1. Introduction
Arterial thrombosis can cause cardiovascular diseases (CVDs), including myocardial infarction, atherosclerosis, ischemic stroke, venous thromboembolism, and peripheral artery diseases, which are the leading causes of mortality worldwide. When vascular subendothelial connective tissues are exposed due to injury, platelet adhesion and aggregation are critical events that aid platelet plug formation and halt bleeding (hemostasis). Although the main role of platelets is to prevent blood loss following tissue injury, platelets are responsible for pathogenic thrombus formation which causes vascular thromboembolic diseases [
1].
Collagen contained in the basement membrane induces a change in shape from discoid to spheroid with pseudopodic platelet projections. Classically, platelet activation is induced by collagen or soluble platelet agonists, leading to the activation of platelet adhesion receptors, mainly integrin α
IIbβ
3, which mediates platelet adhesion and aggregation [
2]. In resting platelets, integrin α
IIbβ
3 exists in a low activation state and is unable to interact with its specific ligands such as fibrinogen and fibronectin. Platelet activation stimulated by agonists induces a conformational change in integrin α
IIbβ
3, enabling it to bind to its ligands, thus resulting in the onset of platelet aggregation; this process is recognized as integrin α
IIbβ
3 inside-out signaling [
2]. Moreover, the binding of fibrinogen to directly activate integrin α
IIbβ
3 initiates a series of intracellular signaling events, such as the tyrosine phosphorylation of proteins and the reorganization of the cytoskeleton, which are referred to as outside-in signaling [
2]. These outside-in reactions, originating in integrin α
IIbβ
3 bound to fibrinogen, are required for maximal secretion, procoagulation, and clot retraction [
2].
Pterostilbene (PTE; trans-3,5-dimethoxy-4′-hydroxystilbene;
Figure 1A), a natural stilbenoid occurring in grapes and berries, is a dimethylated analog of resveratrol [
3]. PTE exhibits several remarkable pharmacological activities [
4] including antiaging, anticancer, anti-diabetes, and neuroprotection. In addition, Park et al. [
5] demonstrated that PTE inhibited the PDGF-BB-induced cell growth of vascular smooth muscle cells in rats through inhibition of the Akt-dependent pathway. Furthermore, PTE prevented atherosclerosis through regulation of the Nrf2-mediated TLR-4/MyD88/NF-κB pathway in rats [
6]. For antiplatelet activity, Messina et al. [
7] reported that PTE markedly diminishes collagen-stimulated platelet aggregation. Moreover, we observed that resveratrol exhibits potent antiplatelet activity through the inhibition of the p38 MAPK-phospholipase A
2 cascade, as described previously [
8]. Our initial screening exhibited that PTE (1–6 μM) is highly effective in inhibiting collagen-stimulated platelet aggregation in humans. However, few studies have reported the effects of PTE on platelet activation. Therefore, in this study, we elucidated PTE mechanisms underlying platelet activation both ex vivo and in vivo to support the scientific rationale for its clinical use.
3. Discussion
The results of this study showed that PTE resulted in high antiplatelet activity in humans. Plant-based polyphenols cause vasoprotection, antiangiogenesis, and antithrombosis in patients with CVDs [
12]. Resveratrol, a polyphenol derivative, exhibits valuable activity in controlling heart diseases [
13]. However, low oral bioavailability and rapid first-pass metabolism of resveratrol markedly affect its clinical application [
14]. In fact, the properties of poor bioavailability and rapid metabolism are common among polyphenols. By contrast, methylated polyphenols exhibit substantially higher intestinal absorption and enhanced hepatic stability [
15]. Thus, structural modifications of resveratrol that increase its bioavailability while preserving its beneficial activities are warranted. Structurally, PTE, a naturally occurring dimethyl ether analog of resveratrol, possesses better metabolic stability than resveratrol because it has only one hydroxyl group, whereas resveratrol has three hydroxyl groups (
Figure 1A). The dimethyl ether structure of PTE was suggested to increase membrane permeability and enhance its lipophilicity, resulting in better pharmacokinetic profiles than those of resveratrol [
16]. Therefore, the bioavailability and plasma levels of PTE were considerably higher than those of the equimolar doses of resveratrol, regardless of the dose or route of administration. The pharmacokinetics of PTE following the daily oral dosing of 56 mg/kg for 14 days in rats found that the blood concentration (Cmax) was approximated at 2550 ng/mL (~10 μM) [
17]. The result indicated that the concentration of 3.5 and 6 μM used in this antiplatelet study was reasonable, and can be reached in the circulation after dietary intake. Although normal PTE obtained from natural sources would be insufficient to achieve the required plasma concentration that can inhibit in vivo platelet activation, the long-term intake of sufficient natural food products or nutritional supplements is ideal for preventing atherothrombotic events; thus, PTE may serve as an innovative antithrombotic agent in humans because it exhibits high anti-platelet activity.
Platelets are activated by a variety of physiological stimuli (e.g., thrombin, collagen). In general, these agonists act through specific receptors or act by altering/instigating particular signal transduction pathways associated with other receptors. Thrombin is one of the most potent activators of platelets, and its role in promoting thrombus formation has been clearly established. Thrombin activates platelets through multiple cell-surface receptors, including the GP Ib/V/IX complex and the protease-activated receptors (PARs). Of the four known PAR isoforms, PAR1 and PAR4, are essential for thrombin-induced human platelet activation [
18]. Thrombin activates human platelets by cleaving and activating PAR1 and PAR4. In turn, these receptors activate Gq, G
12/13, and possibly the Gi family, which leads to the activation of phospholipase C, phosphoinositide 3-kinase, and the monomeric G proteins (i.e., Rho); the activation also causes an increase in cytosolic Ca
2+ concentration and inhibits cyclic AMP formation [
18,
19]. In addition, platelet adhesion is related to collagen. Platelets can adhere to multiple surfaces including cells and other adhesive proteins; however, initial adhesion is typically to the collagen surface. Collagen is found in the subendothelial space and within the tunica media (middle layer of blood vessels) and tunica adventitia (outermost layer of blood vessels). Therefore, collagen is the most important protein that can interact with platelets and induce activation responses. Apparently, all collagen receptors converge to the platelet tyrosine kinase signaling cascade, which promotes a transient increase in intracellular calcium, platelet aggregation (through integrin α
IIbβ
3), and granule secretion [
20]. Among platelet receptors known to directly interact with collagen, integrin α
2β
1 (GP Ia/IIa) and GP VI appear to play a key role and have recently gained the attention of researchers [
21]. GP VI is widely recognized as a requisite factor for platelet aggregate formation on a collagen surface under blood flow; integrin α
2β
1 is another collagen receptor on endothelial cells and platelets. GP VI belongs to a membrane of the immunoglobulin superfamily, which forms a complex with the Fc receptor γ-chain containing immunoreceptor tyrosine-based activation motifs and is phosphorylated by SFKs such as Fyn and Lyn [
22]. In turn, different pathways of protein phosphorylation regulate integrin α
IIbβ
3 activation through inside-out mechanisms. In the current study, PTE selectively inhibited platelet aggregation induced by collagen rather than that by thrombin, indicating that antiplatelet effects of PTE may interfered with the signal transduction pathway stimulated by collagen, but not by thrombin; however, more experiments are needed to verify the detailed mechanisms of PTE.
The fibrinogen–integrin α
IIbβ
3 binding belongs to a major component of activated platelets. Integrin α
IIbβ
3 undergoes conformational changes on activation, generating a unique and specific ligand-binding site for fibrinogen, von Willebrand factor, and fibronectin [
2]. PAC-1 reacts with the activation-induced conformational epitope of integrin α
IIbβ
3 [
23], and PAC-1 binding was markedly reversed by PTE treatment stimulated by collagen. In addition, platelets adhered to immobilized fibrinogen and platelet-mediated fibrin clot retraction are involved in integrin α
IIbβ
3 outside-in signaling [
2]. Integrin α
IIbβ
3-mediated signaling begins immediately after a fibrinogen molecule binds to the integrin α
IIbβ
3; this outside-in signaling results in the tyrosine phosphorylation of numerous proteins, such as SFK, FAK, and the cytoplasmic tail of integrin β
3 at Tyr
759, a process dependent on outside-in signaling and cytoskeleton reorganization [
2]. The critical role of integrin β
3 at Tyr
759 in platelets was demonstrated in vivo, and its mutation led to bleeding disorder and strongly affected clot retraction responses in vitro [
24]. FAK, a cytoplasmic tyrosine kinase located at focal adhesion points, plays a vital role in cytoskeleton regulation and integrin α
IIbβ
3 activity [
25]. Adhesion of platelets to immobilized fibrinogen requires FAK activation through integrin α
IIbβ
3, and, in turn, FAK activation requires autophosphorylation [
25]. In the current study, PTE noticeably abolished platelet adhesion and spreading and clot retraction as well as the phosphorylation of integrin β
3, Src, and FAK on immobilized fibrinogen in the absence of platelet agonists. Taken together, PTE potentially acts on integrin α
IIbβ
3 and blocks both integrin α
IIbβ
3-mediated inside-out and outside-in signaling. By contrast, we do not rule out the possibility that other, as yet unidentified mechanisms could be involved in the PTE-mediated inhibition of platelet activation.
Reactive oxygen species derived from platelet activation, such as hydrogen peroxide and hydroxyl radicals, play an important role in regulating platelet responses in collagen-mediated thrombus formation [
26]. Some of the hydrogen peroxide produced in platelets is converted into hydroxyl radicals, which acts as secondary signals that increase [Ca
2+]i levels during the initial phase of platelet activation [
26]. Begonja et al. [
27] reported that ROS produced in platelets significantly affected integrin α
IIbβ
3 activation. The results of our ESR analysis provide direct evidence that PTE scavenges hydroxyl radicals in human platelets. Thus, the PTE-mediated inhibition of thrombogenesis in vivo may involve scavenging free radical formation. After vascular endothelial cell injury, exposure to subendothelial collagen majorly triggers platelet adhesion and aggregation at the injury site, followed by vascular thrombosis. Animal models of vascular thrombosis are necessary to understand the effectiveness of test compounds in disease treatment. An ideal mouse model should technically be simple, quick in operation, and easily reproducible. In a vascular thrombotic mouse model [
28], mesenteric venules were continuously irradiated with fluorescein sodium throughout the experimental period, which severely damaged the endothelium, whereas treatment with 2 mg/kg PTE significantly extended the occlusion time. These data are consistent with the fact that platelet aggregation is a crucial factor causing vascular thrombosis. Therefore, PTE can be a potential natural compound for treating thromboembolic disorders.
4. Materials and Methods
4.1. Materials
PTE (>98%), collagen (type I), fibrinogen, heparin, fluorescein isothiocyanate (FITC)–phalloidin, 5,5-dimethyl-1 pyrroline N-oxide (DMPO), bovine serum albumin (BSA), aspirin, and thrombin were purchased from Sigma (St. Louis, MO, USA). An anti-integrin β3 monoclonal antibody (mAb) and anti-phospho-integrin β3 (Tyr759) polyclonal antibody (pAb) were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Anti-phospho-Src family (Tyr416), anti-phospho-Syk (Tyr525/526), and anti-phospho-FAK (Tyr397) mAbs and anti-Syk, anti-Src family, and anti-FAK pAbs were purchased from Cell Signaling (Beverly, MA, USA). The FITC-anti-human CD41/CD61 (PAC-1) mAb was obtained from BioLegend (San Diego, CA, USA). Anti-phospho-Fyn (Tyr530) pAb, anti-phospho-Lyn (Tyr497), anti-Fyn, and anti-Lyn mAbs were obtained from Abcam (Cambridge, UK). A Hybond-P polyvinylidene difluoride membrane, an enhanced chemiluminescence Western blotting detection reagent, horseradish peroxidase-conjugated donkey anti-rabbit immunoglobulin G (IgG), and sheep anti-mouse IgG were purchased from Amersham (Buckinghamshire, UK). PTE suspension was prepared in 0.1% dimethyl sulfoxide (DMSO) and stored at 4 °C.
4.2. Platelet Preparation and Aggregation Study
This study complied with the directives of the Helsinki Declaration and was approved by the Institutional Review Board of Taipei Medical University (N201812024). Informed consent was obtained from all human volunteers who participated in this study. Human platelets were washed as described previously [
29]. Blood was mixed with acid/citrate/glucose (9:1,
v/
v). After centrifugation at 120×
g for 10 min, the supernatant (platelet-rich plasma) was supplemented with EDTA (2 mM) and heparin (6.4 U/mL), incubated for 5 min at 37 °C, and centrifuged at 500×
g for 10 min. The platelet pellet was suspended in 5 mL of Tyrode’s solution, pH 7.3 (containing NaCl (11.9 mM), KCl (2.7 mM), MgCl
2 (2.1 mM), NaH
2PO
4 (0.4 mM), NaHCO
3 (11.9 mM) and glucose (11.1 mM)) and the mixture was incubated for 10 min at 37 °C. After centrifugation of the suspension at 500×
g for 10 min, the washing procedure was repeated. The washed platelets were finally suspended in Tyrode’s solution containing BSA (3.5 mg/mL). The platelet count was monitored by a Coulter counter (Beckman Coulter, Miami, FL, USA). The final concentration of Ca
2+ in the Tyrode’s solution was 1 mM. Washed human platelets (3.6 × 10
8 cells/mL) were incubated with PTE (2–20 μM) or solvent control (0.1% DMSO) for 3 min before stimulation with thrombin (0.01 U/mL) or collagen (1 μg/mL).
4.3. Study of Binding Activated Integrin αIIbβ3
Briefly, washed platelets were preincubated with PTE (3.5 and 6 µM) and FITC-conjugated PAC-1 mAb (2 µg/mL) for 3 min and then stimulated with collagen (1 µg/mL). The suspensions were then assayed for fluorescein-labeled platelets on a flow cytometer (FAC Scan system, Becton Dickinson, San Jose, CA, USA). Data were collected from 50,000 platelets per experimental group, and the platelets were identified based on their characteristic forward and orthogonal light-scattering profiles. All experiments were repeated at least four times to ensure reproducibility.
4.4. Immunoblotting
Washed platelets (1.2 × 109 cells/mL) were preincubated with PTE (3.5 and 6 µM) or 0.1% DMSO for 3 min, and collagen was subsequently added to trigger activation. The platelet suspensions were lysed and separated through 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis. For another study, dishes (6 cm in diameter) were precoated with fibrinogen (100 µg/mL), kept overnight, and then blocked with 1% BSA. Washed platelets (3.6 × 108 cells/mL) were preincubated with PTE (3.5 and 6 µM) or the solvent control (0.1% DMSO) for 3 min and then poured into immobilized fibrinogen dishes for 60 min. The reaction was then stopped, and the platelets were immediately resuspended in 200 μL of lysis buffer. Several proteins were detected using specific primary antibodies. Respective quantitative results were obtained through quantifying the optical density of protein bands by using a video densitometer and Bio-profil BioLight software, version V2000.01 (VilberLourmat, Marne-la-Vallée, France), and relative protein expression was calculated after normalization to the total protein of interest.
4.5. Confocal Microscopy Analysis of Platelet Adhesion and Spreading
Eight-chamber glass tissue-culture slides were coated with either BSA (100 μg/mL) or fibrinogen (100 μg/mL) and left overnight. After washing with phosphate-buffered saline (PBS) twice, the slides were blocked with 1% BSA in PBS for 1 h and then washed again with PBS. Washed platelets (3.0 × 108 cells/mL) preincubated with PTE (3.5 and 6 μM) or the solvent control (0.1% DMSO) were spread on protein-coated surfaces for 45 min. After unbound platelet removal and two washes with PBS, the bound cells were fixed (4% paraformaldehyde), permeabilized (0.1% triton), and stained with FITC-phalloidin (10 μM). All confocal studies were performed using a Leica TCS SP5 microscope equipped with a 63×, 1.40 NA oil immersion objective (Leica, Wetzlar, Germany). The number of platelet adhesion events and the platelet spreading surface area were determined using the NIH ImageJ software (NIH, Bethesda, MD, USA).
4.6. Platelet-Mediated Fibrin Clot Retraction
Washed platelets (3.6 × 10
8 cells/mL) were resuspended in Tyrode’s solution containing 2 mg/mL of fibrinogen and 1 mM CaCl
2 and then dispensed in 500 μL aliquots in glass tubes designed for aggregation [
30]. PTE (3.5 and 6 μM) or the solvent control (0.1% DMSO) was included in the platelet suspension buffer before thrombin (0.01 U/mL)-induced clot retraction without stirring. The reaction was photographed at 15 and 30 min.
4.7. Measurement of Hydroxyl Radicals Through Electron Spin Resonance Spectrometry
The electron spin resonance (ESR) method was used to measure hydroxyl radicals by using a Bruker EMX ESR spectrometer, as described previously [
30]. In brief, platelet suspensions (3.6 × 10
8 cells/mL) were preincubated with PTE (3.5 and 6 μM) for 3 min before adding collagen (1 μg/mL). The reaction was allowed to proceed for 5 min before adding DMPO (100 μM). The ESR spectrometer was operated at a power of 20 mW and 9.78 GHz, and a scan range of 100 G and a receiver gain of 5 ×10
4 were applied [
31]. The ESR signal amplitude was quantified using the WIN-EPR, version 921201 supplied by BRUKER-FRANZEN Analytik GmbH (Bremen, Germany).
4.8. Measurement of Vascular Thrombus Formation in Mouse Mesenteric Microvessels Irradiated with Sodium Fluorescein
The method applied to a thrombogenic animal model in this experiment conformed to the Guide for the Care and Use of Laboratory Animals (8th edition, 2011), and we received an affidavit of approval for the animal use protocol from Taipei Medical University (LAC-2018-0383). Male ICR mice (6 weeks) were anesthetized using a mixture containing 75% air and 3% isoflurane maintained in 25% oxygen; their external jugular veins were then cannulated with a PE-10 tube for administering the dye and drugs intravenously [
28]. Venules (30–40 µm) were irradiated at a wavelength of <520 nm to produce a microthrombus. Two PTE doses (1 and 2 mg/kg) were administered 1 min following sodium fluorescein (15 µg/kg) administration, and the time required for the thrombus to occlude the microvessel (occlusion time) was recorded.
4.9. Statistical Analysis
Continuous variables in the experimental results are presented as the mean ± standard deviation or median (Q1–Q3) depending on whether the data are normally distributed. Values of n refer to the number of experiments; each experiment was conducted using different blood donors. Unpaired Student’s t-test or analysis of variance (ANOVA) was used to determine significant differences among the groups if the data were normally distributed. Mann–Whitney U tests and Kruskal–Wallis tests were conducted for non-normal data. When this analysis indicated significant differences, the groups were compared using the Student–Newman–Keuls method. Statistical significance was set at p < 0.05.