:200). At the end of the incubation, the cells were rinsed three times with PBS-Tween-20 (0.05%) and incubated with the FITC conjugated goat anti-rat (1:50) for 60 min at room temperature. Then the cells were fixed with 4% paraformaldehyde at RT for 15 min. After rinsing with PBS for 3 times, second primary rabbit anti-HNE (1:200) were added and incubated for 2 h at RT or overnight at 4°C. Secondary, TRITC conjugated anti-rabbit IgG (1:50) were incubated for another 60 min at RT. All primary and secondary antibodies were diluted in PBS with 1% normal goat serum. After a rinse with PBS, the cells were photographed and analyzed with a fluorescent microscope (Nikon, E600, Japan). The immunofluorescence staining was done at least three times to assess the reproducibility of the results. In order to confirm the specificity of immunostaining for the second cycle, the primary or secondary antibodies were omitted or replaced with preimmue IgG.
NEP activity was determined by Fluorescence Resonance Energy Transfer (FRET). After extraction with a final concentration of 0.1% Triton X-100 in phosphate-buffered saline (PBS; pH 7.4) for 30 minutes on ice, NEP activity in cell lysates was analyzed using a synthetic NEP fluorogenic peptide substrate (Mca-RPPGFSAFK[Dnp]-OH; R&D Systems, Inc., Minneapolis, MN) (Johnson and Ahn 2000) at room temperature in the presence or absence of the NEP inhibitor, thiorphan. Samples dissolved in 50 mM HEPES buffer [pH 7.5] were preincubated with 10 μM thiorphan or PBS for 10 minutes prior to adding fluorogenic peptide substrate (dissolved in HEPES). Fluorescence was read after excitation at 320 nm and emission at 405 nm on a fluorescent ELISA plate reader (Spectra Max Gemini; Molecular Devices, Sunnyvale, CA). For kinetic analysis the cell lysates were incubated with increasing concentrations of substrate (4–20 μM) at room temperature. Fluorescence over the time was measured for 1 hour. The specific NEP activity was determined as the fluorescence difference occurring in the presence or absence of 10 μM thiorphan. Kinetic isotherms (Vmax and Km values) for NEP activity were determined by means of non-linear least squares fitting to the Michaelis-Menten equation using GraphPad Prim software (version 3.0 for Windows, ISI Software San Diego. CA, USA).
To measure the activity of membrane-bound enzyme, cell suspensions were prepared, then washed with PBS. 5 × 104 cells were resuspended in 50 μl of PBS contained in each well of black microtiter plates. The 50 μl substrate (10 μM in 50 mM HEPES) was added, and incubated at room temperature for 60 min. As above, thiorphan was used to determine the specific NEP activity in intact cells.
Cells treated by vehicles, HNE or Aβ1-42 were lysated with Passive Lysis Buffer containing protease inhibitors cocktail (Sigma P8430). After 30 min incubation on ice, the lysates were centrifuged at 1300 rpm for 15 min at 4°C. Every single sample was assigned to the assays of NEP level (ELISA) and NEP activity (immunocapture-based).
NEP protein level and specific activity were measured by using DuoSet® ELISA kit (R&D). Sandwich ELISA assay of NEP was performed according to the protocol provided by manufacturer. Standard curves were produced from serial dilutions of recombinant human NEP.
For the immunocapure-based NEP activity (Miners et al, 2008), 96-well high binding ELISA plates (BD) were coated with 100 μl capture NEP (goat anti-human, 1.6 μg/mL) antibody diluted in PBS (137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.5 mM KH2PO4, pH 7.2) and left for 18 h at room temperature. The plates were washed with PBS containing 0.05% tween-20 for 3 times. After 60 min blocking with PBS containing 1% BSA fraction V, 100 μL of standards or supernatants were added and incubated at 4°C overnight. After 3 washes, the fluorogenic peptide (10 μM) diluted in 100 mM Tris-HCl pH 7.5, 50 mM NaCl and 10 μM ZnCl2 was added and incubated at 37°C in dark. Fluorescent readings were taken after 60 min. Control wells included in each plate contained PBS and fluoregenic peptide..
3 ml of SH-SY5Y and H4 APP695wt cells suspensions were seeded into 6-well plates. The cells were then allowed to grow to confluence (resting phase). The medium in each well was replaced with 1 ml of the appropriate fresh media and treated with 5, 10 and 20 μM HNE for 24 h after which the media were collected. Sandwich ELISAs for the detection of Aβ was performed according to the protocol provided by manufacturer (Biosource). In brief, 50 μl of Aβ peptide standards, controls and dilutions of samples were added into wells pre-coated with primary antibody specific for the NH2-terminus of Human Aβ (capture antibody) and allowed to incubate overnight at 4°C. 50 μl/well of secondary (detection) antibody was allowed to bind 4 h at room temperature. After 4 washes with buffer, 100 μl/well anti-rabbit Ig’s-HRP solution was added and continuously incubated for 30 min at room temperature. Developing was performed using stabilized chromogen (TMB) and the reaction stopped by the addition of 100 μl of stop solution. Plates were read at 450 nm in a SpectraMax Plus spectrophotometer (Molecular Devices) and analyzed by SOFTmax® PRO software. Aβ values in the unknowns were calculated by comparison to the values obtained for the synthetic Aβ standards analyzed on the same plate.
All results are given as mean ± SEM. Statistical analyses were performed with One-way ANOVA followed by least significant difference post hoc analysis (multiple comparisons) and t-test with threshold of P < 0.05.
First we evaluated the effects of HNE and Aβ on intracellular NEP mRNA and protein expression. Vehicle, HNE or Aβ treated SH-SY5Y cells were analyzed by real-time PCR analysis for NEP mRNA. Cells exposed to HNE (5 and 10 μM) for 6 hours showed a marked reduction in NEP expression, which rebounded after 12 hours (Figure 1A). Treatment for 6 hours with Aβ had no effect, but significantly up-regulated NEP mRNA expression at 12 hours (Figure 1B). NEP protein levels as determined by western blotting displayed no change after HNE treatments, but significantly increased (P < 0.05) in Aβ1-42-treated cells (Figure 2).
In order to determine if HNE-modification to NEP occurred in the cultured SH-SY5Y cells treated with HNE or Aβ1-42, NEP protein was immunoprecipitated with rabbit polyclonal anti-NEP antibody followed by western blot with an anti-HNE and anti-NEP antibody respectively (Figure 3). The data suggests that NEP was modified by HNE in both HNE- and Aβ-treated cells (Figure 3A). Quantification showed that NEP in HNE-treated cells was similar to the control, but approximately 60% higher in Aβ-treated cell. HNE levels in both HNE- and Aβ-treated cell were about 200% higher than in control. The ratio of HNE to NEP was 180% and 140% higher to control respectively after HNE and Aβ-treated cell (Figure 3B).
In order to determine the subcellular location of modified protein, we performed double fluorescence staining followed by confocal analysis of oxidatively stressed SH-SY5Y cells (Figure 4). HNE was undetectable in controls (Figure 4b) but positive in a punctal pattern both in HNE and Aβ treated cells (Figure 4e, h). Merged images revealed NEP and HNE colocalized in cells treated with HNE or Aβ (Figure 4f, i) consistent with the results observed after western blotting and immunoprecipitation. Therefore, NEP is modified by exogenously added or endogenously produced HNE induced by Aβ (Figure 4). Furthermore, these results suggest that SH-SY5Y cell is a valid system to study these events at a molecular level.
Given the substantial adduction of NEP, we hypothesized its proteolytic activity would be attenuated. Therefore, NEP activity in lysates or intact SH-SY5Y cells treated for 24h was determined with a commercially available fluorogenic substrate. The activity assay was highly sensitive, linear over-time (up to 60 min examined, data not shown) and sensitive to the NEP inhibitor, thiorphan (data not shown). Treatment of cells with HNE led to a concentration dependent loss of total NEP activity, particularly in intact cells (Figure 5A). Specific NEP activity in cell lysates was decreased ~25% (P < 0.05) (data not shown) while intact cells showed up to a 50% reduction (Figure 5B). Despite adduction, samples treated with Aβ showed increased NEP activity (Figure 5C–D).
To further analyze these results, NEP activity was compared over a range of substrate concentrations (4–16μM) in SH-SY5Y cells. Activity was saturable, and followed Michealis-Menten kinetics in all cell lysates treated with vehicle, HNE and Aβ peptide. Lineweaver-Burk double-reciprocal plots of reaction velocities and substrate concentrations allowed calculation of the apparent Michaelis Constant (Km) for the enzyme in all samples (Table 1, KFigure 6). After HNE treatment, the m was significantly increased compared to control which implies that the enzyme affinity for substrate was decreased (Table 1). There was no significant effect on the Km (Table 1) at any of the three concentrations of Aβ. Vmax was unchanged after HNE but tended to increase after Aβ which likely reflects increased concentration of NEP.
The unexpected results from Aβ treatments prompted us to further explore the underlying mechanisms. Using NEP ELISA assay and immuno-captured activity approach, we measured and compared NEP protein level and specific NEP activity in the same samples and compared in pairs. NEP protein did not show obvious changes in HNE treated cells, but obviously increased in Aβ treatments. This conclusion is consistent with the moderate increases in NEP levels seen by immunoblot and immunofluorescence staining.
Consistent with the alteration of activity directly measured in cell lysates and intact cells, HNE at different concentration significantly lowered the NEP activity. In Aβ treated group, NEP activity showed moderate increase when compared to the vehicle control, but there was no statistical significance. However, the activities were all lower than protein levels when compare NEP protein and NEP activity in pairs (Figure 5E and F), which further confirmed the modification of NEP after HNE and Aβ treatments.
The above results predict that oxidative inactivation of NEP would reduce Aβ catabolism. We tested this using SH-SY5Y and human H4 APPwt cells. The latter are stably transfected with human APP695 cDNA driven by a CMV promoter. As shown in Figure 7, HNE treatment over a range of concentrations increased Aβ levels in the supernatant of both cell lines. Similar effects were seen in H4 APPwt cells despite the much higher basal expression of Aβ (11.01 ± 0.33 pg/ml vs 59.18 ± 0.90 pg/ml).
The formation of HNE is initiated by oxidative stress and culminates in membrane lipid, DNA and protein peroxidation. The HNE–macromolecular adducts are abundant in the brain of patients with AD consistent with a role for oxidative damage in disease pathogenesis (Sayre et al. 1997; Ando et al. 1998; Takeda et al. 2000). NEP is clearly one of the targets of HNE mediated modification in AD brain which likely contributed to accelerated NEP catabolism and reduced levels compared to controls (Wang et al. 2003). The data also suggested that dysregulated NEP function may compromise Aβ degradation. However, as AD typically develops over decades, the data from post-mortem samples provides little mechanistic insights into how HNE or Aβ can alter NEP. Recently, Shinall et al. reported that recombinant NEP could be oxidatively inactivated (Shinall et al. 2005), which prompted us to explore whether HNE or Aβ could inactivate NEP in cultured cells. The data in this study show that exogenous HNE mediates NEP modification in a concentration-dependent manner which is associated with increased Aβ accumulation in culture media. These results, along with prior analysis of human brain tissue, implicate NEP oxidation as a possible cause of Aβ accumulation in AD brain.
Real-time RT-PCR indicated that NEP mRNA level was down-regulated at 6 hour which rebounded by 12 hours after HNE treatment. Western blotting did not show statistically significant changes in NEP protein levels. These data imply that NEP mRNA expression is more sensitive than protein to HNE treatment. The up-regulation of NEP mRNA may reflect compensation to reduced NEP (protein levels and catalytical activity) induced by HNE modifications. In addition, the non-significant alteration of NEP protein level at 24 h after HNE treatment may also reflect the consequences of up-regulation of NEP mRNA. These results suggest that NEP has a prolonged, in vitro half-life (>12h) and that NEP gene expression is sensitive to both HNE and Aβ, but in temporally distinct ways.
We also evaluated if HNE adduction altered NEP activity. Vmax, and Km revealed that NEP activity in SH-SY5Y cells followed Michealis-Menten kinetics, and demonstrated a hyperbolic dependence of v (velocity) on substrate concentration. The Km of NEP after HNE treatment of cell lysates was significantly increased when compared to control (Table 1), which implies that substrate affinity was decreased. The Vmax was unchanged in HNE incubated cells compared to controls, consistent with unchanged NEP concentration. The Lineweaver-Burk double-reciprocal plots are consistent with competitive inhibition by exogenous HNE treatment (data not shown). Overall, these kinetic parameters suggest a loss of enzymatic activity after HNE adduction, possibly by HNE mediated active site modification.
Unlike HNE treatment, Aβ up-regulated both NEP mRNA and protein levels (Figure 1B and Figure 2). Despite increased HNE adduction, there were no significant differences in NEP Km between control and Aβ peptide-treated cells (Table 1). However, Vmax tended to increase in the Aβ treated groups. These results are consistent with the double-reciprocal plots of Aβ versus HNE treated cells (Figure 6). Alternatively, Aβ induced HNE modifies NEP at a different intracellular location than exogenous HNE, accounting for dissimilar changes in enzymatic activity. Despite these differences, the specific activity of NEP showed reductions after either HNE or Aβ treatments. Detection of NEP protein and activity from the same samples by using ELISA and immunocaptured activity assay indicated that NEP activities are lower than the protein levels not only in HNE but also in Aβ treatments, even though Aβ actually increased the NEP protein level. The results are thus consistent with the in vivo inactivation of NEP observed in AD (Russo et al, 2005; Sakai et al, 2004). At this time, the mechanism for NEP upregulation is unknown. Whether this occurs early in vivo during early, evolving AD is also unknown. Since there are total of 70 amino acid residues including cysteine (C) (Esterbauer et al. 1991), histidine (H) (Uchida and Stadtman 1992, 1993) and lysine (K) (Szweda et al. 1993; Uchida and Stadtman 1993) in NEP could potentially be modified by HNE, it is very likely that synthetic HNE added to the cultured medium, which is at much higher concentrations, and HNE induced by Aβ1-42 modified NEP at the different percentage of the total NEP protein in any single cell. It is also possible that a single NEP molecule could be modified at the different extent under different pathophysiological conditions, which may affect NEP’s activity at the different level. There are several ongoing studies to explore this question in this laboratory.
Previous studies indicated that Aβ increase the production of free radicals by neurons (Butterfield et al. 2001; Butterfield and Lauderback 2002; Canevari et al. 2004; Crouch et al. 2008). Consistent with previous reports (Mark et al. 1997), we also show that Aβ induced HNE production within 24 hours. As seen with exogenous HNE treatment, Aβ increased HNE-NEP conjugates as measured by immunoprecipitation - western blotting and double immunofluorescence staining. Interestingly, acute treatment with Aβ peptide significantly induced NEP mRNA and protein, which was different from the findings in AD brain (Sakai et al. 2004; Russo et al. 2005). In AD transgenic mice (TgCRND8), which overexpress human mutant APP (KM670/671NL+V717F), Aβ deposition correlated with total neprilysin immunoreactivity. While the relative NEP signals were generally greater in the transgenic than in control mice, NEP was localized to and surrounded a subpopulation of plaques (Sato et al. 1991). This suggests that NEP may be induced as a consequence of Aβ deposition as we observed here in vitro. Similarly, human postmortem brains showed slightly increased total NEP in mild cognitive impairment (MCI) compared to age-matched normal control (Wang et al. 2003; Wang et al. 2005). Results from this study showed that specific NEP activities were lower in both HNE- and Aβ-treated cells, and indicated that oxidative modifications demonstrated by the increased ratio of HNE/NEP, decreased Aβ-catabolic activity might be contribute, at least partly, to the reduced Aβ cleavage and enhanced accumulation during the AD pathogenesis. The experiments on cell viability after the treatments with increasing concentrations of HNE or Aβ performed along with other experiments reported in this manuscripts showed that there was a significant decrease in overall cell and neurite number as the concentration of HNE or Aβ was increased. The cells lost neurites, rounded and detached from the plate. Cell viability as determined by MTT reduction was markedly decreased after exposure to HNE or Aβ, consistent with cell death (data not shown). Although both HNE and Aβ are known to be toxic to cultured neuronal cells, it is possible that other mechanisms also involved in neuronal cell death induced by Aβ in addition to the induction of HNE.
This work is supported by NIH grants AG025722 and AG029972 (to DSW), and an Alzheimer Association Grant IIRG-08-90524 (to DSW), and the start fund from the Department of Pathology and Laboratory Medicine, University of Wisconsin and Public Health, Madison, Wisconsin (to DSW).