Changes in [Ca²⁺]_i

The results are shown in Table 1, Fig. 1A. The average [Ca²⁺]_i were 502.32±135.25, 748.06±249.27, 1171.11±189.12 and 1673.94±223.02 nmol/10⁶ sperm in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively. The average [Ca²⁺]_i rose with increasing concentration of HBs. A marked significant increases in average [Ca²⁺]_i were observed after 3 h exposure to 50 and 100 µg/ml of HBs as compared to that in control (P<0.01).

Download:

• PPT
  PowerPoint slide
• PNG
  larger image
• TIFF
  original image

Figure 1. HBs induced early apoptotic events in human spermatozoa.

A: The average [Ca²⁺]_i rose with increasing concentrations of HBs. There are marked significant differences in the average [Ca²⁺] _i in 50 µg/ml and 100 µg/ml HBs groups when compared with that in the control (P<0.01). The high levels of [Ca²⁺] _i induced by HBs would be a signal to trigger apoptosis. B: In contrast, FI of Cal-AM declined with increasing concentrations of HBs. There are significant differences in FI between the control and test groups (P<0.05). This suggested that MPTP opening has occurred, and the extent of pore opening increased with increasing concentrations of HBs. C: the levels of cyt c in mitochondria fractions declined with increasing concentrations of HBs, in parallel, the levels of cyt c in cytosolic fractions rose with increasing concentrations of HBs. There are significant differences in levels of cyt c in all test groups as compared to that in control (P<0.05 or P<0.01). This suggested that cyt c was released from mitochondria to cytoplasm through the MPTP. D: The ADP/ATP ratio rose with increasing concentrations of HBs. There are significant differences in ADP/ATP ratio between the control and all test groups (P<0.01). It indicated that spermatozoa underwent apoptosis induced by HBs. In all above events, effects of HBs exposure on spermatozoa showed dose dependency.

https://doi.org/10.1371/journal.pone.0068688.g001

Download:

• PPT
  PowerPoint slide
• PNG
  larger image
• TIFF
  original image

Table 1. Effects of HBs exposure on early apoptotic events in human spermatozoa.

https://doi.org/10.1371/journal.pone.0068688.t001

Assessment of MPTP

In the individual experiment, the fluorescent intensities (FI) of Cal-AM in spermatozoa were 409.56, 334.75, 264.09 and 105.47 in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively (Fig. 2). In five experiments, the average FI of Cal-AM in spermatozoa were 433.59±119.47, 356.06±96.87, 291.64±80.31 and 214.66±73.7 in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively (Table 1, Fig. 1B). The FI of Cal-AM in spermatozoa, either its single value or its average value, declined with increasing concentration of HBs (Fig. 1 and 2), and the number of spermatozoa showing diminished fluorescence rose with increasing concentration of HBs (Fig. 2). There were significant differences in average FI of Cal-AM in all test groups as compared to that in control (P<0.05).

Download:

• PPT
  PowerPoint slide
• PNG
  larger image
• TIFF
  original image

Figure 2. HBs induced MPTP activation in human spermatozoa.

The histograms of the number of events (Y-axis) versus the FI (X-axis) in the individual experiment showed that FI of Cal-AM in spermatozoa declined with increasing concentration of HBs, and the number of spermatozoa showing diminished FI rose with increasing concentration of HBs. The change in FI Cal-AM in spermatozoa between panels indicates the continuous activation of MPTP.

https://doi.org/10.1371/journal.pone.0068688.g002

Assessment of Cyt c Release from Mitochondria

The levels of cyt c in mitochondrial fraction were 124.95±10.47, 109.69±9.17, 89.58±10.78, 74.44±11.16 ng/mg in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively. In parallel, the levels of cyt c in cytosolic fraction were 5.04±1.52, 13.01±2.5, 27.73±6.75 and 49.66±8.12 ng/mg in the above groups, respectively. The levels of cyt c decreased in mitochondrial fraction and increased in cytosolic fraction with increasing concentration of HBs (Table 1, Fig. 1C). There were significant differences in average levels of cyt c in all test groups when compared with that in control (P<0.05 and P<0.01).

The ADP/ATP Ratio

The ADP/ATP ratios in spermatozoa were 0.04±0.02, 0.27±0.05, 0.48±0.04 and 0.83±0.05 in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively, and rose with increasing concentrations of HBs (Table 1, Fig. 1D). There were significant differences in ADP/ATP ratio in all test groups as compared to that in control (P<0.01).

Sperm Motility Parameters

The average rates (%) of total motility (MOT) were 85.80±4.04, 82.40±3.42, 73.40±3.59 and 65.40±3.09 in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively, and the mean hyperactivation (HA) rates (%) were 45.00±11.00, 36.00±8.00, 30.00±6.00 and 19.00±4.00 in the above groups, respectively. The average rate of MOT and the mean HA rate declined with increasing concentrations of HBs (Fig. 3A and 3B). There were significant differences in the average rates of MOT in 50 and 100 µg/ml HBs-exposed groups and in the mean HA rates in all test groups when compared with those in controls (P<0.05 and P<0.01). The sperm velocities including VSL, VCL and VAP in the above groups declined with increasing concentrations of HBs. There were significant differences in VSL and VCL in 100 µg/ml HBs group and in VAP in all test groups when compared with those in controls (Fig. 3D, 3E and 3F). The significant differences in other parameters including concentration (CON), progressive motility (PMOT), straightness (STR), linearity (LIN), amplitude of lateral head displacement (ALH) and beat cross frequency (BCF) among the above groups have not been observed.

Download:

• PPT
  PowerPoint slide
• PNG
  larger image
• TIFF
  original image

Figure 3. Effects of HBs exposure on sperm fertilizing capacity.

A and B: The average rates of MOT and the mean HA rates declined with increasing concentrations of HBs. There were significant differences in the average rates of MOT in 50 and 100 mg/ml HBs groups and in the mean HA rates in all test groups when compared with those in the controls (P<0.05 or P<0.01). C: The average rates (%) of ZPIAR declined with increasing concentrations of HBs. There were marked significant differences in ZPIAR rates in all test groups as compared to that in control (P<0.01). D–F: The sperm velocities including VSL, VCL and VAP declined with increasing concentrations of HBs. There were significant differences in VSL and VCL in 100 mg/ml HBs group and in VAP in all test groups when compared with those in controls. The above results showed that HBs exposure could affect sperm fertilizing capacity.

https://doi.org/10.1371/journal.pone.0068688.g003

Sperm-ZP Binding

The medians in number of sperms bound to ZP were 100 in the 0, 25, 50, 100 µg/ml HBs-exposed groups, and their quartile deviations were 30, 25, 30, 30 in the above groups, respectively. There was no significant difference in number of sperms bound to ZP between any of the four groups (P>0.05).

Assessment of the AR of Sperms Bound to the ZP

The average rates (%) of ZPIAR were 38.36±8.73, 28.57±11.76, 18.99±6.84 and 10.98±3.58 in 0, 25, 50, 100 µg/ml HBs-exposed groups, respectively, and declined with increasing concentrations of HBs (Fig. 3C). There were marked significant differences in ZPIAR rates in all test groups as compared to that in control (P<0.01).

HBs Induced Early Apoptotic Events in Human Spermatozoa

Recent publications have suggested that mitochondria of human spermatozoa are preferentially susceptible to apoptosis in response to various types of intracellular stress [14]. One of the responsible signals for initiating the process of apoptosis is a sustained increase in [Ca²⁺]_i [8]. In the present study, the average [Ca²⁺]_i in spermatozoa rose with increasing concentration of HBs. Significant increases in average [Ca²⁺]_i were observed after 3 h exposure to 50 and 100 µg/ml of HBs as compared to that in control (P<0.01). This suggested that HBs exposure induced the entry of calcium ions into cells through the plasma membrane or release of Ca²⁺ from internal stores, leading to the elevation of [Ca²⁺]_i in spermatozoa. [Ca²⁺]_i was one of the signals initiating the process of apoptosis in this study.

[Ca²⁺]_i homeostasis is regulated by mitochondria, especially by MPTP, which is a nonspecific channel formed by components from the inner and outer mitochondrial membranes. Calcium enters the matrix via the mitochondrial Ca²⁺ uniporter and exits by exchange with Na⁺ on the Na^+/Ca²⁺ antiporter. Normally, MPTP may “flicker” to release excess matrix Ca²⁺ to maintain [Ca²⁺]_i homeostasis. However, when cells become pathologically overloaded with calcium, the MPTP opens irreversibly. Continuous MPTP activation causes mitochondrial Ca²⁺ overload, leading to mitochondrial dysfunction [15]. In the present study, the FI of Cal-AM in the spermatozoa declined with increasing concentration of HBs, and the number of spermatozoa showing diminished fluorescence rose with increasing concentration of HBs. There were significant differences in average FI of Cal-AM in all test groups as compared to that in control (P<0.05). Our results also revealed that HBs increased MPTP opening and the number of spermatozoa with pore opening in a dose-dependent manner. It has been reported that the sensitivity of MPTP to [Ca²⁺] is greatly enhanced by oxidative stress, phosphate and adenine nucleotide depletion [16], [17]. Our previous study has detected that HBs could induce oxidative stress in spermatozoa [13]. Therefore, HBs-induced MPTP opening could result from the synergistic effects of Ca²⁺ overload, ATP depletion and oxidative stress in this study.

Cyt c is a component of the electron transport chain in mitochondria and involved in initiation and is an intermediate of apoptosis. Activated MPTP releases cyt c from the intermembrane space into the cytoplasm. In the present study the average levels of cyt c declined in mitochondria fraction and rose in cytosolic fraction with increasing concentration of HBs. There were significant differences in average levels of cyt c in all test groups when compared with that in control (P<0.05 or P<0.01). This suggested that HBs exposure was able to induce release of cyt c from mitochondria to cytoplasm through the MPTP opening, and the higher the HBs concentration, the greater the amount of cyt c released.

Mitochondria are special energy-producing structures. Cells that are undergoing apoptosis or necrosis have more ADP compared to ATP because the cells are not producing ATP while hydrolyzing the remaining ATP into ADP. Thus, the changes in the ADP/ATP ratio have been used to differentiate the modes of cell death and viability. In the present study, the ADP/ATP ratios rose with increasing concentrations of HBs. There were significant differences in ADP/ATP ratios between control and all test groups (P<0.05, P<0.01). The levels of ADP, however, were still lower than ATP in the 100 µg/ml HBs-exposed group (0.83 vs 1.00), suggesting that only part of the mitochondria underwent opening of MPTP and the cell still had a sufficient level of ATP to direct cell death through the apoptotic pathway [18]. Thus, HBs led to spermatozoa apoptosis in this study.

In the present study, HBs exposure induced the early events in the apoptotic cascade. The induction of MPT by Ca²⁺ overload which increased mitochondrial membrane permeability, caused mitochondria to become further depolarized, meaning that MMP was abolished. This explains the mechanism through which HBs induced loss of MMP in our previous study [12]. Loss of MMP interferes with ATP production, because mitochondria must have an electrochemical gradient to provide the driving force for ATP production. Meanwhile, depolarization of mitochondria causes inhibition of oxidative phosphorylation and stimulation of ATP hydrolysis. That is why the ADP/ATP ratios rose with increasing concentrations of HBs in this study. When MMP is lost, protons and some molecules are able to flow across the outer mitochondrial membrane uninhibited [19], [20], leading to the release of apoptogenic proteins, such as cyt c, apoptosis-inducing factor and some pro-caspases, from the mitochondrial intermembrane space to cytoplasm [21], [17]. The released cyt c binds to apoptosis protease-activating factor 1 (Apaf-1) to form cyt c–Apaf-1 complex, which then activate caspase-9 [22], followed by activation of downstream death effectors such as caspase-3, caspase-6, and caspase-7 [23]. This can be used to explain our previous finding, in which HBs exposure was able to induce caspases-9, caspases-3 and caspases-8 activation in the spermatozoa [13].

However, an interesting question remains. How HBs triggers such responses in the spermatozoa? It has been demonstrated that the asialoglycoprotein receptor (ASGP-R) may play a role in the uptake of HBs into sperm cells [12]. The [Ca²⁺]_i was a signal initiating the process of apoptosis in this study. But it is still unknown how HBs induces Ca²⁺ overload after uptake into sperm cells, which should be further studied.

Effects of HBs Exposure on Sperm Fertilizing Capacity

Sperm motility is the ability of sperm to move properly towards an oocyte. Hyperactivation, a type of sperm motility, can facilitate sperm progression towards the oocyte and penetration of its vestments [24]–[26]. In the present study, the average rate of MOT and the mean HA rate declined with increasing concentrations of HBs. There were significant differences in the average rates of MOT in 50 and 100 µg/ml HBs-exposed groups and in the mean HA rates in all test groups when compared with those in controls (P<0.05 or P<0.01). The sperm velocity also deceased with increasing concentrations of HBs. This suggested that HBs exposure could affect sperm motility, velocity and hyperactivation and in a dose dependent manner. AR is an exocytotic process of spermatozoa and an absolute requirement for fertilization [27]. ZP is the main physiological inducer of AR [27], and the ZPIAR will enhance the ability of sperm to penetrate the ZP and finally to fertilize oocytes [28]. In the present study, the average rates of ZPIAR were reduced with increasing concentrations of HBs. There were significant differences in the average rates of ZPIAR between control and all test groups (P<0.05; P<0.01). Therefore HBs exposure could decrease the rates of ZPIAR in spermatozoa and showed dose-dependent toxicity.

It has been documented that Ca²⁺ is a primary second messenger and triggers hyperactivated motility in spermatozoa [25], [29], and Ca²⁺ influx is an absolute requirement for physiological AR in spermatozoa [30]. In the present study, the [Ca²⁺]_i in spermatozoa rose markedly with increasing concentration of HBs. Accordingly HBs-induced [Ca²⁺]_i increase should result in elevating MOT, hyperactivation and ZPIAR in this study. Why were they, on the contrary, lowered? The following reasons may contribute to this discrepancy. Calcium is a two-faced messenger, with different calcium levels causing diverse responses. Normally, spermatozoa become physiologically loaded with calcium, causing hyperactivated motility and ZPIAR. After exposure to HBs, the spermatozoa became pathologically overloaded with calcium, causing mitochondrial dysfunction, including MPTP opening and a cascade of subsequent apoptotic events, leading to the following consequences. Firstly, energy is necessary for spermatozoa to maintain the function during capacitation, hyperactivation, acrosome reaction and fertilization [31], [32]. The mitochondrial depolarization caused loss of MMP, leading to inhibition of ATP production. The reduced energy supply was unable to meet the requirements for initiating and maintaining above functions. Next, the membrane integrity is closely related to sperm motility, capacitation, acrosome reaction and sperm-oocyte interactions [33]. Our previous findings have demonstrated that HBs exposure could induce ROS generation, lipid peroxidation and PS externalization in spermatozoa [13]. Such apoptotic events are able to cause loss of membrane integrity, leading to reduced rates of motility, hyperactivation and acrosome reaction. Furthermore, the induction of acrosome reaction involves plasma membrane receptors, intracellular signals and signal transduction pathways, and is mediated by an increase in [Ca²⁺]_i. The calcium channels appear to be modulated either by plasma membrane potential or by protein phosphorylation [27]. All these involve integrity of sperm plasma membrane. When sperm loses membrane integrity, occurrence of acrosome reaction would be affected. Finally, the cyt c–Apaf-1 complex may play a role in lower sperm motility [34]. In fact, the opposing roles of calcium has been reported by some previous studies: on the one hand calcium is a key regulator of cell survival, on the other hand cellular Ca²⁺ overload, or perturbation of intracellular Ca²⁺ compartmentalization, can cause cytooxicity and trigger either apoptotic or necrotic cell death [35], [36].

In the present study, no significant difference in the number of sperms bound to ZP between control and test groups was found, suggesting that HBs exposure had no impact on binding of sperm to ZP.

In conclusion, exposure of HBs to human spermatozoa enhances the early events of apoptosis cascade and reduces sperm fertilizing capacity in vitro. This is an in vitro study, in which only mature and selected motile sperm were exposed to HBs. In the in vivo situation, sperms of a HBV-infected male will be exposed to the virus during spermatogenesis and afterwards. Both the testis and the epididymis will usually elicit an anti-viral immune response that should provide a certain level of protection absent in this in vitro situation. Thus, the in vivo impacts of HBs on male fertility require further investigation.

Ethical Approval

All healthy male donors and female patients, who were explicitly informed about the research aims, their rights and interests, signed consent forms permitting use of their gametes (sperm samples and unfertilized oocytes) for research. All the protocols used in the present study were approved by Institutional Ethical Review Board (IERB) of Shantou University Medical College (SUMC), and conformed to the ethical guidelines of the 1975 Declaration of Helsinki (The 6^th revision, 2008) as reflected in a priori approval by the institution’s human research committee.

Preparations of Human Spermatozoa

Human sperm samples were obtained from healthy men by masturbation after 3 days of sexual abstinence. Semen samples were kept in a humidified incubator (37°C, 5% CO₂ in air) for 30 min to allow liquefaction. Motile spermatozoa were selected by the swim-up method as follows: in each test tube, the 0.5 ml liquefied semen sample was layered gently under 2 ml of Biggers-Whittem-Whittingham (BWW) medium containing 0.3% bovine serum albumin (BSA) and incubated in a humidified incubator (37°C, 5% CO₂ in air) for 1 h. The supernatant collected from tubes was centrifuged at 300 × g for 5 min, and the pellet of motile sperm was washed once. The final concentration of spermatozoa was adjusted to 1×10⁶ sperm/ml in BWW medium with 0.3% BSA for subsequent use.

Exposure of Spermatozoa to HBs

Human spermatozoa were incubated in BWW medium with various concentrations of HBs (0, 25, 50, 100 µg/ml) (NCPC GencTech Biotechnology Co., LTD., Hebei, China) in a CO₂ incubator (37°C, 5% CO₂ in air) for 3 h, and then washed twice and adjusted to 1×10⁶ sperm/ml. The spermatozoa treated by HBs were used as test group, and the untreated spermatozoa were used as control group in the present study.

Preparations of Human Oocytes

Oocytes which showed no evidence of two pronuclei or cleavage at 48–60 h after insemination by routine in vitro fertilization (IVF), or after injection by intracytoplasmic sperm injection (ICSI), or immature (germinal vesicle or metaphase I) oocytes not injected by ICSI were used for the sperm–ZP binding test. If the oocytes had sperms bound to the ZP from the IVF insemination, these were removed by aspiration using a fine glass pipette with an inner diameter (120 µm) slightly smaller than the oocyte diameter [37]. Oocytes with >10 sperms penetrating the ZP, or degenerated, activated or morphologically abnormal were not used. Oocyte samples were stored in 1 M ammonium sulphate solution at 4°C before use. The salt-stored oocytes required extensive washing with culture medium over a period of 4 h to remove the salt before incubation with sperm.

Measurement of Changes in [Ca²⁺]_i

The changes in the [Ca²⁺]_i were monitored with the fluorescent probe fluo-4 AM which is a high-affinity calcium indicator. The motile spermatozoa, prepared as mentioned above, were pre-incubated with 10 µM fluo-4 AM (Dojindo) containing 0.1% pluronic acid F-127 in a dark chamber in a humidified incubator (37°C, 5% CO₂ in air) for 40 min followed by incubation with various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h. The cells were washed twice and resuspended in 0.5 ml of phosphate buffered saline (PBS), and immediately analyzed by using flow cytometry (FCM) with laser excitation wavelength at 488 nm and emission filter 522DF35. In order to convert fluorescence values into absolute [Ca²⁺]_i, the calibration was performed at the end of each experiment. [Ca²⁺]_i was calculated using the equation [Ca²⁺]_i = K_d (F − F_min)/(F_max − F), where K_d is the dissociation constant of the Ca²⁺-fluo-4 complex, and F represents the fluorescence intensity of the cells. F_max represents the maximum fluorescence (obtained by treating cells with 20 µM calcium ionophore A23187), and F_min corresponds to the minimum fluorescence (obtained from ionophore-treated cells in the presence of 3 mM EGTA). The above experiment was repeated five times.

Calcein/Co²⁺ Assay for MPTP Opening

Before exposure to HBs, the motile spermatozoa were loaded with Cal-AM (Dojindo, Kumamoto, Japan) to a final concentration of 15 µM in the presence of 30 µM CoCl₂ (Sigma-Aldrich, UK) and 0.1% Pluronic F127 in a dark chamber in a humidified incubator (37°C, 5% CO₂ in air). After 20 min incubation, the spermatozoa were washed twice with PBS to remove excess stain and quenching reagent, and then exposed to various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h. The sperm samples were analyzed by using FACScan Flow Cytometer (BD biosciences, San Diego, CA, USA) equipped with a single 488-nm argon-ion excitation laser. The above experiment was repeated five times.

FCM Analysis

FCM analyses were performed by using a FACScan Flow Cytometer (BD Biosciences, San Diego, CA). Cells were isolated from fragments by gating on the forward and side scatter signals, and then cells were identified and analyzed according to their relative fluorescence intensities compared with unstained cells. A minimum of 10,000 events were acquired and analyzed in each sample at the rate of 100–1000 events per second and data analysis was performed using BD Cell Quest and WinMDI 2.9. Results were expressed as mean fluorescence intensity.

Assessment of Cyt c Release from Mitochondria

After exposure of spermatozoa (1×10⁶/ml) to various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h, the preparation of cytosolic and mitochondrial fractions in spermatozoa were carried out by using Mitochondria/Cytosol Fractionation Kit (Catalog #K256, BioVision, CA, USA) according to the manufacturer’s instructions. Briefly, cells were washed with 10 ml of ice-cold PBS and centrifuged at 600×g for 5 min at 4°C. Supernatant was removed and cells resuspended with 1.0 ml of 1×Cytosol Extraction Buffer Mix containing DTT and protease inhibitors. Cells were incubated on ice for 10 min and homogenized in an ice-cold Dounce tissue grinder. After checking the efficiency of homogenization, homogenate was transferred to a 1.5-ml microcentrifuge tube, and centrifuged at 700×g for 10 min at 4°C. Supernatant was collected into a fresh 1.5-ml tube, and centrifuged at 10,000×g for 30 min at 4°C. This supernatant was stored as the cytosolic fraction. The pellet was resuspended in 0.1 ml Mitochondrial Extraction Buffer Mix containing DTT and protease inhibitors, vortexed for 10 s and saved as mitochondrial fraction.

The levels of cyt c in the cytosolic/mitochondria fractions were measured by using a Human Cytochrome c Quantikine ELISA Kit (R&D systems, Minneapolis, USA) according to the manufacturer’s instructions. ELISA was performed in triplicate (n = 3 per replicate) to calculate the average cyt c nanograms (ng) in the cytosolic or mitochondrial fractions per milligram (mg) of protein. The absorbance at 450 nm (a measure of cyt c concentration) was corrected by subtracting the background reading at 570 nm. The cyt c concentration was calculated by interpolating these values on a standard curve constructed for each plate. The above experiment was repeated five times.

Measurement of the ADP:ATP Ratio

After exposure of spermatozoa (1×10⁶/ml) to various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h, the measurement of the ADP:ATP ratio in spermatozoa was carried out by using an EnzyLight™ ADP/ATP Ratio Assay Kit (BioAssay Systems, USA) according to manufacturer’s instructions. Briefly, 10 µl of the washed spermatozoa (10³–10⁴) was transferred into a tube. 90 µl ATP Reagent was added to the tube and vortexed for 30 s. After 1 min, luminescence (RLU A) was recorded. Ten min later reading was repeated (RLU B). This measurement provided background prior to measuring ADP (i.e. the residual ATP signal). Immediately following reading RLU B, 5 µl ADP reagent was added to the tube and vortexed. After 1 min, luminescence (RLU C) was obtained. ADP/ATP Ratio = RLU C – RLU B/RLUA. All samples were performed in triplicate. The data from the ATP/ADP assay is presented as an average of the ATP/ADP ratios. The above experiment was repeated five times.

Assessment of Sperm Motility Parameters

After exposure of spermatozoa (2×10⁶/ml) to various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h, the MOT, HA, velocities (VSL, VCL, VAP) and other characteristics including CON, PMOT, STR, LIN, ALH and BCF were measured by using the Computer-Assisted Sperm Analyzer (Hamilton-Thorn Research, Danvers, MA, USA) at 37°C. The Burkman (1991) criteria for HA were used as follows: VCL≥100 um/s, LIN≤65% and amplitude of lateral head displacement (ALH)≥7.5 µm. Motility was defined as the percentage of sperm with VAP>7.5 µm/s. Sperm concentration was adjusted to ∼20×10⁶/ml by centrifugation at 700×g for 5 min and resuspended in 100 µl of the same medium. A sample of 5 µl was placed in a microcell (18.7 µm depth) for assessment of motility and velocities. For each sperm sample, an average of six (five to seven) fields with a total of 300–400 sperms was assessed.

Sperm- ZP Binding Test

Sperm-ZP binding test was performed as described previously [28]. Briefly, after exposure of spermatozoa (2×10⁶/ml) to various concentrations of HBs (0, 25, 50, 100 µg/ml) for 3 h, motile sperms of each group were incubated with four oocytes in a humidified incubator (37°C, 5% CO₂ in air) for 2 h, and then transferred to PBS containing 2 mg/ml bovine serum albumin (BSA, Sigma Chemicals Co., St. Louis, MO). The oocytes were flushed several times to dislodge loosely adherent sperm using a fine pipette approximately twice the diameter of the oocyte. The number of sperms bound to each of four oocytes was counted using an inverted phase contrast microscope and the average number of sperms bound per ZP was used as endpoint. Oocytes with>100 sperms bound were recorded as 100 since it is impossible to count the number accurately. In the present study, the above experiment was repeated five times and the average number of sperms bound to ZP in each group is expressed as median and quartile deviation per ZP.

Assessment of the AR of Sperms Bound to the ZP

Assessment of the AR of sperms bound to the ZP was performed as described previously [28]. Briefly, after counting the number of sperms bound to the ZP, all sperms bound to the surface of the four ZPs were removed by repeated vigorous aspiration with a narrow gauge pipette with an inner diameter of about 120 mm. This was performed on a glass slide with ∼5 µl PBS containing 0.2% BSA and dislodged sperms were smeared in a limited area (∼16 mm²), which was marked on the back of the slides with a glass pen to help find the sperm under the microscope for assessment of the AR. The AR of dislodged ZP-bound sperm was assessed using Pisum sativum agglutinin (PSA) conjugated with fluorescein isothiocyanate (Sigma Chemical Company, St Louise, MO, USA) as described previously [38]. After air-drying, sperm smears were fixed in 95% ethanol for 30 min and then stained using 25 µg/ml PSA in PBS for 2 h at 4°C. The slides were washed and mounted with distilled water and 200 sperms per sample were counted with a fluorescence microscope using excitation wavelengths of 450–490 nm and a magnification of 400 x. When more than half the head of a sperm was brightly and uniformly fluorescent, the acrosome was considered intact. Sperm with a fluorescent band at the equatorial segment or without fluorescence (a rare pattern) were considered acrosome reacted.

Statistical Analysis

The data are representatives of average of five independent experiments using sperm sample from five different men. The average values of data are expressed as mean ± SD. SPSS 17.0 programs were used in the statistical analysis. A paired t test was performed to evaluate the impact of HBs exposure. The number of sperms bound to ZP in each group is expressed as median and quartile deviation. A Kruskal-Wallis test in GraphPad Prism 5 was conducted to evaluate the differences among various concentrations of HBs (0, 25, 50, 100 µg/ml) on median change in number of sperms bound to ZP. P-value <0.05 was considered to be significant.