Printer Friendly

Low-level mercury can enhance procoagulant activity of erythrocytes: a new contributing factor for mercury-related thrombotic disease.

BACKGROUND: Associations between cardiovascular diseases and mercury have been frequently described, but underlying mechanisms are poorly understood.

OBJECTIVES: We investigate the procoagulant activation of erythrocytes, an important contributor to thrombosis, by low-level mercury to explore the roles of erythrocytes in mercury-related cardiovascular diseases.

METHODS: We used freshly isolated human erythrocytes and ex vivo and in vivo thrombosis models in rats to investigate mercury-induced procoagulant activity.

RESULTS: Prolonged exposure to low-dose mercuric ion ([Hg.sup.2+]; 0.25-5 [micro]M for 1-48 hr) induced erythrocyte shape changes from discocytes to echinocytes to spherocytes, accompanied by microvesicle (MV) generation. These MVs and remnant erythrocytes expressed phosphatidylserine (PS), an important mediator of procoagulant activation. [Hg.sup.2+] inhibited flippase, an enzyme that recovers PS into the inner leaflet of the cell membrane, and activated scramblase, an enzyme that alters lipid asymmetry in the cell membrane. Consistent with these activity changes, [Hg.sup.2+] increased intracellular calcium and depleted ATP and protein thiol. A thiol supplement reversed [Hg.sup.2+]-induced MV generation and PS exposure and inhibited the increase in calcium ion ([Ca.sup.2+]) and depletion of ATP, indicating that free-thiol depletion was critical to [Hg.sup.2+]-mediated procoagulant activity. The procoagulant activity of [Hg.sup.2+]-treated erythrocytes was demonstrated by increased thrombin generation and endothelial cell adhesion. We further confirmed [Hg.sup.2+]-mediated procoagulant activation of erythrocytes in ex vivo and in vivo rat thrombosis models, where [Hg.sup.2+] treatment (0.5-2.5 mg/kg) increased PS exposure and thrombus formation significantly.

CONCLUSION: This study demonstrated that mercury could provoke procoagulant activity in erythrocytes through protein-thiol depletion--mediated PS exposure and MV generation, ultimately leading to enhanced thrombosis.

KEY WORDS: erythrocyte, mercury, phosphatidylserine exposure, procoagulant activity. Environ Health Perspect 118:928-935 (2010). doi:10.1289/ehp.0901473 [Online 23 March 2010]

Mercury (Hg) is a heavy metal element widely distributed in the earth's crust, seawater, freshwater, and air (Environment Canada 2004). Concomitantly with modern industrialization, human exposure to mercury has increased through anthropogenic mercury emissions from fuel combustion, municipal incinerators, and chemical industries. Mercury is considered a major environmental toxicant throughout the world (Agency for Toxic Substances and Disease Registry 2007; Mahaffey and Mergler 1998; Salonen et al. 2000; Valera et al. 2008), and much effort is being directed toward reducing environmental mercury pollution (Trasande et al. 2005). In a study of New York City adults, the mean blood mercury level was 2.73 [micro]g/L, higher than blood lead or cadmium levels (McKelvey et al. 2007). Moreover, in that study, consumers of high-fish diets exhibited 3.7 times the blood mercury levels observed in those who reported consuming no fish. In another study, Akagi et al. (1995) reported that some people living in areas active in gold mining showed an extremely high level of blood mercury, close to 150 [micro]g/L (~ 0.75 [micro]M), raising a strong concern over the mercury exposure problem.

Mercury is harmless in insoluble form, but vapor or soluble forms such as inorganic mercury or methylmercury can be extremely toxic to humans. Most human mercury exposure occurs through inhalation of elemental mercury vapor released from dental amalgam and through the consumption of fish contaminated with methylmercury (Berlin et al. 2007). Once inhaled, elemental mercury vapor is rapidly accumulated into erythrocytes and undergoes oxidation to the mercuric ion ([Hg.sup.2+]) by catalase. Orally absorbed methylmercury is preferentially distributed into erythrocytes (~ 90%) and slowly turns into [Hg.sup.2+] through demethylation in the spleen and liver. It has been demonstrated that 6-15% of total mercury in the blood of populations consuming high-fish diets exists in the form of inorganic mercury (Berglund et al. 2005; Rodrigues et al. 2010). Because elemental mercury or methylmercury ultimately turns into [Hg.sup.2+] in the body (Zalups 2000), mercuric salt has been commonly used to investigate the toxicity of mercury.

Mercury toxicity mainfests mainly as neuronal disorders, immunotoxicity, and kidney damage (Clarkson et al. 2003); however, cardiovascular diseases (CVDs), including atherosclerosis, coronary heart diseases, pulmonary embolism, hypertension, and vessel obstruction, have been frequently described in relation to mercury exposure (Houston 2007; Virtanen et al. 2005, 2007). Previously, CVDs associated with mercury exposure have been assumed to occur as a consequence of renal effects of mercury, but increasing attention is also being given to direct effects of mercury on cardiovascular (CV) tissues, including blood vessels, endothelial cells (Wiggers et al. 2008), platelets (Macfarlane 1981), and erythrocytes (Suwalsky et al. 2000). However, the role of direct toxic effects of mercury on CV tissues in the pathogenesis of mercury-associated CVDs has not been clarified.

Well-characterized hemolytic and anemia-inducing effects of mercury suggest that the erythrocyte might be an important target of mercury (Zolla et al. 1997). Eisele et al. (2006) reported that low-level [Hg.sup.2+] exposure can induce phosphatidylserine (PS) translocation to the external surface of the erythrocyte cell membrane (i.e., PS exposure) through the modulation of a clotrimazole-sensitive potassium ion ([K.sup.+]) channel. These authors described the PS-exposing effects of [Hg.sup.2+] in relation to the apoptosis of etythrocytes. However, the implications of PS-externalized erythrocytes in procoagulant activation and subsequent CVDs were not addressed. In another study, alterations of the erythrocyte membrane, including PS exposure and PS-bearing microvesicle (MV) formation,

were reported to be able to render erythrocytes procoagulant, enabling the active participation of erythrocytes in thrombosis (Chung et al. 2007). PS exposed on the surface of erythrocytes provides a site for the assembly of the prothrombinase and tenase complex, leading to efficient thrombin generation and ultimately to clotting (Zwaal et al. 1977; Zwaal and Schroit 1997). Furthermore, increased adhesion of PS-expressing erythrocytes to endothelial cells contributes to vasoocclusion (Closse et al. 1999). MVs generated from deformed erythrocytes through vesiculation also contribute to an acceleration of the coagulation cascade via strong procoagulant activity and by serving as a rich source of PS (Martinez et al. 2005).

In the present study, we discovered that both MV generation and PS exposure could be induced in human erythrocytes by low-dose ([Hg.sup.2+]) (Hg[Cl.sub.2], 0.25-5[micro]M). Of note, [Hg.sup.2+]-mediated PS exposure and MV generation could enhance thrombin generation and adhesion to vascular endothelial cells, which is considered a direct marker for procoagulant activity. We examined the mechanism underlying, and in vivo relevancy of, [Hg.sup.2+]-induced procoagulant activation of erythrocytes in an effort to gain insight into the CVDs associated with mercury exposure.

Materials and Methods

Materials. We purchased mercury chloride (Hg[Cl.sub.2]), calcium chloride (Ca[Cl.sub.2]), EDTA, bovine serum albumin (BSA), [KH.sub.2][PO.sub.4], NaCl, [Na.sub.2][HPO.sub.4], KCl, Tris/HCl, Mg[Cl.sub.2], Na[H.sub.2][PO.sub.4], dextrose, sodium citrate, Tris-base, NaHC[O.sub.3], dimethyl sulfoxide, ethanol, Triton X-100, trichloroacetic acid, Tris-acetate, ATP bioluminescent assay kit, iodoacetic acid, adenosine, ethylene glycol tetraacetic acid (EGTA), acetic acid, purified human thrombin, and calcium ionophore A23187 from Sigma Chemical Co. (St. Louis, MO, USA). Other chemicals were of the highest grade available.

Preparation of human erythrocytes. This study was approved by the Institutional Review Board at the Seoul National University/Health Service Center, and all subjects provided written informed consent. On the day of each experiment, human blood was obtained from healthy male donors (18-25 years of age) into Vacutainers containing acid citrate dextrose (Becton Dickinson, San Diego, CA, USA). Platelet-rich plasma and buffy coat were removed by aspiration after centrifugation at 200 x g for 15 min. Packed erythrocytes were washed three times with phosphate-buffered saline (PBS; 1 mM [KH.sub.2][PO.sub.4], 154mM NaCl, 3 mM [Na.sub.2][HPO.sub.4],pH7.4) and once with Tris buffer (15 mM Tris-HCl, 150 mM NaCl, 5 mM KCl, 2 mM Mg[Cl.sub.2],pH 7.4) or Ringer solution (125 mM NaCl, 5 mM KCl, 1 mM MgS[O.sub.4], 32 mM HEPES, 5 mM glucose, pH 7.4). Washed erythrocytes were resuspended in Tris buffer or Ringer solution to a cell concentration of 5 x [10.sup.7] cells/mL, and the final Ca[Cl.sub.2] concentration was adjusted to 1 mM before use.

Microscopic observation using scanning electron microscopy and confocal microscopy. After fixation with 2% glutaraldehyde solution for 1 hr at 4[degrees]C, the erythrocytes were centrifuged and washed three times with PBS, followed by postfixation with 1% osmium tetroxide for 30 min at room temperature. After washing with PBS several times, the samples were dehydrated serially with 50%, 75%, 90%, and 100% ethanol. After drying and coating with gold, the images were observed on a scanning electron microscope (SEM; JEOL, Tokyo, Japan). For confocal microscopy, 200 [micro]L erythrocyte suspension was added and attached for 1 hr to an eight-chambered coverslip (Lab-Tek; Nalge Nunc Inc., Naperville, IL) that had been coated with 0.1 mg/mL poly-L-lysine. After washing the coverslip three times with Tris-buffered saline (TBS) containing 2% BSA, erythrocytes were stained with TBS buffer containing anti--glycophorin-A--FITC for 30 min and washed three times again. Erythrocytes were then incubated with vehicle (TBS) or [Hg.sup.2+] and observed using confocal microscopy equipped with an argon laser (Leica, Wetzlar, Germany). Excitation and emission filters were set at 488 nm and 550-600 nm, respectively.

Flow cytometric analysis of PS exposure and cytosolic calcium in erythrocytes. We used fluorescein isothiocyanate (FITC)-labeled annexin V (annexin V-FITC; Pharmingen, San Diego, CA, USA) as a marker for PS positivity and phycoerythrin-labeled monoclonal antibody against human glycophorin A (anti-glycophorin A--RPE; Dako Cytomation, Glostrub, Denmark) to identify erythrocytes. Negative controls for annexin V binding were stained with annexin V-FITC in the presence of 2.5 mM EDTA instead of 2.5 mM Cs[Cl.sub.2]. For detection of intracellular calcium increase, erythrocytes were loaded with 3 [micro]M Fluo-4-AM (Molecular Probes, Eugene, OR, USA) for 1 hr at 37[degrees]C in the dark. Subsequently, the cells were washed twice and then resuspended in Tris buffer to a final concentration of 5 x [10.sup.7] cells/mL with 1 mM of Ca[Cl.sub.2]. For the confirmation of interference of Fluo-4 calcium signal by [Hg.sup.2+], N, N, N, N-tetrakis(2-pyridylmethyl) ethylenediamine (TPEN; 100 [micro]M; Sigma Chemical Co.) was added for 5 min to extract Fluo-4-bound [Hg.sup.2+]. To quench extracellular calcium, 3 mM EGTA was added to the erythrocyte suspension. Samples were analyzed on a FACScalibur flow cytometer (Becton Dickinson). Data from 10,000 events were collected and analyzed using CellQuest Pro software (Becton Dickinson).

Phospholipid translocation measurement. We measured phospholipid translocation according to the method described by Hilarius et al. (2004). Briefly, erythrocytes (5 x [10.sup.7] cells/mL) were incubated with [Hg.sup.2+] and then loaded with 0.5 [micro]M 1-Palmitoyl-2-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl) amino] hexanoyl]-sn-glycero-3-phospho-L-serine ([C.sub.6]-NBD-PS; Avanti Polar Lipids, Alabaster, AL, USA) for the flippase activity assay or 1-oleoyl-2-[6-[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino]hexanoyl]-sn-glycero-3-phosphocholine ([C.sub.6]-NBD-PC; Avanti Polar Lipids) for the scramblase activity assay. Aliquots of cell suspension were removed at the indicated time intervals, placed in cold Tris buffer, and incubated on ice for 10 min in the presence or absence of 1% BSA. The amount of internalized probe was determined by comparing the fluorescence intensity associated with the cells before and after back-extraction by BSA. Samples were analyzed on the FACScalibur flow cytometer.

Intracellular ATP level measurement. After incubation with [Hg.sup.2+], erythrocytes were washed and resuspended in Tris buffer containing 1 mM Ca[Cl.sub.2]. The aliquot was mixed vigorously with 10% trichloroacetic acid solution and TAE buffer (100 mM Tris-acetate, 2 mM EDTA, pH 7.8) and then cooled on ice for 20 min. The sample was centrifuged, and the aliquot of resultant supernatant was mixed with cold TAE buffer. Samples were adapted to the luciferin/luciferase assay in a Luminoskan microplate reader (Labsystems, Franklin, MA, USA) using an ATP assay kit (Sigma). We calculated the ATP concentrations based on the ATP standard curve.

Protein thiol level measurement. We determined protein thiol concentrations using a modified assay based on the colorimetric method described by Di Monte et al. (1984). After incubation with various concentrations of [Hg.sup.2+], erythrocytes were centrifuged at 7,000 x g for 1 min, and the supernatant was removed. The pellet was resuspended with lysis buffer (5 mM sodium phosphate, pH 8) and incubated on ice for 30 min. Total lysate was resuspended with 5% perchloric acid 2:5 and then centrifuged at 7,000 x g for 2 min. The pellet was solubilized in 1 mL Tris-EDTA buffer (0.5 mM Tris-HCl, 5 mM EDTA, pH 7.6) containing 1% sodium dodecyl sulfate. 5,5'-Dithio-bis-(2-nitrobenzoic acid) (DTNB; 250 [micro]M) was added to the samples, and the change of absorbance was measured at 412 nm. The content of protein thiol was calculated on the basis of a glutathione calibration curve and divided by the protein content, which was measured by Bio-Rad protein assay kit (Bio-Rad, Hercules, CA, USA).

Prothrombinase assay. After incubation with [Hg.sup.2+] for 4 hr, erythrocytes were incubated with 5 nM factor Xa and 10 nM factor Va (both from Hematologic Technologies Inc., Essex Junction, VT, USA) in Tyrode buffer (134 mM NaCl, 10 mM HEPES, 5 mM glucose, 2.9 mM KC1, 1 mM [MgCl.sub.2], 12 mM NaHC[O.sub.3], 0.34 mM [Na.sub.2][HPO.sub.4], 0.3% BSA, 2 mM [CaCl.sub.2], pH 7.4) for 3 min at 37[degrees]C. Thrombin formation was initiated by adding 2 [micro]M prothrombin. Exactly 3 min after addition of prothrombin, an aliquot of the suspension was transferred to a tube containing stop buffer (50 mM Tris-HCl, 120 mM NaCl, 2 mM EDTA, pH 7.9). Thrombin activity was determined using the chromogenic substrate S2238 (chromogenic substrate for thrombin; Chromogenix, Milano, Italy). We calculated the rate of thrombin formation from the change in absorbance at 405 nm using a calibration curve generated with active-site-titrated thrombin.

Measurement of thrombin generation in plasma. We measured thrombin generation in plasma according to the method described by Peyrou et al. (1999). Briefly, Tris buffer- or [Hg.sup.2+]-treated erythrocytes were added to plasma, and under gentle magnetic stirring, thrombin formation was initiated by adding human recombinant tissue factor (Recombiplastin; Instrumentation Laboratory, Lexington, MA, USA) diluted (1:3,200) in Tris buffer containing 100 mM Ca[Cl.sub.2] to the mixture. After 10 min, the aliquots were collected and transferred to Trisbuffer containing 20 mM EDTA. The thrombin concentration was obtained as described above for the prothrombinase assay.

Adherence of erythrocytes to human umbilical vein endothelial cells (HUVEC). The HUVEC (three passages) were maintained in EGM (endothelial cell growth media) kit (Clonetics, Walkersville, MD) at 37[degrees]C in a 95% air/5% [CO.sub.2] incubator. Before the experiments, 1 x [10.sup.5] cells were seeded into a T25 flask and grown for 5 days. Erythrocyte adherence to HUVEC was measured using a modification of the method described by Chung et al (2007). PBS- or [Hg.sub.2+]-treated erythrocytes were washed twice and resuspended in endothelial basal medium (EBM)-2 (Clonetics) to a cell concentration of 5 x [10.sup.7] cells/mL. After HUVEC were washed twice with EBM-2 to remove media, the erythrocytes were layered onto a confluent HUVEC monolayer and incubated for 45 min at 37[degrees]C. After the incubation, the flask was rinsed three times with EBM-2 to remove nonadherent erythrocytes. The number of adherent erythrocytes was counted on a light microscope. The experiments were performed in triplicate, and 28 fields were selected randomly for counting erythrocytes.

Ex vivo PS exposure measurement and venous thrombosis animal model We used male Sprague-Dawley rats (SamTako Co., Osan, Korea) weighing 180-250 g for animal studies. For the measurement of PS exposure, animals were injected intravenously with saline (vehicle) or Hg[Cl.sub.2] (bolus, 1.0 and 2.5 mg/kg/0.3 mL) into a left femoral vein; 1 hr later blood was collected from the abdominal aorta using 3.8% trisodium citrate as anticoagulant. An aliquot of the blood sample was diluted 200-fold with buffer (10 mM HEPES-Na, 136 mM NaCl, 2.7 mM KCl, 2.0 mM Mg[Cl.sub.2], 1.0 mM Na[H.sub.2][PO.sub.4], 5.0 mM dextrose, 5 mg/mL BSA, 2.5 mM Ca[Cl.sub.2], pH 7.4) and stained with annexin V-FITC for 15 min in the dark. PS exposure was measured as described above.

Venous thrombosis was induced by stasis combined with hypercoagulability. Rats (180-250 g body weight) were anesthetized with intraperitoneal urerthane (1.25 g/kg), the abdomen was surgically opened, and the vena cava was exposed. Two loose cotton threads were prepared around the vena cava 16 mm apart, and all side branches were ligated tightly with cotton threads. One hour after intravenous injection of saline or Hg[Cl.sub.2] (bolus, 0.25, 0.5, or 1.0 mg/kg/0.3 mL) into a left femoral vein, 1,000-fold diluted thromboplastin was infused to induce thrombus formation. Stasis was initiated by tightening the two threads, first the proximal one, and 30 sec later the distal one. The abdominal cavity was provisionally closed, and blood stasis was maintained for 15 min. After the abdomen was reopened, the ligated venous segment was excised and opened longitudinally to remove the thrombus. The isolated thrombus was blotted of excess blood and immediately weighed.

Statistical analysis. We calculated mean [+ or -] SE for all treatment groups. The data were subjected to one-way analysis of variance followed by Duncan's multiple range test to determine which means were significantly different from control. In all cases, p < 0.05 indicated significance.


To investigate the effects of mercury on erythrocytes, we examined the shape change in erythrocytes after exposure to 5 [micro]M Hg[Cl.sub.2] using SEM. As shown in Figure 1A, normal discocytic shapes changed into echinocytic erythrocytes and further into spherocytes, depending on the length of exposure to [Hg.sup.2+]. It is well known that erythrocytes change into spherocytes by a substantial loss of membrane surface through vesiculation and MV generation. To visually identify MV generation, we treated erythrocytes attached to a poly-Llysine--coated coverslip chamber with [Hg.sup.2+] and observed them under confocal microscopy using erythrocyte-specific anti--glycophorin-A--FITC. [Hg.sup.2+] treatment induced typical MV generation on erythrocyte membranes (Figure 1B, right). In flow cytometry analysis, MV generation increased in a time- and concentration-dependent manner after [Hg.sup.2+] incubation (Figure 1C,D).

MVs bearing PS can display procoagulant activity. In the flow cytometry analysis with annexin V-FITC to specifically detect PS, MVs generated by [Hg.sup.2+] treatment expressed PS in their outer membranes (Figure 2A). Moreover, remnant erythrocytes also expressed PS in the outer membrane (62.2 [+ or -] 11.2% at 5 [micro]M [Hg.sup.2+]; Figure 2B), consistent with the report by Eisele et al. (2006). PS expression also increased in a time-dependent manner with [Hg.sup.2+] (Figure 2B, inset), and of particular note, prolonged exposure induced significant PS expression even at lower concentrations of [Hg.sup.2+] (down to 0.25 [micro]M; Figure 2C). To investigate the mechanism underlying [Hg.sup.2+]-induced PS exposure and MV generation, we evaluated the activities of representative aminophospholipid translocases governing lipid asymmetry. We measured flippase, an enzyme that recovers PS into the inner leaflet of the cell membrane, and scramblase, an enzyme that disrupts lipid asymmetry in the cell membrane, based on the extent of [C.sub.6]-NBD-PS and [C.sub.6]-NBD-PC translocation, respectively, after incubation of [Hg.sup.2+]. [C.sub.6]-NBD-PS and [C.sub.6]-NBD-PC are the fluorescent analogs of PS and phosphatidylcholine; we measured the internalization of [C.sub.6]-NBD-PS and [C.sub.6]-NBD-PC by flippase and scramblase, respectively, by comparing the fluorescence intensity associated with the cells before and after BSA back-extraction, as described in "Materials and Methods." As shown in Figure 2D and E, flippase was inhibited by [Hg.sup.2+], whereas scramblase was activated in a concentration-dependent manner, which explains [Hg.sup.2+]-induced PS exposure.

Increased intracellular calcium can mediate concomitant inhibition of flippase and activation of scramblase, leading to the disruption of membrane lipid asymmetry (Daleke 2003). To investigate whether [Hg.sup.2+] treatment can induce calcium increase, we incubated Fluo-4--loaded erythrocytes with [Hg.sup.2+] and measured intracellular calcium increase by flow cytometry analysis. As shown in Figure 3A, [Hg.sup.2+] treatment increased intracellular calcium prominently, up to 10 times the basal level. For this calcium signal, an artifactual increase due to possible interference with Fluo-4 binding by [Hg.sup.2+] could be excluded by adding the [Hg.sup.2+] quencher TPEN, a high-affinity membrane-permeable intracellular heavy metal chelator (Arslan et al. 1985). ATP depletion, which can prompt flippase inhibition, was also induced by [Hg.sup.2+] (Figure 3B). In general, [Hg.sup.2+]-induced cytotoxicity is mediated by thiol depletion (Zalups 2000) or oxidative stress (Wiggers et al. 2008). To examine the role of thiol depletion and oxidative stress in [Hg.sup.2+]-induced PS exposure and MV generation, we preincubated erythrocytes with the thiol supplements N-acetylcysteine and dithio-threitol (DTT) or the antioxidant Trolox. As shown in Figure 3C, Trolox was marginally effective, whereas thiol supplements effectively blocked [Hg.sup.2+]-induced PS exposure and MV generation, indicating a major role of thiol depletion. Indeed, [Hg.sup.2+] treatment induced significant thiol depletion (Figure 3E). In line with these findings, thiol supplementation prevented [Hg.sup.2+]-induced ATP depletion and [Ca.sup.2+] increase (Figure 3F), indicating that [Hg.sup.2+] induces PS exposure and MV generation in erythrocytes through protein-thioldepletion--mediated ATP depletion and [Ca.sup.2+] increases.

We confirmed prothrombotic effects of [Hg.sup.2+]-induced PS exposure and MV generation by evidence of increased thrombin generation based on the prothrombinase assay and thrombin generation in plasma (Figure 4A,B). Moreover, we demonstrated increased adherence of [Hg.sup.2+]-exposed erythrocytes to endothelial cells by increased erythrocyte adhesion on HUVEC (Figure 4C). To evaluate the in vivo relevance of [Hg.sup.2+]-induced procoagulant activity in erythrocytes, we used rat ex vivo PS exposure measurement and in vivo venous thrombosis models. Before the in vivo experiments, we confirmed PS exposure and MV generation by [Hg.sup.2+] in rat erythrocytes (Figure 5A), which showed a pattern similar to that of human erythrocytes. Confirming these in vitro results, treatment of Hg[Cl.sub.2] [intravenous bolus 0.25-2.5 mg/kg (0.92-9.2 [micro]mol/kg)] induced PS exposure on erythrocytes ex vivo (Figure 5B; 2.1 [+ or -] 0.2% for 1 mg/kg and 3.4 [+ or -] 0.7% for 2.5 mg/kg Hg[Cl.sub.2] vs. 1.4 [+ or -] 0.1% for vehicle; p < 0.05) and promoted clot formation in a stasis- and hypercoagulability-induced venous thrombosis model after thromboplastin infusion (Figure 5C; 12.2 [+ or -] 1.0 mg for 0.5 mg/kg Hg[Cl.sub.2] and 16.9 [+ or -] 2.3 mg for 1 mg/kg Hg[Cl.sub.2] vs. 2.4 [+ or -] 1.7 mg for vehicle; p < 0.01), suggesting that [Hg.sup.2+]-induced procoagulant activity in erythrocytes could contribute to increased thrombosis in vivo.


In this study, we demonstrated that [Hg.sup.2+] can induce shape changes, MV generation, and PS exposure on erythrocytes, important mediators of procoagulant activation of erythrocytes. [Hg.sup.2+]-mediated thiol depletion was responsible for calcium increase--mediated and ATP depletion--mediated flippase inhibition and scramblase activation, leading to increased thrombin generation, enhanced adhesion of erythrocytes to endothelial cells, and ultimately, accelerated thrombus formation (Figure 6). Of particular note, ex vivo PS exposure measurement and the rat in vivo venous thrombosis model confirmed the procoagulant effect of [Hg.sup.2+] by demonstrating increased PS exposure and clot formation, suggesting that procoagulant activation of erythrocytes might contribute to CVDs associated with mercury exposure.

Erythrocytes can contribute to hemostasis and thrombosis through procoagulant activation via PS exposure and MV generation (Zwaal et al. 2005; Zwaal and Schroit 1997). Endogenous thrombogenic substances such as arachidonic acid, lysophos-phatidic acid, and thromboxane are known to induce PS exposure on erythrocyte surfaces (Chung et al. 2007; Valles et al. 2002). In addition, we previously demonstrated that lead, another toxic heavy metal, can induce a substantial level of PS exposure in erythrocytes and that this procoagulant activity manifested as enhanced thrombus formation (Shin et al. 2007). Interestingly, it is well known that erythrocytes can be a preferential store for toxic heavy metals. Methylmercury accumulates in erythrocytes at a concentration > 20 times that of plasma (Clarkson 2002), and 90% of body lead is associated with erythrocytes. These findings suggest that erythrocytes can be a common target for CV toxicity of heavy metals; thus, the role of erythrocytes in CV toxicity of heavy metals should be more closely investigated.

Millimolar concentrations of [Hg.sup.2+] have been reported to induce shape changes and hemolysis in erythrocytes (Suwalsky et al. 2000; Zolla et al. 1997). The concentration employed in those studies, however, was unrealistically high, considering reported human exposure levels even in highly contaminated areas. In the present study, however, we discovered that longer exposure to concentrations of [Hg.sup.2+] as low as 0.25 [micro]M can induce shape changes and procoagulant activation in erythrocytes as determined by increased PS exposure. The highest blood mercury concentrations reported in humans were in workers in the gold mines of the Amazon area (Akagi et al. 1995), whose blood mercury levels were as high as 150 [micro]g/L (~ 0.75 [micro]M). Wierzbicki et al. (2002) reported that workers occupationally exposed to mercuric vapors exhibited a statistically significant increase in blood coagulation along with increased thrombin generation. Their average plasma mercury levels were approximately 0.03-0.04 [micro]M but measured as high as 83.3 [micro]g/L (0.4 [micro]M). Virtanen et al. (2005) observed increased CV events in a mercury-exposed population with an average hair mercury level of 1.9 [micro]g/g (0-15.7 [micro]g/g), which is estimated to indicate a blood mercury level of 9.5 [micro]g/L (0.05 [micro]M) based on a 200:1 hair-to-blood mercury ratio (Budtz-Jorgensen et al. 2004). These levels are within an order of magnitude of the mercury concentrations used in our study, suggesting that mercury-induced procoagulant activation of erythrocytes might indeed contribute to the increased CVDs in human populations. However, because we conducted our study with only [Hg.sup.2+], further in vivo studies with methylmercury or elemental mercury are needed to fully clarify the link between mercury-mediated procoagulant activation of erythrocytes and mercury-associated CVDs.

Adding to the previous report on [Hg.sup.2+]-induced echinocytic changes in human erythrocytes (Suwalsky et al. 2000), we found that echinocytes can be further progressed into spherocytes (Figure 1A) by prolonged exposure to [Hg.sup.2+]. Moreover, along with these remarkable shape changes, substantial numbers of MVs can be liberated from erythrocytes. Apart from clot-promoting activity in plasma, MV generation can result in decreased deformability of erythrocytes (Chabanel et al. 1989; Chasis and Mohandas 1986; Mentzer et al. 1987) and, more important, PS-exposing MVs provide sites for adhesion of platelets and neutrophils by localizing at the subendothelium, indicating that [Hg.sup.2+]-induced MV generation can contribute to the prothrombotic effects of mercury exposure.

In our study, we determined thiol depletion to be a key mediator for calcium increase, ATP depletion, PS exposure, and MV generation in erythrocytes by [Hg.sup.2+]. Thiol depletion by [Hg.sup.2+] can be well explained by the strong thiol-binding affinity of nucleophilic [Hg.sup.2+] (Casarett et al. 2007). Intracellular molecules with free sulfhydryl groups, such as glutathione, cysteine, and metallothionein, can be easy targets for [Hg.sup.2+] binding, and free thiol groups of intracellular proteins, which are vital to the maintenance of erythrocyte integrity (e.g., of the cytoskeleton) and ionic balance (e.g., [Na.sup.2+]/[K.sup.+]-ATPase), can be readily modified by thiol-depleting agents, leading to a increased fragility of the erythrocyte membrane and disruption of ionic homeostasis. Moreover, depletion of free thiols in cells can cause depletion of ATP, inhibition of flippase (Daleke and Lyles 2000), and increased calcium, consistent with the result of the present study.


We demonstrated that low-dose mercury can induce thrombogenic PS exposure and MV generation through thiol-depletion--mediated ATP depletion and calcium increase in erythrocytes. As shown by increased PS exposure and clot formation in vivo, mercury-induced procoagulant activation of erythrocytes might contribute to enhanced thrombosis in the population exposed to mercury, providing an important clue for the elucidation for the CVDs associated with mercury.


Agency for Toxic Substances and Disease Registry. 2007. Toxicological Profile for Mercury. Atlanta, GA:Agency for Toxic Substances and Disease Registry.

Akagi H, Malm O, Branches FJP, Kinjo Y, Kashima Y, Guimaraes JRD, et al. 1995. Human exposure to mercury due to goldmining in the Tapajos River basin, Amazon, Brazil: speciation of mercury in human hair, blood and urine. Water Air Soil Pollut 80:85-94.

Arslan P, Di Virgilio F, Beltrame M, Tsien RY, Pozzan T. 1985. Cytosolic [Ca.sup.2+] homeostasis in Ehrlich and Yoshida carcinomas. A new, membrane-permeant chelator of heavy metals reveals that these ascites tumor cell lines have normal cytosolic free [Ca.sup.2+]. J Biol Chem 260:2719-2727.

Berglund M, Lind B, Bjornberg K, Palm B, Einarsson O, Vahter M. 2005. Inter-individual variations of human mercury exposure biomarkers: a cross-sectional assessment. Environ Health 4:20; doi:10.1186/1476-069X-4-20 [Online 3 October 2005].

Berlin M, Zalups RK, Fowler BA, Gunnar FN, Bruce AF, Monica N, et al. 2007. Mercury. In: Handbook on the Toxicology of Metals. 3rd ed. Burlington, VT:Academic Press, 675-729.

Budtz-Jorgensen E, Grandjean P, Jorgensen PJ, Weihe P, Keiding N. 2004. Association between mercury concentrations in blood and hair in methylmercury-exposed subjects at different ages. Environ Res 95:385-393.

Casarett LJ, Klaassen CD, Doull J. 2007. Casarett and Doull's Toxicology: The Basic Science of Poisons. 7th ed. New York:McGraw-Hill

Chabanel A, Sung KL, Rapiejko J, Prchal JT, Palek J, Liu SC, et al. 1989. Viscoelastic properties of red cell membrane in hereditary elliptocytosis. Blood 73:592-595.

Chasis JA, Mohandas N. 1986. Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations. J Cell Biol 103:343-350.

Chung SM, Bae ON, Lim KM, Noh JY, Lee MY, Jung YS, et al. 2007. Lysophosphatidic acid induces thrombogenic activity through phosphatidylserine exposure and procoagulant microvesicle generation in human erythrocytes. Arterioscler Thromb Vasc Biol 27:414-421.

Clarkson TW. 2002. The three modern faces of mercury. Environ Health Perspect 110(suppl 1):11-23.

Clarkson TW, Magos L, Myers GJ. 2003. The toxicology of mercury--current exposures and clinical manifestations. N Engl J Med 349:1731-1737.

Closse C, Dachary-Prigent J, Boisseau MR. 1999. Phosphatidylserine-related adhesion of human erythrocytes to vascular endothelium. Br J Haematol 107:300-302.

Daleke DL. 2003. Regulation of transbilayer plasma membrane phospholipid asymmetry. J Lipid Res 44:233-242.

Daleke DL, Lyles JV. 2000. Identification and purification of aminophospholipid flippases. Biochim Biophys Acta 1486:108-127.

Di Monte D, Bellomo G, Thor H, Nicotera P, Orrenius S. 1984. Menadione-induced cytotoxicity is associated with protein thiol oxidation and alteration in intracellular [Ca.sup.2+] homeostasis. Arch Biochem Biophys 235:343-350.

Eisele K, Lang PA, Kempe DS, Klarl BA, Niemoller O, Wieder T, et al. 2006. Stimulation of erythrocyte phosphatidylserine exposure by mercury ions. Toxicol Appl Pharmacol 210:116-122.

Environment Canada. 2004. Mercury and the Environment: Sources of Mercury. Available: [accessed 1 June 2010].

Hilarius PM, Ebbing IG, Dekkers DW, Lagerberg JW, de Korte D, Verhoeven AJ. 2004. Generation of singlet oxygen induces phospholipid scrambling in human erythrocytes. Biochemistry 43:4012-4019.

Houston MC. 2007. The role of mercury and cadmium heavy metals in vascular disease, hypertension, coronary heart disease, and myocardial infarction. Altern Ther Health Med 13:S128-S133.

Macfarlane DE. 1981. The effects of methyl mercury on platelets: induction of aggregation and release via activation of the prostaglandin synthesis pathway. Mol Pharmacol 19:470-476.

Mahaffey KR, Mergler D. 1998. Blood levels of total and organic mercury in residents of the upper St. Lawrence River Basin, Quebec: association with age, gender, and fish consumption. Environ Res 77:104-114.

Martinez MC, Tesse A, Zobairi F, Andriantsitohaina R. 2005. Shed membrane microparticles from circulating and vascular cells in regulating vascular function. Am J Physiol Heart Circ Physiol 288:H1004-H1009.

McKelvey W, Gwynn RC, Jeffery N, Kass D, Thorpe LE, Garg RK, et al. 2007. A biomonitoring study of lead, cadmium, and mercury in the blood of New York City adults. Environ Health Perspect 115:1435-1441.

Mentzer WC Jr, larocci TA, Mohandas N, Lane PA, Smith B, Lazerson J, et al. 1987. Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome. J Clin Invest 79:943-949.

Peyrou V, Lormeau JC, Herault JP, Gaich C, Pfliegger AM, Herbert JM. 1999. Contribution of erythrocytes to thrombin generation in whole blood. Thromb Haemost 81:400-406.

Rodrigues JL, de Souza SS, de Oliveira Souza VC, Barbosa F Jr. 2010. Methylmercury and inorganic mercury determination in blood by using liquid chromatography with inductively coupled plasma mass spectrometry and a fast sample preparation procedure. Talanta 80:1158-1163.

Salonen JT, Seppanen K, Lakka TA, Salonen R, Kaplan GA. 2000. Mercury accumulation and accelerated progression of carotid atherosclerosis: a population-based prospective 4-year follow-up study in men in eastern Finland. Atherosclerosis 148:265-273.

Shin JH, Lim KM, Noh JY, Bae ON, Chung SM, Lee MY, et al. 2007. Lead-induced procoagulant activation of erythrocytes through phosphatidylserine exposure may lead to thrombotic diseases. Chem Res Toxicol 20:38-43.

Suwalsky M, Ungerer B, Villena F, Cuevas F, Sotomayor CP. 2000. Hg[Cl.sub.2] disrupts the structure of the human erythrocyte membrane and model phospholipid bilayers. J Inorg Biochem 81:267-273.

Trasande L, Landrigan PJ, Schechter C. 2005. Public health and economic consequences of methyl mercury toxicity to the developing brain. Environ Health Perspect 113:590-596.

Valera B, Dewailly E, Poirier P. 2008. Cardiac autonomic activity and blood pressure among Nunavik Inuit adults exposed to environmental mercury: a cross-sectional study. Environ Health 7:29; doi:10.1186/1476-069X-7-29 [Online 6 June 2008].

Valles J, Santos MT, Aznar J, Martinez M, Moscardo A, Pinon M, et al. 2002. Platelet-erythrocyte interactions enhance alpha(IIb)beta(3) integrin receptor activation and

P-selectin expression during platelet recruitment: down-regulation by aspirin ex vivo. Blood 99:3978-3984.

Virtanen JK, Rissanen TH, Voutilainen S, Tuomainen TP. 2007. Mercury as a risk factor for cardiovascular diseases. J Nutr Biochem 18:75-85.

Virtanen JK, Voutilainen S, Rissanen TH, Mursu J, Tuomainen TP, Korhonen MJ, et al. 2005. Mercury, fish oils, and risk of acute coronary events and cardiovascular disease, coronary heart disease, and all-cause mortality in men in eastern Finland. Arterioscler Thromb Vasc Biol 25:228-233.

Wierzbicki R, Prazanowski M, Michalska M, Krajewska U, Mielicki WP. 2002. Disorders in blood coagulation in humans occupationally exposed to mercuric vapors. J Trace Elem Exp Med 15:21-29.

Wiggers GA, Pecanha FM, Briones AM, Perez-Giron JV, Miguel M, Vassallo DV, et al. 2008. Low mercury concentrations cause oxidative stress and endothelial dysfunction in conductance and resistance arteries. Am J Physiol Heart Circ Physiol 295:H1033-H1043.

Zalups RK. 2000. Molecular interactions with mercury in the kidney. Pharmacol Rev 52:113-143.

Zolla L, Lupidi G, Bellelli A, Amiconi G. 1997. Effect of mercuric ions on human erythrocytes. Relationships between hypotonic swelling and cell aggregation. Biochim Biophys Acta 1328:273-280.

Zwaal RF, Comfurius P, Bevers EM. 2005. Surface exposure of phosphatidylserine in pathological cells. Cell Mol Life Sci 62:971-988.

Zwaal RF, Comfurius P, van Deenen LL. 1977. Membrane asymmetry and blood coagulation. Nature 268:358-360.

Zwaal RF, Schroit AJ. 1997. Pathophysiologic implications of membrane phospholipid asymmetry in blood cells. Blood 89:1121-1132.

Address correspondence to J.H. Chung, College of Pharmacy, Seoul National University, Shinrim-dong San 56-1, Seoul 151-742, Korea. Telephone: 82-2-880-7856. Fax: 82-2-885-4157. E-mail:

* Current address: R&D Center, Amorepacific Co., Gyeonggi-do 446-729, Korea.

** These authors contributed equally to this work.

This research was supported by a grant from the Korea Food & Drug Administration.

The authors declare they have no actual or potential competing financial interests.

Received 6 September 2009; accepted 12 March 2010.

Kyung-Min Lim, *, ** Sujin Kim, *, ** Ji-Yoon Noh, Keunyoung Kim, Won-Hee Jang, Ok-Nam Bae, Seung-Min Chung, and Jin-Ho Chung

College of Pharmacy, Seoul National University, Seoul, Korea
COPYRIGHT 2010 National Institute of Environmental Health Sciences
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2010 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:Research
Author:Lim, Kyung-Min; Kim, Sujin; Noh, Ji-Yoon; Kim, Keunyoung; Jang, Won-Hee; Bae, Ok-Nam; Chung, Seung-M
Publication:Environmental Health Perspectives
Article Type:Report
Geographic Code:9SOUT
Date:Jul 1, 2010
Previous Article:A comparison of vascular effects from complex and individual air pollutants indicates a role for monoxide gases and volatile hydrocarbons.
Next Article:Mot-2--mediated cross talk between nuclear factor-KB and p53 is involved is arsenite-induced tumorigenesis of human embryo lung fibroblast cells.

Terms of use | Copyright © 2017 Farlex, Inc. | Feedback | For webmasters