(E)-2-Methoxy-4-(3-(4-methoxyphenyl) prop-1-en-1-yl) Phenol Ameliorates LPS-Mediated Memory Impairment by Inhibition of STAT3 Pathway
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Alzheimer’s disease (AD) is pathologically characterized by an excessive accumulation of amyloid-beta (Aβ) fibrils within the brain. We tested the anti-inflammatory and anti-amyloidogenic effects of (E)-2-methoxy-4-(3-(4-methoxyphenyl) prop-1-en-1-yl) phenol (MMPP), a selective signal transducer and activator of transcription 3 (STAT3) inhibitor. We examined whether MMPP (5 mg/kg in drinking water for 1 month) prevents amyloidogenesis and cognitive impairment on AD model mice induced by intraperitoneal LPS (250 μg/kg daily 7 times) injections. Additionally, we investigated the anti-neuroinflammatory and anti-amyloidogenic effect of MMPP (1, 5, and 10 μg/mL) in LPS (1 μg/mL)-treated cultured astrocytes and microglial BV-2 cells. MMPP treatment reduced LPS-induced memory loss. This memory recovery effect was associated with the reduction of LPS-induced inflammatory proteins; cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) as well as activation of microglial cells and astrocytes in the brain. Furthermore, MMPP reduced LPS-induced β-secretase and Aβ generation. In in vitro study, LPS-induced expression of inflammatory proteins and amyloidogenic proteins was decreased in microglial BV-2 cells and cultured astrocytes by MMPP treatment. Moreover, MMPP treatment suppressed DNA binding activities of the activation of STAT3 in in vivo and in vitro. These results indicated that MMPP inhibits LPS-induced amyloidogenesis and neuroinflammation via inhibition of STAT3.
KeywordsAlzheimer’s disease Neuroinflammation Amyloidogenesis Signal transducer and activator of transcription 3
Alzheimer’s disease (AD) is a chronic neurodegenerative disease in people over 65 years old. Although there are many causes for AD, the main cause is the accumulation of beta-amyloid (Aβ) which is the most toxic to brain cells. Aβ peptides are generated from amyloid precursor protein (APP) by β-site APP-cleaving enzyme 1 (BACE1) and γ-secretase. BACE1 cleaves the APP, producing a soluble APP fragment (sAPPβ) and a carboxy-terminal 99 amino acid (C99) protein. C99 is then cleaved within the membrane by γ-secretase and generates Aβ and APP intracellular domain (AICD) (Gu et al. 2015; Holsinger et al. 2002). Additionally, Aβ molecules can form flexible soluble oligomers which may exist in several forms (Schnabel 2010). Misfolded oligomers cause cell death of brain (Pulawski et al. 2012).
Lipopolysaccharide (LPS), an endotoxin isolated from gram-negative bacteria, can induce neuronal damage and inflammatory responses (Qin et al. 2007). Our and other previous studies have proved that memory impairment and amyloidogenesis can be induced by systemic injections of LPS in in vivo and in vitro (Lee et al. 2008; Hauss-Wegrzyniak et al. 1998; DiCarlo et al. 2001; Gu et al. 2015). Other study also demonstrated that LPS administered into brain could induce amyloidogenesis and neuroinflammation (Biesmans et al. 2013; Choi et al. 2012; Noh et al. 2014; Chen et al. 2008). LPS induces accumulation of Aβs in both the cerebral cortex and hippocampus through increased β- and γ-secretase activities accompanied with the increased expression of APP, C99 and generation of Aβ as well as activation of astrocytes and microglia (Sheng et al. 2003; Pop et al. 2012; Henry et al. 2009). In a neurodegenerative disease, microglial cells and astrocytes are activated (Madeddu et al. 2015). LPS has been widely used to establish an experimental model of glial activation (Sola et al. 2002). LPS also augmented microglia activation in the central nervous system and accelerated the progression of a neurodegenerative disease (Masocha 2009; Qin et al. 2007). Activated astrocytes expressing glial fibrillary acidic protein (GFAP) are closely associated with AD pathology such as amyloid depositions and, in practice, increased amounts of GFAP were detected in the frontal cortex of AD patients (Korolainen et al. 2005; Cotter et al. 2001). During a neurological disease, members of the activation of signal transducer and activator of transcription (STAT) family of transcription factor have critical roles in inflammatory reactions through regulating many proteins and cytokines involved in neuroinflammation (Ban et al. 2014; Song et al. 2014). In the pathogenesis of AD, activation of the STAT3 signaling pathway has a critical role because STAT3 is associated with cytokine signaling during neuronal differentiation and inflammation (Wan et al. 2010). It was also reported that STAT3 is activated and elevated in hippocampal slices taken postmortem from AD patients and the brains of AD mouse models (Wan et al. 2010). STAT3-mediated transcriptional control of BACE1 has implications for AD pathogenesis through the elevation of Aβ generation (Wen et al. 2008). It is believed that interfering with the signaling network of STAT3 activation could be an effective approach in the treatment for AD by decreasing the level of Aβ gene expression (Song et al. 2014; Carret-Rebillat et al. 2015). It has been reported that several agents such as thiacremonone (Song et al. 2014; Yun et al. 2016), 2,4-bis(p-hydroxyphenyl)-2-butenal (Jin et al. 2013), ent-Sauchinone (Song et al. 2014), 4-O-Methylhonokiol (Lee et al. 2012b) decreased β-secretase activity through the inhibiting STAT3 activity in AD model.
In our previous study, we found that the significant anti-inflammatory properties of (E)-2, 4-bis(p-hydroxyphenyl)-2-butenal (BHPB) as inhibiting STAT3 activation in arthritis (Ban et al. 2014), cancer (Cho et al. 2014) and AD (Jin et al. 2013). Derivative of BHPB, 2,4-bis(4-hydroxyphenyl)but-2-enal diacetate (HPBD) also showed anti-neuroinflammatory and anti-amyloidogenic effects (Kim et al. 2014). However, these chemicals have fatal disadvantages such as instability of structure to use as a drug and weakened binding affinity to STAT3. The upgraded BHPB analogue, (E)-2-methoxy-4-(3-(4-methoxyphenyl) prop-1-en-1-yl) phenol (MMPP) is designed with modification of the conjugated α,β-unsaturated aldehyde moiety and protection of phenolic alcohols to various ethers. It can strongly bind to STAT3 through a direct molecular interaction with the hydroxyl residue in the core fragment (CF) of STAT3, so it can inhibit activation of STAT3. Furthermore, we carried out an In silico toxicology and ADME (absorption, distribution, metabolism, and extraction) evaluation previously by using computational ADME QSAR models, preADMET (http://preadmet.bmdrc.org) and StarDrop (http://www.optibrium.com/stardrop/stardrop-features.php), to predicted the ADME of MMPP (Son et al. 2016). Blood–Brain Barrier (BBB) penetration is represented as BB = [Brain]/[Blood], where [Brain] and [Blood] are the steady-state concentration of radiolabeled compounds in brain and peripheral blood. It was predicted that MMPP shows higher value with 0.92, which suggest that MMPP could penetrates easily to BBB (the value 1 means that 100% of compound can penetrate BBB). We therefore investigated whether MMPP suppresses LPS-triggered inflammatory responses and amyloidogenesis in both in vitro and in vivo.
Materials and Methods
The experimental protocols were carried out according to the guidelines for animal experiments of Institutional Animal Care and Use Committee (IACUC) of Laboratory Animal Research Center at Chungbuk National University, Korea (CBNUA-929-16-01). All efforts were made to minimize animal suffering, and to reduce the number of animals used. All mice were housed in three mice per cage with automatic temperature control (21–25 °C), relative humidity (45–65%), and 12 h light–dark cycle illuminating from 08:00 a.m. to 08:00 p.m. Food and water were available ad libitum. They were fed pellet diet consisting of crude protein 20.5%, crude fat 3.5%, crude fiber 8.0%, crude ash 8.0%, calcium 0.5%, phosphorus 0.5% per 100 g of the diet (collected from Daehan Biolink, Chungcheongbuk-do, Korea). During this study, all mice were specially observed for the normal body posture, piloerection, ataxia, urination, etc., 2 times per day.
To synthesize MMPP, 4-Iodo-2-methoxyphenol (500 mg, 2.0 mmol, Sigma-Aldrich) and 4-allylanisole (296.4 mg, 2.0 mmol, Sigma-Aldrich) were added with triphenylphosphine (105 mg, 0.4 mmol), Pd(OAc)2 (44.9 mg, 0.2 mmol), and tributylamine (451 μL, 1.9 mmol) in a 25-mL round bottom flask and the reaction mixture was stirred for 2 h at 45 °C under argon atmosphere. The product was purified by flash silica gel chromatography using hexane and ethyl acetate (3:1 mixture v/v) as the mobile phase. Reduction of the alkene or the aldehyde of α, β -unsaturated aldehyde moiety resulted in stable compounds as protecting the phenolic alcohol from ether.
Eight-to-ten week-old-male imprinting control region (ICR) mice (Hajinbiotech, Gyeonggi-do, Korea) were maintained and handled in accordance with the humane animal care and use guidelines of Korean FDA. To induce neuroinflammatory cognitive impairment model, LPS (250 μg/kg) was administered intraperitoneally (Lee et al. 2013a). Previous studies revealed that LPS injection caused amyloidogenesis and memory loss in mice brain through NF-κB activation (Lee et al. 2012a; Choi et al. 2012; Lee et al. 2013b; Fan et al. 2014). Also, STATs have been involved in amyloidogenesis through the modulation of secretases (Hashimoto et al. 2005). There are three groups: (I) Control group, (II) LPS group, and (III) MMPP + LPS group where each group was assigned 10 mice. The MMPP was given to (III) group in drinking water daily at a dose of 5 mg/kg for 4 weeks. Intraperitoneal (i.p.) injection of LPS (250 μg/kg) was administered except for the control group on the 4th week for 7 days. The doses of MMPP are referred to in a previous study (Jin et al. 2013). The behavioral tests of learning and memory capacity were then assessed using three tests (water maze, probe and passive avoidance test). The water maze test was performed even days after the MMPP and LPS administration. The probe test was performed one day after the water maze test. The passive avoidance test was performed one day after the probe test.
Morris Water Maze
The water maze test is also a commonly accepted method for memory test, and we performed this test as described by Morris et al. (Morris 1984). Maze testing was fulfilled by the SMART-CS (Panlab, Barcelona, Spain) program and equipment. A circular plastic pool (height: 35 cm, diameter: 100 cm) was filled with squid ink water kept at 22–25 °C. An escape platform (height: 14.5 cm, diameter: 4.5 cm) was submerged 1–1.5 cm below the surface of the water in position. On training trials, the mice were placed in a pool of water and allowed to remain on the platform for 120 s and were then returned to the cage. The mice that did not find the platform within 60 s were placed on the platform for 10 s at the end of trial. The mice that did find the platform and stayed on it for 3 s within the 60 s were placed on the platform for seven more seconds at the end of trial. These trials were performed on a single platform and at two rotational starting positions. Escape latency and escape distance of each mouse were monitored by a camera above the center of the pool connected to a SMART-LD program (Panlab, Barcelona, Spain).
To assess memory retention, a probe test was performed 24 h after the water maze test. The platform was removed from the pool which was used in the water maze test, and the mice were allowed to swim freely. The swimming pattern of each mouse was monitored and recorded for 60 s using the SMART-LD program (Panlab). Retained spatial memory was estimated by the time spent in the target quadrant area.
Passive Avoidance Performance Test
The passive avoidance test is generally accepted as a simple method for testing memory. The passive avoidance response was determined using a “step-through” apparatus (Med Associates Inc, Vermont, USA) that is divided into an illuminated compartment and a dark compartment (each 20.3 × 15.9 × 21.3 cm) adjoining each other through a small gate with a grid floor, 3.175 mm stainless steel rods set 8 mm apart. On the first day, the mice were placed in the illuminated compartment facing away from the dark compartment for the training trial. When the mice moved completely into the dark compartment, it received an electric shock (0.45 mA, 3 s duration). Then, the mice were returned to their cage. One day after training trial, the mice were placed in the illuminated compartment and the latency period to enter the dark compartment defined as “retention” was measured. The time when the mice entered into the dark compartment was recorded and described as step-through latency. The retention trials were set at a cutoff time limit of 3 min.
Brain Collection and Preservation
After behavioral tests, mice were perfused with phosphate-buffered saline (PBS, pH 7.4) with heparin under inhaled CO2 anesthetization. The brains were immediately removed from the skulls and divided into left brain and right brain. One stored at −80 °C, the other were fixed in 4% paraformaldehyde for 72 h at 4 °C and transferred to 30% sucrose solutions.
Astrocytes and Microglial BV-2 Cells Culture
Astrocytes were prepared from the cerebral cortex of rat embryos (E18). After the skull was cut and the skin was opened, the brain was released from the skull cavity. After washing with PBS, the cerebrum was separated from the cerebellum and brain stem, and the cerebral hemispheres were separated from each other by gently teasing along the midline fissure with the sharp edge of forceps. The meninges were gently peeled from the individual cortical lobes and the cortices were dissociated by mechanical digestion [using the cell strainer (BD Bioscience, Franklin Lakes, NJ, USA)]. The resulting cells were centrifuged (1500 rpm, 5 min), resuspended in serum-supplemented culture media, and plated into 100 mm dishes. The cells were seeded on culture flasks T-75 and incubated in Dulbecco’s modified eagle medium (DMEM)/F-12 (Invitrogen, Carlsbad, CA) containing 10% fetal bovine serum (FBS) (Invitrogen). The culture medium was replaced every 3 days thereafter. After 14 days, the cultures became confluent and loosely attached microglia and oligodendrocyte precursor cells were removed from the cell monolayer using shaking incubator (37 °C, 350 RPM, 2–4 h). Astrocytes were subsequently detached using trypsin–EDTA and plated into 100 mm cell culture dishes. The percentage of astrocytes in our culture system is more than 95%. Microglial BV-2 cells were maintained with serum-supplemented culture media of DMEM supplemented with FBS (10%) and antibiotics (100 units/mL). The microglial BV-2 were incubated in the culture medium in a humidified incubator at 37 °C and 5% CO2. The cultured cells were treated with several concentrations (1.0, 5.0 10.0 μg/mL) of MMPP, 2 h before LPS (1 μg/mL) addition, and astrocytes were treated in a basal medium that contains 1% FBS. The cells were harvested after 24 h.
After being transferred to 30% sucrose solutions, brains were cut into 20 μm sections by using a cryostat microtome (Leica CM 1850; Leica Microsystems, Seoul, Korea). After two washes in PBS (pH 7.4) for 10 min each, endogenous peroxidase activity was quenched by incubating the samples in 3% hydrogen peroxide in PBS for 20 min, and then two washes in PBS for 10 min each. The brain sections were blocked for 1 h in 5% bovine serum albumin (BSA) solution, and incubated overnight at 4 °C with a mouse polyclonal antibody against GFAP (1:300; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), inducible nitric oxide synthase (iNOS) (1:300; Novus Biologicals, Inc., Littleton), a rabbit polyclonal antibody against cyclooxygenase-2 (COX-2) (1:300; Cell Signaling Technology, Inc., Beverly, MA, USA), and a goat polyclonal antibody against ionize calcium-binding adapter molecule 1 (Iba-1) (1:300; Abcam, Inc., Cambridge, MA, USA). After incubation with the primary antibodies, brain sections were washed twice in PBS for 10 min each. After washing, brain sections were incubated for 1–2 h at room temperature with the biotinylated goat anti-rabbit or goat anti-mouse or donkey anti-goat IgG-horseradish peroxidase (HRP) secondary antibodies (1:500; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA). Brain sections were washed thrice in PBS for 10 min each, and visualized by a chromogen DAB (Vector Laboratories) reaction for up to 10 min. Finally, brain sections were dehydrated in ethanol, cleared in xylene, mounted with Permount (Fisher Scientific, Hampton, NH), and evaluated on a light microscopy (Microscope Axio Imager.A2, Carl Zeiss, Oberkochen, Germany) (× 50 and × 200). We investigated the region of brain from CA3 and DG region in hippocampus for anatomical studies. CA3 and DG network is the most critical for contributing to memory storage and retrieval of memory sequences.
The fixed cells and brain sections were exposed to the following primary antibodies: GFAP (1:300, Santa Cruz Biotechnology Inc. Santa Cruz, CA, USA), Iba-1 (1:300, Abcam, Inc., Cambridge, MA, USA), and Aβ1–42 (1:300, Abcam ab10148, Inc., Cambridge, MA, USA) at room temperature for 2 h. The Aβ1–42 antibody is reactive with Aβ1–42 and does not cross-react with Aβ1–42, full-length APP, sAPP beta or sAPP alpha. After incubation, the cells were washed twice with ice-cold PBS and incubated with an anti-rabbit or mouse or goat secondary antibody conjugated to Alexa Fluor 488 or 568 nm (Invitrogen-Molecular Probes, Carlsbad, CA) at room temperature for 1 h. Immunofluorescence images were acquired using an inverted fluorescent microscope Zeiss Axiovert 200 M (Carl Zeiss, Thornwood, NY) (× 200). We investigated the region of brain from CA3 and DG region in hippocampus for anatomical studies. CA3 and DG network is the most critical for contributing to memory storage and retrieval of memory sequences.
Thioflavin S Staining
After being transferred to 30% sucrose solutions, brains were cut into 20 μm sections by using a cryostat microtome (Leica CM 1850; Leica Microsystems, Seoul, Korea). After washes in distilled water for 5 min, brain sections were transferred to gelatin-coated slide and placed in 1% thioflavin S (Thioflavin S, Sigma, St Louis, MO, USA) for 5 min. Brain sections were then washed in distilled water and then dehydrated through ascending grades of ethanol, 50, 70, 90, and 100% ethanol for 2 min in each grade. The sections were then mounted in a mounting medium (Fluoromount™ Aqueous Mounting Medium, Sigma, St Louis, MO, USA). The thioflavin S staining was examined using a fluorescence microscope (Axio Observer A1, Carl Zeiss, Oberkochen, Germany) (× 100). We investigated the region of brain from CA3 and DG region in hippocampus for anatomical studies. CA3 and DG network is the most critical for contributing to memory storage and retrieval of memory sequences.
Measurement of Aβ1–42
Lysates of brain tissue were obtained through protein extraction buffer containing protease inhibitor. Aβ1–42 levels were determined using each specific mouse amyloid-beta peptide 1-42 ELISA Kit (CUSABIO, CSB-E10787 m). Protein was extracted from brain tissues using a protein extraction buffer (PRO-PREPTM, Intron Biotechnology, Korea), incubated on ice for 1 h and centrifuged at 13,000 × g for 15 min at 4 °C. In brief, 100 μL of sample was added into a precoated plate and incubated for 2 h at 37 °C. After removing any unbound substances, a biotin-conjugated antibody specific for Aβ1–42 was added to the wells. After washing, avidin-conjugated HRP was added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution was added to the wells and color developed in proportion to the amount of Aβ1–42 bound in the initial step. The color development was stopped and the intensity of the color was measured.
Assay of β-secretase Activities
β-secretase activity in the mice brains was determined using a commercially available β-secretase activity kit (Abcam, Inc, Cambridge, MA, USA). Solubilized membranes were extracted from brain tissues using β-secretase extraction buffer, incubated on ice for 1 h and centrifuged at 5000 × g for 10 min at 4 °C. The supernatant was collected. A total of 50 μL of sample (total protein 100 μg) or blank (β-secretase extraction buffer 50 μL) was added to each well (used 96-well plate) followed by 50 μL of 2 × reaction buffer and 2 μL of β-secretase substrate incubated in the dark at 37 °C for 1 h. Fluorescence was read at excitation and emission wavelengths of 335 and 495 nm, respectively, using a fluorescence spectrometer (Gemini EM, Molecular Devices, California, USA).
Nuclear Extraction and Gel Mobility Shift Assay
Gel mobility shift assay was conducted using a slight modification of a previously described method (Lee et al. 2011). In brief, 10 μg of nuclear protein of astrocytes, microglial BV-2 cells and brain tissues was incubated in 25 μL of total volume of incubation buffer (10 mmol/L Tris, pH 7.5, 100 mmol/L NaCl, 1 mmol/L dithiothreitol, 4% glycerol, 80 mg/L salmon sperm DNA) at 4 °C for 15 min followed by another 20 min incubation with 9.25 mBq [-32P] ATP-labeled oligonucleotide containing STAT3 binding site at room temperature. The DNA–protein binding complex was electrophoretically resolved on a 5% non-denatured polyacrylamide gel at 150 volts for 90 min. The gels were dried and autoradiographed using Kodak MR film at −80 °C overnight.
In in vivo and in vitro study, for comparing the expression of protein levels through Western blotting, we selected and used 3 of 10 mice brain from each group. An equal amount of total protein (20 μg) was resolved on 8–15% sodium dodecyl sulfate polyacrylamide gel and then transferred to a nitrocellulose membrane (Hybond ECL; Amersham Pharmacia Biotech, Piscataway, NJ, USA). The membranes were blocked for 1 h in 5% skim milk solution, and incubated overnight at 4 °C with specific antibodies. To detect target proteins, specific antibodies against C99 (1:1000, EMD Millipore, Billerica, MA, USA), APP, iNOS (1:1000, Novus Biologicals, Inc., Littleton), BACE1, Iba-1 (1:1000, Abcam, Inc., Cambridge, MA, USA), COX-2 (1:1000, Cell Signaling Technology, Inc., Beverly, MA, USA), GFAP, STAT3, p-STAT3, β-actin (1:1000, Santa Cruz Biotechnology Inc. Santa Cruz, CA, USA) were used. The blots were then incubated with the corresponding conjugated goat anti-rabbit or goat anti-mouse or donkey anti-goat IgG-HRP (1:5000; Santa Cruz Biotechnology Inc. Santa Cruz, CA, USA) secondary antibodies. Immunoreactive proteins were detected with an enhanced chemiluminescence Western blotting detection system. The relative density of the protein bands was scanned and quantified by ImageJ (Wayne Rasband, National Institutes of Health, Bethesda, MD) was used.
Astrocytes and microglial BV-2 cells were plated at a density of 5 × 105 cells/well in 6-well plates per 2 mL medium for 24 h. After removing the culture medium, the cells were then treated with LPS (1 μg/mL) and MMPP (1, 5, 10 μg/mL) per 2 mL medium for 24 h. The nitrite in the supernatant was assessed using a NO detection kit (iNtRON Biotechnology, Seongnam, Korea), according to the manufacturer’s instructions. Finally, the resulting color was assayed at 520 nm using a microplate absorbance reader (VersaMax ELISA, Molecular Devices, California, USA).
RNA Isolation and Quantitative Real-Time RT-PCR
Cell RNA was isolated from homogenized microglial BV-2 cells and primary cell cultured astrocytes using RiboEX (Gene All, Seoul, Korea), and total RNA (0.2 μg) was reverse-transcribed into cDNA according to the manufacturer’s instructions using Applied Biosystems (Foster City, CA, USA). For the quantitative, real-time, reverse transcriptase polymerase chain reaction (PCR) assays, the linearity of the amplifications of IL-6, IL-10, and β-actin cDNAs was established in preliminary experiments. All signal mRNAs were normalized to β-actin mRNA. cDNAs were amplified by real-time PCR in duplicate with QuantiNova SYBR green PCR kit (Qiagen, Valencia, CA, USA). Each sample was run with the following primer sets: IL-6, 5′-GAGGATACCACTCCCAACAGACC-3′ (sense), 5′-AAGTGCATCATCGTTGTTCATACA-3′ (antisense); IL-10, 5′-TCTGAGCCACTCACATCTGC-3′ (sense), 5′-TCAGGGGAACTGCTAGTGCT-3′ (antisense); β-actin: 5′-TGGAATCCTGTGGCATCCATGAAAC-3′ (sense), 5′-TAAAACGCAGCTCAGTAACAGTCCG-3′ (antisense).
The region of Mus musculus STAT3 was amplified by PCR using full-length Mus musculus STAT3 cDNA as a template. The purified PCR products were double-digested with EcoRI and XhoI and then subcloned into the pcDNA3.1 vector. The pcDNA3.1 plasmid contains a cytomegalovirus promoter, pUC origin, and ampicillin-resistance gene. STAT3 (T456A) mutagenesis was generated by Cosmogenetech Co. (Seoul, Korea) and the mutant was systematically checked by sequencing. RAW264.7 cells were plated at a density of 1 × 105 cells per 24-well plate. After 24 h of growth to 90% confluence, the cells were transfected with mutant STAT3 plasmid (T456A; T, a core amino acid of DNA binding domain was replaced with un related amino acid A) using Lipofectamine LTX & PLUS (Invitrogen Co., Carlsbad, CA, USA) in OPTI-MEM media (Invitrogen) according to the manufacturer’s instructions.
For the measurement of the image data, ImageJ (Wayne Rasband, National Institutes of Health, Bethesda, MD) was used. Group differences were analyzed by one-way ANOVA followed by bonferroni’s post hoc analysis using GraphPad Prism 5 software (Version 5.02, GraphPad software, Inc., La Jolla, USA).
MMPP Treatment Inhibits Memory Impairment in LPS-Treated Mice
MMPP Treatment Inhibits Aβ Accumulation and Amyloidogenesis in Brains of LPS-Treated Mice
MMPP Treatment Downregulates STAT3 Activation in LPS-Treated Mice Brain
MMPP Reduces Neuroinflammation in Brain of LPS-Treated Mice
To investigate the activation of astrocytes and microglia cells as well as neuroinflammation, we performed immunohistochemistry (IHC) and Western blotting to detect the expression of GFAP (a marker of astrocyte activation), Iba-1 (a marker of microglia cell activation) and inflammatory proteins (iNOS and COX-2) in the brain. The GFAP-reactive cell number and Iba-1-reactive cell number were reduced in the mice brains with the treatment of MMPP compared to those in LPS-injected mice which showed much higher numbers of cells reactive for these marker proteins compared to non-treated mice brains (Fig. 4c). The expression of GFAP and Iba-1 was also significantly decreased in the brains of MMPP-treated mice than LPS-injected mice brains (Fig. 4d). We also investigated the inhibitory effect of MMPP in neuroinflammation; the expression of iNOS and COX-2 were determined. Treatment of LPS elevated the expression of inflammatory proteins (iNOS and COX-2), GFAP and Iba-1, but the expressions were significantly reduced by the treatment of MMPP (Fig. 4e).
MMPP Inhibits Amlyloidogenesis and Neuroinflammation in Cultured Astrocytes and Microglial Cells
MMPP Suppresses STAT3 Signaling by Interacting with STAT3 Core Fragment of DNA Binding Domain
Accumulating epidemiological studies have suggested that neuroinflammatory responses may contribute to the progression of AD (Eikelenboom et al. 2002). The pathological hallmarks of neuroinflammation including marked astrogliosis, elevated release of proinflammatory mediators and cytokines appear in AD patients (Lee et al. 2012a). Our and other studies demonstrated that systemic injections of LPS-induced memory impairment through progressive neuroinflammation and amyloidogenesis (Lee et al. 2008; Lim et al. 2000; Hwang et al. 2016). We have demonstrated that several anti-inflammatory compounds such as 4-O-methylhonokiol, thiacremonone, obovatol and 2,4-bis(p-hydroxyphenyl)-2-butenal improved memory functions in AD animal models (Choi et al. 2012; Jin et al. 2013; Lee et al. 2012b; Yun et al. 2016).
In our recent study, we found that MMPP has strongest STAT3 DNA binding activities by luciferase activity in Raw 264.7 cells, and strongest binding affinity (−8.2 kcal/mol). Moreover, MMPP does not show any toxicities with suitable drug-likeness properties evaluated by computational ADME QSAR models using preAPMET and StarDrop soft program. MMPP exhibits significantly advantageous drug-likeness. (E)-2,4-bis(p-hydroxyphenyl)-2-butenal showed plausible mutagenicity in vivo and chromosome damage in vitro, while MMPP did not exhibit any of these mutagenic effects. (E)-2,4-bis(p-hydroxyphenyl)-2-butenal tested negative for other predicted toxicities except hepatotoxicity. However, MMPP treatment (5 mg/kg) for 3 weeks did not show hepatotoxic effects and MMPP showed better aqueous solubility, human intestinal absorption, and skin permeability. Furthermore, MMPP has multiple pharmacological properties against arthritis, neuroinflammation, and tumor growth, thus it is possible that MMPP could be a candidate compound to be developed as a drug (Zheng et al. 2017; Park et al. 2017).
It is notably reported that elevation of STAT3 phosphorylation is evident in postmortem samples of AD brains (Wan et al. 2010). STAT3 activates the transcription of BACE1, APP, presenilin-1 and γ-secretase and therefore increases production of Aβ1-42 because STAT3 transcriptionally regulates the mRNA levels of both BACE1 and presenilin-1 (Chiba et al. 2009; Liu et al. 2013). It was also reported that BACE1 transcription can be increased by inflammatory responses with activation of astrocytes and microglia induced by LPS as well as Aβ1-42 (Sambamurti et al. 2004). It is noteworthy that LPS could upregulate neuroinflammation in astrocytes and microglia through activation of STAT3. Activated astrocytes and microglia are closely associated with amyloid plaques in AD. Additionally, IL-6 and IL-10 are known for signaling via activation of transcription factor STAT3 (Niemand et al. 2003). It was also reported that increased IL-6 brain showed that severe cognitive impairments and behavioral deficits with neuronal loss (Wei et al. 2012). Furthermore, STAT3 has central roles in anti-inflammatory pathway, mediating IL-10 signals. These findings indicate that strategies to reduce IL-6 and IL-10 production may be particularly valuable for protecting the CNS disorders including AD. Our results indicate that MMPP could be a potential drug to control STAT3 activation and decrease production of neuroinflammatory cytokines including IL-6 and IL-10. Thus, inhibitory effects of MMPP on neuroinflammation and amyloidogenesis could be associated with its memory recovery effect, and targeting STAT3 is significantly contributing to these benefits. We previously found that MMPP directly binds to the DNA binding domain of STAT3 demonstrated by docking model, pull down assay as well as surface plasmon resonance (SPR) analysis. Moreover, we verified that the inhibitory effect of MMPP was abolished in the macrophages transiently transfected DNA binding domain mutant (T456A) plasmid. These data further demonstrated the significance of STAT3 in the biological effects of MMPP. Similar to our present data, other studies, as well as ours, have demonstrated that several compounds such as ent-Sauchinone (Song et al. 2014), 2,4-bis(4-hydroxyphenyl)-2-butenal diacetate (Kim et al. 2014), Kaempferol Glycosides (Yu et al. 2013) and Curcumin (Zhu et al. 2014) targeting STAT3 could be significant drugs for anti-amyloidogenesis and anti-inflammatory responses controlling the memory functions.
Dopenazil (Aricept®), Galantamine (Razadyne®) and Rivastigmine (Exelon®) are approved by the Food and Drug Administration (FDA) for treatment of AD as inhibiting the degradation of the neurotransmitter acetylcholine (Ach) (Pettenati et al. 2003; Farrimond et al. 2012). However, there are a number of AD patients undergoing various side effects by taking these drugs. For example, patients who are taking Aricept that overdose have experienced nausea, diarrhea, insomnia, and vomiting with gastrointestinal disorder. Furthermore, although AChE inhibitors help alleviate AD symptoms, they do not delay disease progression. Therefore, new therapeutic agents that block the disease-inducing mechanisms are essential (Yoo and Park 2012). Even though the mechanism of MMPP is different from FDA approved drugs, the improved toxicology of MMPP could be a promising candidate for treatment of AD. In addition, a combination of acetylcholinesterase inhibitor (AChEI) and inactivating the STAT3 pathway with MMPP treatment is a therapy of greater benefit in AD patients than taking AChEIs alone (Parsons et al. 2013; Park et al. 2013).
In conclusion, our findings demonstrate that MMPP has a potent therapeutic ability by inactivating STAT3 in LPS-treated mice AD model through inhibition of STAT3, which could result in the inhibition of Aβ accumulation by attenuating β-secretase activity. These findings suggest that one mechanism by which MMPP prevents anti-amyloidogenesis is due to a decrease in phosphorylation of STAT3. Thus, we suggest that MMPP could be useful for the treatment and/or prevention of AD.
This work is financially supported by the National Research Foundation of Korea [NRF] Grant funded by the Korea government (MSIP) (No. MRC, 2017R1A5A2015541), and by the Functional Districts of the Science Belt support program, Ministry of Science, ICT and Future Planning.
Compliance with Ethical Standards
Conflict of interest
The authors declare that they have no conflict of interest.
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