Cardiovascular diseases (CVDs) remain the leading causes of morbidity and mortality globally. The underlying causes of CVDs are complex and multi-factorial involving many risk factors such as abnormal blood lipid, high blood cholesterol levels, overweight and sedentary lifestyle1,2. In particular, platelet dysfunction and aberrant thrombogenesis (thrombus formation) are final underlying pathophysiological processes in the development and progression in CVDs including atherosclerosis, thrombotic complications, stroke and myocardial infarction3. Current anti-platelet agents such as aspirin and clopidogrel are effective at decreasing platelet activation and subsequent risk of atherothrombotic disease, but these agents irreversibly inhibit platelet activation and lead to risks of unwanted hemorrhages4,5. Furthermore, the multi-factorial nature of CVDs urges us to look for versatile pharmacological agents with fewer side effects.

We have reported previously that a novel cardioprotective compound known as ADTM was synthesized in our laboratory by conjugating two well-known active ingredients, DSS and tetramethylpyrazine (TMP), which are present in Chinese medicinal plants, danshen (Salvia miltiorrhizae) and chuanxiong (Ligustium wallichii Franch)6. ADTM displayed strong cardioprotective effects against oxidative stress-induced cellular injury and acute ischemic myocardial infarct in rat, partly through activation of the anti-oxidative stress Nrf2/heme oxygenase-1 (HO-1) pathway7. Several registered pharmaceutical products containing danshen and/or chuanxiong such as “Danshen Dripping Pill” and “Guanxinning Injection” have been widely used in China to treat CVDs. The “Danshen Dripping Pill” was approved by the US Food and Drug Administration (FDA) to undergo Phase III clinical trials in the treatment of CVDs8. Clinical studies indicated that these pharmaceutical products are effective in treating angina pectoris, a symptom of ischemic heart disease9. It is believed that active ingredients in danshen and chuanxiong induce beneficial therapeutic effects by the promotion of better blood circulation10,11. Therefore, we postulated that ADTM might also display anti-platelet and anti-thrombotic properties.

Several members of the protein disulfide isomerases have been shown as important players in the regulation of platelet functions and thrombus formation including PDI, ERp72, ERp57 and ERp512,13,14. However, which member in the family represents the best anti-thrombotic drug target is largely unknown13. The prototypical member PDI is a multifunctional redox chaperone protein that plays critical roles in a variety of diseases including platelet aggregation and thrombus formation in vivo and in vitro15,16,17. More recently, it is shown that blood platelets also secreted ERp57 (also known as GRP58 and PDIA3) in response to vascular injury to trigger platelet activation and aggregation and emerges as a novel target for anti-platelet aggregation and anti-thrombosis18,19,20. Human ERp57 has 32% amino acid sequence homology with PDI and exhibits 40% identity with the a-b-b´-a´domains of ERp7221. However, selective chemical agents for ERp57 are not yet available.

In this study, we further identified the drug target of ADTM as ERp57 by using a chemical proteomics approach analyzing liquid chromatography linked to tandem mass spectrometry (LC-MS/MS) profile of pull-down proteins bound to a biotinylated-ADTM analogue (BAA). The anti-platelet aggregation and anti-thrombosis activities of ADTM were determined both in vitro and in vivo. The results provided promising evidences for the potential of developing novel anti-CVD and anti-thrombotic agents with selectivity at the protein disulfide isomerases by using ADTM.


Protein disulfide isomerases are identified as targets of ADTM by chemical proteomics

In order to isolate the protein targets that bound to ADTM, a biotin-conjugated ADTM analogue (BAA, Fig. 1) was designed and synthesized in our laboratory as described in Supplementary Methods (Supplemental Fig. 3). BAA (300 μM) was incubated with rat blood platelet lysates and the BAA-protein complexes were pulled down with NeutrAvidin-agarose followed by protein profiling using LC-MS/MS. It was observed that BAA could bind to various proteins involved in platelet function, including glycoprotein 5 (a potential marker of thrombotic platelet activation22,23), superoxide dismutase and xanthine oxidase (regulators of vascular redox signaling24). In particular, four platelet aggregation-associated proteins were identified with >95% protein identification probability (Supplementary Table S1), including ERp72, ERp57 ERp5 and PDI, which are glycoprotein-specific members of the PDI family related to platelet function and redox homeostasis25,26. We confirmed the identity of the pulled-down proteins as ERp72, ERp57 and ERp5 with their respective antibodies by using immunoblot analysis (Fig. 2b). Furthermore, the specificity of the binding between BAA and these targets (ERp72, ERp57 and ERp5) could be demonstrated by the competition with untagged ADTM in excess (Fig. 2a). The molecular docking analysis demonstrated that the free binding energy to the active cavity of ERp57 (PDB: 3F8U) is −6.5 kcal/mol. ADTM may form hydrogen bonds with side chains of ARG47, ILE453 and PHE450, respectively, in the catalytic center (CYS406/CYS409) of ERp57 (Supplemental Fig. 2). ERp72, ERp57, ERp5 and PDI are identified as important new targets in redox homeostasis of blood platelet aggregation12, therefore we further evaluated the effects of ADTM on the reducing activities of the PDI family members. As shown in Fig. 2c, ADTM exhibited potent inhibition on the redox activity of ERp57 in a concentration-dependent manner (IC50 = 100 to 300 μM). ADTM inhibited the activities of ERp72, ERp5 and PDI to a much lesser extent (18%, 38% and 30% of inhibition at 300 μM, respectively), displaying differential inhibitory activity at ERp57 (order of potency as follows: ERp57 > ERp5 > PDI > ERp72). ERp57 inhibition by ADTM was irreversible after dilution of the ERp57-ADTM complex (Supplemental Figure 1), indicating that ADTM may covalently bind ERp57.

Figure 1
figure 1

Chemical structures of DSS, TMP, ADTM and BAA.

Figure 2
figure 2

Target validation and the inhibition of PDI members by ADTM.

(a) Schematics of the target validation. (b) Proteins isolated from rat platelets were pretreated with DMSO or excess amount of untagged ADTM for 2 h, followed by treatment with BAA for another 2 h and compound-protein-complexes were enriched with NeutrAvidin-agarose resin. The precipitates were detected by immunoblot for indicated proteins of PDI family. (c) ADTM selectively inhibits ERp57. The recombinant PDI, ERp57 and ERp72 proteins were incubated with different concentrations of ADTM for 100 min and its catalytic activity was determined in insulin reduction assay.

ADTM inhibits platelet aggregation in vitro

It was observed that ADTM exhibited concentration-dependent inhibition on ADP-induced platelet aggregation (Fig. 3a) as well as AA-induced platelet aggregation (Fig. 3b) in vitro and its effects were comparable to first-line clinical anti-platelet drugs, aspirin and clopidogrel. The parent compounds DSS and TMP, alone or in combination, could only inhibit AA-induced platelet aggregation but not ADP-induced platelet aggregation. These results demonstrated that ADTM exhibited broad-spectrum anti-platelet activities.

Figure 3
figure 3

Inhibitory effects of ADTM on ADP-and AA-induced platelet aggregation in vitro.

Platelets were pretreated with or without the indicated concentrations of the tested compounds, ADTM (1–100 μM), DSS (100 μM), TMP (100 μM), aspirin (1–100 μM) and clopidogrel (1–100 μM) for 5 min at 37 °C and the percentage (%) of platelet aggregation inhibition normalized to DMSO treated samples (vehicle control) was determined as described in Materials and Methods. The platelets were stimulated with ADP (a) and AA (b). Data are expressed as mean ± SD, *P < 0.01 compared with the 100 μM DSS group. #P < 0.01 compared with the 100 μM TMP group, &P < 0.01 compared with the 100 μM DSS + TMP group, n ≥ 3/group. D = DSS, T = TMP, ASA = aspirin, clop = clopidogrel.

ADTM inhibits the expression of P-selectin

To further investigate the underlying mechanism of ADTM anti-platelet activity, we examined the effect of ADTM on the expression of P-selectin (also known as CD62P), which is an adhesion molecule expressed on the surface of platelet and is a critical marker of platelet activation, by using immunoreactivity and flow cytometry analysis. We observed that ADTM concentration-dependently inhibited ADP-induced expression of P-selectin and attenuated the expression of P-selectin by more than 65% at 100 μM (Fig. 4a and 4b).

Figure 4
figure 4

ADTM inhibited the expression of P-selectin.

Whole blood was treated with DMSO (0.1%) as a control or the indicated concentrations of ADTM (1–100 μM) for 5 min at 37 °C. After that the platelets were activated using ADP (10 μM). Flow cytometry histogram (a) and the quantification of the data (b) show that ADTM inhibits P-selectin binding to ADP-activated platelets. #P < 0.01 compared with the control group, *P < 0.01 compared with the ADP group. Data are representative of three independent experiments.

ADTM inhibits activation of αIIbβ3 and disrupted ERp57/αIIbβ3 interaction

Recently, ERp57 has been reported to directly interact with αIIbβ3 integrin and regulate its function in platelet aggregation20. In line with this, we observed that ADTM could modulate αIIbβ3 and concentration-dependently inhibited ADP-induced αIIbβ3 activation, by using flow cytometry analysis with PAC-1, a monoclonal antibody that binds only the activated form of αIIbβ3 (Fig. 5a,b). We further examined the action of ADTM on the ERp57/αIIbβ3 interaction by immunoprecipitation with anti-αIIbβ3 antibody, followed by detection of ERp57 immunoreactivity using immunoblotting. It was found that ADTM disrupted the interaction of ERp57 with αIIbβ3, both in the presence and absence of ADP (Fig. 5c).

Figure 5
figure 5

ADTM inhibits activation of αIIbβ3 integrin and disrupts the ERp57/αIIbβ3 complex on platelets.

Representative flow cytometry histogram (a) and the quantification of the data (b) show that ADTM inhibits PAC-1 binding to ADP-activated platelets. (c) ADTM disrupts the ERp57/αIIbβ3 complex. Whole blood was treated with DMSO (0.1%) as a control or 100 μM ADTM for 5 min at 37 °C. After that the platelets were activated using ADP (10 μM). Platelet lysates were prepared for immunoprecipitation (IP) and probed with anti-ERp57 antibody for immunoblot analysis (IB). The precipitates were also blotted with anti-αIIbβ3 antibody to ensure that equal amounts of αIIbβ3 were pulled down under each condition. #P < 0.01 compared with the control group, *P < 0.01 compared with the ADP group. Data are representative of three independent experiments.

ADTM increases vasodilator-stimulated phosphoprotein (VASP) phosphorylation and HO-1 protein level

In platelets, the phosphorylation of VASP is involved in the down-regulation of platelet aggregation accompanied by inhibition of platelet integrin αIIbβ3 activation27,28. As shown in Fig. 6a, pretreatment with ADTM (10 and 100 μM) stimulated approximately three-fold increase in the phosphorylation of VASP. In addition, we also observed that ADTM increased the protein expression of HO-1, an anti-oxidative stress microsomal enzyme which when up-regulated could inhibit platelet-dependent thrombus formation (Fig. 6b)29.

Figure 6
figure 6

Effects of ADTM on VASP phosphorylation and HO-1 protein Level.

Rat platelets (1 × 108 platelets/ml) were incubated with DMSO and various concentrations of ADTM for 10 min followed by treatment with ADP for 5 min. Proteins were extracted from the rat platelets and then analyzed by immunoblot using antibodies against VASP and HO-1 as described in Materials and Methods. ADTM increased VASP phosphorylation (a) and HO-1 protein expression (b). *P < 0.05 compared with the ADP-stimulated group.

Inhibition of platelet aggregation and thrombus formation by ADTM in vivo

Various concentrations of ADTM were administered in rats in vivo (10 –20 mg/kg, 5 days, intravenous, IV) and the platelet aggregation activity and the thrombus formation were evaluated. As shown in Fig. 7, ADP-induced platelet aggregation was significantly compromised (>40% reduction) in rats treated with ADTM (20 mg/kg). Similarly, ADTM also exhibited significant anti-thrombotic effect in vivo as shown in the ferric chloride (FeCl3)-induced venous thrombosis (Fig. 8a). The inhibitory effects of ADTM in platelet aggregation and thrombus formation were comparable to clopidogrel. Furthermore, FeCl3 induced significant decrease in plasma 6-Keto-PGF (an indicator of plasma PGI2, an intrinsic inhibitor of platelet aggregation) and the treatment of ADTM (20 mg/kg, 5 days, IV) abolished the reduction of FeCl3-induced 6-Keto-PGF in a concentration-dependent manner (Fig. 8b), giving more evidence of the anti-thrombotic properties of ADTM.

Figure 7
figure 7

ADTM inhibits platelet aggregation-induced by ADP in a concentration-dependent manner in vivo.

In order to compare the activities of ADTM, DSS, TMP, DSS + TMP and clopidogrel at a similar blood concentration, 20 mg/kg of ADTM (MW: 444), 10 mg/kg of DSS (MW: 220) and 6 mg/kg of TMP (MW: 136) alone and in combination and 18 mg/kg of clopidogrel (MW: 322) were administered by IV injection once daily. This resulted in approximately the same blood concentration of ADTM, DSS, TMP, DSS + TMP and clopidogrel in rats in vivo. Five days after drug treatment, blood was withdrawn and ADP-induced platelet aggregation was measured. Data are expressed as mean ± SD, n ≥ 6/group. D = DSS, T = TMP, clop = clopidogrel, MW = molecular weight.

Figure 8
figure 8

Anti-thrombotic effect of ADTM in the FeCl3-induced rat thrombosis model.

The anti-thrombotic effect of ADTM in the FeCl3-induced inferior vena cava thrombosis model (a). In order to compare the activities of ADTM, DSS, TMP and clopidogrel at similar blood concentrations, the compounds were administered by IV injection as described in Fig. 7. The effect of ADTM on plasma 6-Keto-PGF1a concentration in the FeCl3-induced thrombosis model (b). Data are expressed as mean ± SD, #P < 0.01 compared with the sham group, *P < 0.05 compared with the vehicle group, n = 5–7/group, D = DSS, T = TMP, clop = clopidogrel.


Anti-thrombotic therapy plays an essential role in the course of treatment of various cardiovascular disorders (CVDs) because platelet dysfunction and thrombogenesis are common underlying factors in the development and progression in CVDs, particularly atherosclerosis, myocardial infarction and ischemic stroke. Aspirin and clopidogrel are most routinely used anti-platelet agents for the management of CVDs, but these agents irreversibly inhibit platelet activation with potentially devastating unwanted effects such as hemorrhages. In present study we reported that ADTM, a novel cardioprotective compound synthesized in our own laboratory6, displayed specific binding for several members of the PDI family. By using a biotin-conjugated ADTM analogue (BAA) as bait and chemical proteomic analysis of the bound protein complexes, we identified eight potential interacting protein targets of ADTM (Supplementary Table S1). With further validation using immunoblot analysis the identity of major targets were confirmed as members of the PDI family, including ERp72, ERp57 and ERp5. In particular, ADTM showed highest potency in inhibiting the redox activity of ERp57 in enzymatic assay in vitro. Furthermore, untagged-ADTM could compete with BAA for the binding of ERp57, providing evidence that ADTM is a competitive ligand at ERp57. We further demonstrated that ADTM displayed concentration-dependent inhibition in ADP-induced platelet aggregation and AA-induced platelet aggregation in vitro. This result is in line with the observation that ERp57 has been recently implicated to play crucial roles in mediating platelet aggregation, homeostasis and thrombosis18,19,20. It has also been reported that ERp57 present on platelet surface were activated by staphylococcal extracellular adhesive protein resulting in arteriosclerosis in Staphylococcus aureus infection and the inhibition of ERp57 could suppressed platelet aggregation30.

We further demonstrated that ADTM concentration-dependently inhibited the ADP-induced expression of P-selectin and activation of αIIbβ3 integrin in vitro. P-selectin is an adhesion molecule expressed on the surface of platelet and is an important marker for platelet activation. αIIbβ3 integrin is the most abundant adhesion receptor on the surface of circulating platelets and has been reported to mediate platelet aggregation through strong interactions with adhesive proteins such as fibrinogen, von Willebrand factor and fibronectin31. We further demonstrated that ERp57 bound to αIIbβ3 directly by using co-immunoprecipitation and ADTM disrupted ERp57/αIIbβ3 interaction, as shown by the dissociation of the complex (Fig. 5c). In line with this, ERp57 has been reported to directly interact with αIIbβ3 on platelet surface and regulate its function in platelet aggregation18,19,20. Recent study has shown that disulfide bond exchanges in αIIbβ3 is required for activation and post-ligation signaling during clot retraction32 and the modulation of functional disulfide bonds is being explored for blood protein control33. Our results suggested that ADTM produced its anti-thrombotic action via the modulation of disulfide bond by interacting with ERp57 (Fig. 9).

Figure 9
figure 9

Proposed mechanism of ADTM anti-platelet aggregation.

In part, ADTM binds with ERp57 and inhibits its redox activity, inhibits the activation of αIIbβ3 and the expression of P-selection and enhances the expression of HO-1 and phosphorylation of VASP. The crosstalk between ERp57 and αIIbβ3 is involved in the biological action of ADTM. In addition, ADTM reverses the decreased level of 6-Keto-PGF1α, a stable metabolite of PGI2 in the FeCl3-induced thrombosis model in vivo.

The inhibitory action of ADTM on platelet integrin αIIbβ3 activation was furthered evidenced by the increase of the phosphorylation of VASP after ADTM pretreatment. The phosphorylation VASP is involved in the down-regulation of platelet aggregation accompanied by inhibition of platelet integrin αIIbβ3 activation27,28. We also observed that ADTM increased the expression of HO-1 in platelets. This is coherent with our previous finding that HO-1 activation has a key role in ADTM cardioprotective effect in H9c2 cardiomyoblast cells in vitro and in the myocardium in vivo7. HO-1 is a potential therapeutic target in treating thrombotic disease and HO-1 knockout mice demonstrated acute thrombus formation in response to hypoxia34. Previous studies reported that dengue virus glycoprotein-1 (DV-NS1) antibody inhibited PDI activity and blocked platelet aggregation accompanied by an increase in HO-135,36. Furthermore, redox reactions have been shown to play crucial roles in platelet aggregation in a glutathione peroxidase-3 (GPx-3)-deficient mouse model. GPx-3 is an important anti-oxidant enzyme and redox sensor in plasma and GPx-3-deficiency impaired normal platelet inhibition and promoted thrombosis due to enhanced reactive oxygen species flux and decreased nitric oxide bioavailability37. In our in vivo studies, we observed that ADP-induced platelet aggregation was significantly compromised (>40% reduction) in rats treated with ADTM (20 mg/kg). The anti-thrombotic effect of ADTM was further evidenced by the reduction of platelet activity and thrombus formation in the ferric chloride (FeCl3)-induced venous thrombosis assay in the rat. The major metabolites of ADTM in vivo were 2-hydroxymethy-3, 5, 6-trimethylpyrazin (TMP-OH) and DSS38. We have checked the in vivo activity of DSS and TMP. Interestingly, the results showed that ADTM exhibited stronger antiplatelet and anti-thrombotic activities when compared to DSS and TMP, alone or in combination in ADP-induced platelet aggregation and FeCl3-ionduced thrombosis model, respectively (Figs. 7 and 8). The precise mechanisms of this action conferred by ADTM would be another interesting question that is worth investigating in the future. Recently there are accumulating reports that the inhibition of protein disulfide isomerases including PDI and ERp57 could block thrombus formation in various in vivo models and suggest that this protein family represents an important novel class of anti-thrombotic target39,40,41,42,43. Preclinical studies demonstrate that deficiency in platelet ERp57 resulted in the increased tail bleeding times and delayed thrombus formation20, while PDI is unable to compensate for the absence of platelet ERp5720 and other study also showed that the blockade of ERp57 with specific antibody further inhibited platelet aggregation in PDI deficient platelets16. These independent studies further provided evidences that ERp57 and PDI have distinct roles in the mediation of platelet function.

Taken together, our present study reported the anti-thrombotic action of ADTM with both in vitro and in vivo data. ADTM exhibited comparable anti-thrombotic properties as aspirin and clopidogrel. The results suggested that the anti-thrombotic action of ADTM is mediated through disrupting the interaction between ERp57 and αIIbβ3 possibly by blocking the action of ERp57 on disulfide bonding (Fig. 9). Our data provided a rationale for the further development of ADTM as anti-thrombotic agent targeting the underlying mechanism involving ERp57 and αIIbβ3. Furthermore, as a competitive ligand at ERp57, ADTM presents as a promising compound for the development of versatile anti-thrombotic agents. Our data also provide insights in novel strategies for the development of drugs targeted ERp57 for anti-thrombotic.



ADTM and BAA were synthesized at Jinan University, China. DSS and TMP were of analytical pure grade and obtained from Xi’an Honson Biotechnology (China) and Shanghai Banghai Chemical Company (China), respectively. Human recombinant ERp57 was obtained from Abcam (Cambridge, UK), PDI and ERp72 were purchased from Enzo Life Sciences (Exeter, UK). Insulin, DTT, AA and ADP were obtained from Sigma Aldrich (St. Louis, MO, USA).

Preparation of platelet-rich plasma

All animal experiments were approved by the Animal Care and Experimentation Committee of Jinan University and were performed in accordance with the approved guidelines. Sprague-Dawley rats were anesthetized with 10% chloral hydrate and blood was obtained by an arterial puncture. Whole blood was anticoagulated with citrate (3.8%; 1:9, v/v) and centrifuged at 200 g for 8 min at room temperature to obtain platelet-rich plasma (PRP). The residue was centrifuged at 550 g for 5 min to obtain platelet-poor plasma (PPP).

Protein preparation from platelets

Washed platelets were lysed using a dounce homogenizer in NP-40 lysis buffer (Beyotine, China) with 1 mM phenylmethylsulfonyl fluoride (PMSF). Platelet lysates were centrifuged at 12,500 g for 20 min at 4 °C and the supernatant was collected and stored at −80 °C until further analysis.

NeutrAvidin Agarose Resin pull-down with BAA

Platelet lysates (3 μg/μl) were exposed to NeutrAvidin Agarose Resin (Pierce Biotech., Rockford, IL, USA) for 2 h at 4 °C and then centrifuged for 3 min at 2,500 g. The resin was discarded to remove endogenous biotin. Aliquots of supernatants (300 μl) were first treated with DMSO or ADTM (600 μM) for 2 h and then incubated with BAA (600 μM) for another 2 h. The supernatant was combined with NeutrAvidin Agarose Resin and allowed to shake overnight at 4 °C as described previously44. To eliminate the nonspecific combination with compound or agarose resin before protein analysis, 0.1% DMSO was added to one aliquot of lysate as a negative control.

Nano LC-MS/MS analysis

The compound-protein complex bound to agarose resin was digested with trypsin. The digested peptides were analyzed with 1D nano-RP LC-MS/MS. Acquired MS data were analyzed using the Paragon algorithm in ProteinPilot 4.0 software (Applied Biosystems, Framingham, MA, USA). The identified peptides from the Paragon algorithm were grouped into minimal non-redundant protein sets by the ProGroup algorithm of the software (details of this method can be found in Supplementary Methods).

Immunoblot analysis

Proteins eluted from the resin were subjected to SDS-PAGE and then transferred to a PVDF membrane for immunoblot (details in Supplementary Methods).

Insulin reduction assay

PDI activity was measured using an assay that measured the catalytic reduction of insulin, as described previously with minor modifications39,45. Briefly, insulin (1 mg/ml) was freshly prepared in assay buffer (100 mM potassium phosphate, 1 mM EDTA (pH 7.4) and 10 μM dithiothreitol). 50 μl of insulin was incubated in the presence of 10 μl of enzyme and varying concentrations of compound and then 10 μl of 0.1 mM dithiothreitol was added. The increase in turbidity was monitored at 620 nm using a microplate reader (Perkin-Elmer, Singapore) at 25 °C for 60 min. PDI, ERp57 and ERp72 were all used at 0.04 mg/ml. PDI family enzyme inhibition in the presence of compound was determined by the following formula: enzyme inhibition (%) = [1–(OD[compound + PDI + DTT]–OD[DTT])/(OD[PDI + DTT]–OD[DTT])] × 100%.

Platelet aggregation in vitro

The inhibitory effect of ADTM was examined as previously described with modifications39. Briefly, platelets were incubated with the indicated concentrations of compounds or 0.1% DMSO at 37 °C for 5 min with shaking. Aggregation was induced by ADP (10 μM) or AA (200 μM) and measured using a platelet aggregometer (SC-2000, Saikexide Instrument Co. Ltd. China). Inhibition of aggregation was calculated using the following general formula: inhibition of aggregation = (rate of aggregation in vehicle group – rate of aggregation in treated group)/rate of platelet aggregation in vehicle group × 100%.

Determination of human platelet activation by flow cytometry

Flow cytometry and immunoprecipitation studies involving human platelets were approved by Jinan University with informed consent in accordance with the World Medical Association Declaration of Helsinki and carried out in accordance with the approved guidelines. Flow cytometry was performed as described in the Supplementary Methods. PE conjugated anti-CD62P (P-selectin) antibody and FITC conjugated anti-PAC-1 (activated αIIbβ3) antibody were used to detect platelet activation markers after exposure to ADP in the presence of DMSO (0.1%) or different concentrations of ADTM. An isotype-matched IgG1 PE/FITC was used as a negative control.


To determine ERp57-bound αIIbβ3 contents, whole platelet lysates were incubated with anti-αIIbβ3 antibody overnight at 4 °C under agitation. The antigen-antibody complex was pulled down after incubation for 4 h at 4 °C with protein G-agarose (Cell Signaling Technology) as described previously46. Immune complexes were boiled for 5 min with 2 × loading buffer followed by immunoblot analysis with antibodies for ERp57 and αIIbβ3.

Rat platelet aggregation-induced by ADP in vivo

To study the effects of ADTM on platelet aggregation in vivo, ADTM (5–20 mg/kg) in comparison with DSS (10 mg/kg), TMP (6 mg/kg), DSS (10 mg/kg) + TMP (6 mg/kg) and clopidogrel (18 mg/kg) were administered daily by IV injection for 5 days, respectively (detailed methodology in Supplementary Methods). Platelet aggregation was monitored for 5 min and the maximum aggregation inhibition (%) was calculated.

FeCl3-induced inferior vena cava thrombosis in rat

Rats weighing 180 g to 220 g were anesthetized by intraperitoneal administration of 10% chloral hydrate. One hour post-treatment, the medioventral line in the rats was cut and the inferior vena cava was surgically exposed by blunt dissection. 1 × 1 cm filter paper, soaked in 50% FeCl3 solution, was placed under and above the exposed inferior vena cava for 15 min. Subsequently, the thrombosed inferior vena cava was carefully dissected and the weight (mg) of wet thrombus harvested from the inferior vena cava was measured as described previously47.

Evaluation of plasma 6-Keto-PGF levels in rat

The concentration of 6-keto-PGF present in the supernatant was measured using a radioimmunoassay kit (New England Nuclear Dupont, Boston, MA) according to the manufacturer’s instructions. Blood was collected into plastic tubes containing 10% EDTA-Na2. Plasma was prepared by centrifuging blood at 550 g for 10 min. Plasma concentrations of 6-keto-PGF were determined by radioimmunoassay and expressed as pg/ml.

Statistical analysis

All assays were performed at least three times. Data are presented as mean ± SD. The groups were compared using one-way ANOVA followed by Tukey’s multiple comparison tests using the statistics module of Graph Pad Prism 5.0. A value of P < 0.05 was considered statistically significant.

Additional Information

How to cite this article: Cui, G. et al. Novel anti-thrombotic agent for modulation of protein disulfide isomerase family member ERp57 for prophylactic therapy. Sci. Rep. 5, 10353; doi: 10.1038/srep10353 (2015).