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Biological Research

versión impresa ISSN 0716-9760

Biol. Res. vol.44 no.4 Santiago  2011 

Biol Res 44: 329-337, 2011

Research Articles

Porcine oviduct sperm binding glycoprotein and its deleterious effect on sperm: a mechanism for negative selection of sperm?


Juan M. Teijeiro1, Dora G. Dapino2 and Patricia E. Marini1,3*

1 Instituto de Biología Molecular y Celular de Rosario (IBR-CONICET) y Área Biología, Facultad de Ciencias Bioquímicas y Farmacéuticas. UNR.

2 Cátedra de Fisiología. Facultad de Ciencias Veterinarias. UNR.

3 Member of the research career (CIC-UNR).


In their journey through the oviduct some subpopulations of sperm are preserved in a reservoir, while others are negatively selected. Sperm binding glycoprotein (SBG) is a pig oviductal epithelial cell glycoprotein that produces, under capacitating conditions, acrosome alteration, p97 tyrosine-phosphorylation and reduction of the motility of sperm. In this paper, we show that SBG is accessible at the extracellular surface of the oviductal epithelial cells, supporting a sperm interaction biological role in situ. We analyze the possible dependence of the tyrosine-phosphorylation of p97 on the PKA mechanism, finding that apparently it is not PKA dependent. Also, after SBG treatment the phosphorylated proteins locate mainly at the detached periacrosomal region and at the tail of sperm; the latter may be related to SBG's motility reduction effect. The study of the time course effect of SBG on sperm as detected by chlortetracycline (CTC) staining and of its binding to sperm by immunodetection in conjunction with CTC, shows results in agreement with the hypothesis that this glycoprotein is involved in the alteration of acrosomes in a specific sperm subpopulation. The results suggest that SBG may be part of a mechanism for negative selection of sperm.

Key words: acrosome alteration, tyrosine-phosphorylation.



The oviduct is a dynamic organ in which final gamete maturation takes place. The interaction between sperm and the oviduct results in a mechanism by which a subpopulation of sperm is stored forming a sperm reservoir. The formation of a sperm reservoir is a widespread process that ensures the availability of a suitable number of viable spermatozoa for fertilization (Tienthai et al., 2004) and has been shown for a variety of mammals including sheep (Hunter and Nichol, 1983), mice (Suárez, 1987; Kan and Esperanzate, 2006), hamsters (Smith and Yanagimachi, 1991; Kan and Esperanzate, 2006), cows (Hunter et al., 1991; Kan and Esperanzate, 2006), rats (Orihuela et al., 1999) and pigs (Hunter, 1981). This process includes spermatozoa binding to oviductal epithelial cells via the plasma membrane overlying the acrosome (Gualtieri and Talevi, 2000) in a carbohydrate recognition dependent way (DeMott et al., 1995; Lefebvre et al., 1997; Suárez, 2001; Wagner et al., 2002). The sperm proteins that have been assigned a function in sperm reservoir formation are spermadhesins DQH (Manaskova et al., 2007) and AQN1 (Ekhlasi-Hundrieser et al., 2005) in pig; and PDC109 (BSPA1/A2), BSPA3, and BSP30K in bull (Gwathmey et al., 2006). The oviductal proteins that have been related to this process are annexins A1, 2, 4 and 5 in cow (Ignotz et al., 2007) and annexin A2 in pig (Teijeiro et al., 2009). It is known that adhesion of sperm to form a reservoir occurs only for selected subpopulations that include sperm with intact acrosomes in cow (Gualtieri and Talevi, 2000); at an uncapacitated status for horse (Thomas et al., 1994), cow (Lefebvre and Suarez, 1996) and pig (Fazeli et al., 1999); with low internal free calcium content and reduced membrane protein phosphorylation for pigs and bovines (Petrunkina et al., 2001; Gualtieri et al., 2005); of superior morphology for horse (Thomas et al., 1994); and with normal chromatin structure for human and pig (Ellington et al., 1999; Ardón et al., 2008). Spermatozoa selected through oviductal adhesion have superior zona pellucida binding and fertilization ability (Gualtieri and Talevi, 2003). Detachment from the oviduct has been linked to protein loss upon capacitation (Topfer-Petersen et al., 2008), to hyperactivated motility (De Mott and Suárez, 1992; Pacey et al., 1995) and to protein disulfide reduction (Gualtieri et al., 2009). However, this would be only one of the forms of sperm-oviduct interaction as, in vivo, an apparent negative selection of sperm seems to occur in this organ. This selection remains a poorly studied event, but sperm subpopulations with altered plasma membranes have been detected in the lumen of the oviduct (Mburu et al., 1997; Tienthai et al., 2004). Interestingly, porcine sperm binding glycoprotein (SBG), which produces an acrosomal alteration effect on sperm incubated under capacitating conditions (Teijeiro et al., 2008), localizes to the apical surface of cells at the lumen of the oviduct, as determined by immunohistochemistry (Pérez et al., 2006). SBG was first isolated due to its capacity of association to sperm periacrosomal membranes; it shows an apparent molecular mass higher than 220 kDa and exposes Galp1-3GalNAc (Marini and Cabada, 2003). SBG produces alteration of pig sperm acrosome integrity, suppression of motility and tyrosine phosphorylation of a 97 kDa protein on spermatozoa (p97) (Teijeiro et al., 2008). These data lead us to propose that SBG is involved in sperm negative selection, producing its deleterious effect on sperm that suffer the capacitation process while being in the oviduct (Teijeiro et al., 2008). In this work we aim to advance on the characterization of SBG's location, effect and mechanism of action.



Unless otherwise stated, chemicals were obtained from Sigma-Aldrich (Argentina).

Semen collection and treatments

Semen was collected from adult boars of proven fertility and routinely used for artificial insemination (AI) by the glove-hand method. Sperm rich fraction was diluted in Cronos (Laboratorio Medi Chimica, Reggio Emilia, Italy), and conserved at 16°C until use (no more than 24 hours from collection). Quality of the samples was established by evaluating motility, viability, concentration, acrosomal and morphological parameters (Althouse, 1997).

Spermatozoa were recovered by centrifugation at 700 g for 5 minutes and washed twice in Tyrode's capacitating medium, TALP (Parrish et al., 1988), which contains 96 mM NaCl, 3.1 mM KCl, 2.0 mM CaCl2, 0.4 mM MgSO44 0.3 mM NaH2PO44 20 mM HEPES, 21.6 mM sodium lactate, 1 mM sodium pyruvate, 15 mM NaHCO3, 5 mM glucose, 285-315 mOsm. The sperm were resuspended to give a final concentration of 107 sperm/ml in the same medium.

SBG purification

SBG was purified as reported by Marini and Cabada (2003). Briefly, oviducts of gilts were obtained at a local abattoir and transported to the laboratory in ice-cold PBS. The isthmic section was separated and opened longitudinally. Epithelial cells were obtained by scraping with the blunt side of a scalpel blade, disaggregated, washed and disrupted in Potter homogenizer. Fractions enriched in plasma membrane were prepared by differential centrifugation. Extracts of these fractions were obtained by incubation in 0.5 M NaCl - 0.2% Triton X100 - 10 mM Tris-HCl pH 7.5 for 1 h at 4°C. After centrifugation at 105,000 g for 1 h at 4°C, the supernatants were dialyzed against TALP and used for affinity chromatography.

The affinity chromatography column was prepared by coupling of a fraction of boar sperm enriched in components from the periacrosomal and acrosomal external membranes to Sepharose CL4B (Marini and Cabada, 2003). Oviductal cell membrane extracts prepared as indicated above were applied and, after washing, elution was achieved with 0.5 M NaCl - 10 mM Tris-HCl pH 7.5. Only one protein peak was found on the bound fraction by measure of Absorbance at 280 nm. Purification of the native form of SBG was confirmed by SDS-PAGE on 5-12% polyacrylamide gradient gels according to Laemmli (1970); followed by silver staining (Rabilloud, et al. 1994).

In situ biotinylation of oviductal lumen

The biotinylation protocol was based on the method described by Holt et al. (2005). Batches of ten oviducts were trimmed from reproductive tissues and washed in ice-cold PBS. The isthmus section of each oviduct was separated, flushed with 2 ml of ice-cold PBS/CM (PBS containing 1.3 mM CaCl2 and 1 mM MgCl2, pH 7.2) and then with 2 ml of biotinylating reagent EZ-Link® Sulfo-NHS-SS-Biotin (Pierce, Thermo Scientific, USA) at 0.5 mg/ml in PBS/CM. The isthmic sections were clamped at each end, filled with the same solution and incubated 30 min at room temperature. After incubation, isthmus sections were emptied and the excess of biotin was inactivated by flushing with quenching solution (Pierce, Thermo Scientific, USA). One isthmus section of each batch was fixed in 4% formaldehyde and then processed to detect biotinylated proteins on tissue sections. In brief, tissue was dehydrated, embedded in paraffin, cut into 5 ìm sections, and mounted on slides optimized for immunohistochemistry (Frosted HiFixNH, TNT, Argentina). The other oviduct sections were opened longitudinally and epithelia were scraped with the blunt side of a scalpel blade and transferred to a 50 ml conical tube. Scraped cells were rinsed three times with 5 ml of TBS (25 mM Tris-HCl, pH 7.4, 150 mM NaCl) by centrifugation at 500 g for 3 min at 4°C. After rinsing, scraped cells were resuspended in lysis buffer (Pierce, Thermo Scientific, USA) and sonicated at 1.5%, five 1-second bursts. Cells were incubated 30 min on ice, vortexing every 5 min for 5 sec and then centrifuged at 10,000 g for 2 minutes at 4°C. Biotinylated proteins were purified by affinity to NeutrAvidinTM Agarose (Pierce, Thermo Scientific, USA) according to manufacturer's instructions.

Detection of biotinylated proteins and SBG on nitrocellulose membranes

Purified biotinylated proteins were separated in 5-12% SDS-PAGE and transferred to nitrocellulose membranes (GE Healthcare, Argentina) using Miniprotean 3 System (Bio-Rad, Hercules, CA). For biotinylated proteins detection, blots were incubated with ^g/ml peroxidase-conjugated streptavidin. For SBG detection, nitrocellulose membranes were incubated with 1:1000 anti-SBG (Pérez et al., 2006) and then with the second antibody (anti-rabbit IgG-horseradish peroxidase, GE Healthcare, UK) 1:10,000 v/v in TBS. In both cases labeled proteins were revealed using enhanced chemiluminescence detection with ECL Kit (GE Healthcare, Argentina) according to manufacturer's instructions. An aliquot of purified biotinylated proteins was resolved by 5-12% SDS-PAGE and visualized by silver staining.

Detection of biotinylated proteins on tissue sections

Tissue sections were deparaffinized in xylene, then rehydrated through graded dilutions of ethanol (100%, 95%, 70%, and 35%), followed by two washes in PBS. Endogenous peroxidases were inactivated by incubating slides for 30 min in 3% H2O2 in methanol, followed by three 5-min washes in PBS. Slides were incubated 1 h with 10 ìg/ml peroxidase-conjugated streptavidin and peroxidase activity was visualized by development with 3,3'-diaminobenzidine tetrahychloride (DAB).

Evaluation of the effect of SBG on sperm by CTC staining

Sperm were suspended in TALP supplemented with the indicated amounts of SBG (0, 100 ìg/ml, 150 ìg/ml) and with fetuin as specificity control. This protein was chosen because it does not contain Galp1-3GalNAc, the disaccharide exposed by SBG, which could be at least partially responsible for its biological effect. The concentrations of SBG used were based on studies of Berger et al. (1989) and Melendrez et al. (1994), for solubilized ZP as acrosomal inducers and previous work by us (Teijeiro et al., 2008) at lower concentrations (up to 50 ìg/ml give similar results, unpublished data). Samples were incubated at 37°C in a 5% CO2 atmosphere. At the times stated in each case an aliquot of sperm was examined by CTC staining as described by Dapino et al. (2006). In brief, CTC (750 ìM) was prepared in 20 mM Tris buffer containing 130 mM NaCl and 5 mM DL-cysteine (final pH 7.8). Sperm suspensions (5ì!) were mixed with 5 ì! of CTC solution on a warmed slide (37° C). After 30 sec, 5 ìl of 0.2% glutaraldehyde in 0.5 M Tris pH 7.4, were added. Finally, 5ìl of 0.22 M 1, 4-diaza-byciclo (2.2.2) octane (DABCO) in 50% glycerol were added to retard fluorescence fading. After adding a coverslip, slides were gently compressed using a tissue paper. The slides were then sealed along the edges with colorless nail varnish and examined with a microscope equipped with epifluorescence (Olympus BH2 Company Ltd., Tokyo, Japan). At least 100 cells were counted. Sperm viability was analyzed by eosin-nigrosin staining method and was at least of 75% after 1 h of incubation, which are the rates usually found for pig sperm.

Detection of SBG binding sites on sperm stained with CTC

Sperm were incubated in TALP in the presence of 150 ìg/ml of SBG for 1 h at 37°C. Five microlitres of sperm suspensions were mixed with 5 ìl of CTC solution on slides, then 5 ìl of 0.2% glutaraldehyde in 0.5 M Tris pH 7.4 were added and slides were air dried in darkness. The slides were gently rinsed with PBS twice, blocked with 2% bovine serum albumin - 0.2% Triton X100 in PBS for 60 min and then treated with the primary antibodies overnight at 4°C. Antibodies were polyclonal anti-SBG (1:50) (Pérez et al., 2006). After being rinsed twice with PBS, the slides were treated with Cy3 conjugated anti-rabbit immunoglobulin (Chemicon International, Inc. USA) (1:750) for 60 min. After rinsing twice with PBS, the slides were covered with 0.22 M DABCO dissolved in 50% glycerol and cover slips. Alternatively, sperm suspensions were incubated 1 h with 150 ìg/ml of SBG, then 30 min with polyclonal anti-SBG antibodies (1:50), air dried and then incubated 1 h with Cy3 conjugated anti-rabbit immunoglobulin (Chemicon International, Inc. USA) (1:750). After incubation, 5 ìl of sperm suspension were mixed with 5 ìl of CTC solution on slides, fixed and coverslip mounted with 5ìl of 0.22 M DABCO in 50% glycerol. For both protocols, slides were examined with microscope equipped with epifluorescence, counting at least 100 cells.

Detection and localization of phosphotyrosine containing polypeptides

Sperm suspensions were incubated for 1 hour at 37°C in a 5% CO2 atmosphere in TALP, and one aliquot was then treated with 10 ìM calcium ionophore A23187. Additionally, a sample was incubated for 30 min in TALP supplemented with 50 ìM of H89 PKA inhibitor and then 1 h with SBG at a final concentration of 150 ìg/ml. Another aliquot was incubated in TALP containing 150 ìg/ml of SBG. Cells (1 x 106 sperm) from each treatment were used for protein separation on 12% SDS-PAGE and proteins transferred to nitrocellulose membranes. Transferred proteins were visualized in the membrane by Pounceau S staining. Nonspecific binding sites were blocked by incubation with 5% dry non-fat milk in TBS. Membranes were treated with anti-phosphotyrosine monoclonal antibodies (clone 4G10, Upstate, Lake Placid, NY, USA) 1:2000 in TTBS (TBS plus 0.5% Tween 20) overnight at 4°C. After washing

(three times for 10 min each), the blot was incubated with peroxidase-conjugated goat anti-mouse antibodies at 1:2000 in TTBS for 120 min and washed again. Labeled proteins were revealed using enhanced chemiluminescence detection with ECL Kit (GE Healthcare, Argentina) according to manufacturer's instructions.

Aliquots of 5 ìl of sperm incubated with SBG, in TALP or non-incubated were smeared on slides, fixed with glutaraldehyde and air dried. Sperm were permeabilized by 30 min incubation in methanol, except when indicated. After blocking non-specific binding sites with 5% dry non-fat milk in TBS the slides were incubated with anti-phosphotyrosine monoclonal antibodies (1:100) overnight at 4°C. The primary antibodies were revealed with goat anti-mouse Alexa Fluor® 488-conjugated IgG (Invitrogen, Argentina) at 1:100 dilution. At least 100 cells were observed using an epifluorescence microscope.

Statistical analysis

The normality assumptions of data were studied by skewness and Kurtosis coefficients, normality plot and Wilk-Shapiro test. Percentages of spermatozoa with altered acrosomes (AA) and capacitated were subjected to two-way analysis of variance (ANOVA). When F-test results were significant in ANOVA, individual means were further tested by Tukey's multiple range test (Motulsky, 1995).


Accessibility of SBG at the extracellular surface of oviductal epithelial cells

An experimental strategy for studying surface-exposed proteins involved in porcine sperm-oviduct contact interactions was validated by Holt et al. (2005). This strategy was used to verify whether SBG is exposed on the surface of oviductal cells. The localization of this glycoprotein at the extracellular surface of isthmic epithelial cells would be an indication of its possible role. Using this strategy, superficial isthmic proteins were labeled with biotin in situ, and purified by affinity chromatography. Western blotting was performed on purified biotinylated proteins with anti-SBG antibodies. SBG was detected among the biotin-labeled purified proteins (Fig. 1A). Histochemistry of the in situ biotinylated proteins, as a control for possible intracellular biotinylation, confirmed the absence of biotinylated proteins in the cytoplasm of the cells (Fig. 1B and D). Immunolocalization of SBG in order to compare the localization of biotinylated protein and the localization of SBG is shown (Fig. 1C).

Effect of SBG over sperm as determined by Chortetracycline staining (CTC)

We have previously reported SBG induced acrosome alteration (AA) after 1 h of incubation of sperm under capacitating conditions detected by Wells and Awa staining (Teijeiro et al., 2008). This technique does not provide information about the capacitated sperm subpopulation. In order to obtain information about capacitated sperm, here we analyzed the effect of SBG by measuring the (CTC) patterns obtained at different times during 1 h of incubation. CTC staining allows the detection of sperm at initial steps of capacitation Interestingly, when SBG was present in the media, not only the patterns usually found (Wang et al., 1995) for intact (pattern F, Fig. 2A) acrosome-reacted (pattern AR, Fig. 2B) and capacitated sperm (pattern B, Fig. 2C) were seen, but also new patterns appeared in which the acrosome seems to be altered (Fig. 2D and E) and which are compatible with the images previously detected by Wells and Awa staining (Teijeiro et al., 2008). In these patterns, the detached periacrosomal membrane (Fig. 2D, bracket) or swelling (Fig. 2E, arrow) figures seen at the acrosomal region show fluorescence. Sperm showing these patterns were counted together with sperm showing pattern AR, which represented 4-7% sperm in every condition tested, to determine the rate of AA sperm.

When the time course effect was analyzed by CTC staining, at 40 min of incubation in capacitating conditions AA augmented slightly and to a same amount for 100 ìg/ ml of SBG and for fetuin, used as a specificity control (see Material and Methods). A greater increase was seen for sperm incubated in the presence of 150 ìg/ml SBG (Fig. 3A). At this time, a significant increase in pattern B (capacitated) of CTC staining was also noted for control sperm (Fig. 3B). After 1 h of incubation both concentrations of SBG produced a significant augment of AA with respect to the control, at a rate similar to the one previously detected by Wells and Awa staining (Teijeiro et al., 2008), the effect of 150 ìg/ml of glycoprotein being greater than that of 100 ìg/ml (Fig. 3A). At this time, however, the rate of pattern B (capacitated), augmented only for the fetuin containing control, reached 21.6%. Surprisingly, when SBG was present, the rate of capacitated sperm did not vary throughout the whole experiment for 100 ìg/ml of SBG, being the same of non-incubated samples. For 150 ìg/ ml of glycoprotein, the rate of pattern B (capacitated) sperm diminished significantly after 1 hour of incubation, becoming lower than in capacitating medium without SBG (Fig. 3B). However, at least 3% pattern B sperm were detected at every time point in every condition used.

Immunolocalization of SBG on CTC stained sperm

In order to analyze the physiological state of sperm bound to SBG, the glycoprotein was detected by immunochemistry using anti-SBG specific antibodies on CTC-stained sperm after 1 h of incubation under capacitating conditions in the presence of 150 ì g/ml of SBG. Alternatively, SBG detection was performed previous to CTC staining. The results obtained with both protocols were indistinguishable.

Most sperm (more than 79%) presented a CTC pattern compatible with AA. All these sperm showed patches of SBG over the periacrosomal region by immunochemistry analysis (Fig. 4C and D). The rest of the sperm could be classified in two categories: the typical CTC pattern B (3.3%), corresponding to capacitated sperm that did not exhibit bound SBG in any case; and CTC pattern F, compatible with unmodified sperm (10.1% of total sperm) (Fig. 4A), which showed SBG bound to the whole periacrosomal region (Fig. 4B).

The effect of SBG on p97 tyrosine-phosphorylation

SBG enhances the tyrosine-phosphorylation of a protein of apparent molecular mass 97 kDa (p97) (Teijeiro et al., 2008). As the cAMP-dependent protein kinase A (PKA) has been associated with sperm capacitation, motility and acrosome reaction, we hypothesized that this protein may be related to the mechanism of p97 tyrosine-phosphorylation by effect of SBG. To test this possibility, sperm were incubated in the presence of 150 ìg/ml SBG in TALP capacitating medium with and without prior treatment with the PKA inhibitor H89. As controls, sperm incubated in capacitating conditions in the absence of SBG and incubated in capacitating conditions followed by acrosome reaction induction with calcium ionophore A23187 were used. As shown in figure 5, H89 (50 ìM) did not affect p97 tyrosine-phosphorylation by SBG. Another concentration of H89 (100 ìM) was also tested, giving the same result (data not shown). The controls of capacitated and acrosome reaction induced sperm did not show p97 tyrosine-phosphorylation, and exhibited characteristic patterns, including the induction of p32 tyrosine-phosphorylation in capacitated sperm (Fig. 5) (Dubé et al., 2005). Sperm in which acrosome reaction was induced by calcium ionophore did not show phosphorylated p32.

Cellular distribution of tyrosine-phosphorylated proteins upon SBG treatment

The localization of tyrosine-phosphorylated proteins on sperm was determined by immunocytochemistry. Non-incubated sperm showed signal mainly in the equatorial region (Fig. 6A) and sperm incubated in capacitating conditions showed the presence of tyrosine-phosphorylated proteins only in the acrosomal and equatorial regions (Fig. 6B). When sperm were incubated in the presence of 150 ìg/ml SBG in capacitating conditions, tyrosine-phosphorylated proteins localized to the fragments of the altered or detached acrosomal membrane, and, in a small portion of the population to the flagellum (Fig. 6C). When the detection of tyrosine-phosphorylated proteins on SBG treated sperm was conducted without permeabilization, staining was limited to the periacrosomal detached fragments (Fig. 6C, inset). Controls without primary antibody showed no significant fluorescence (not shown).


SBG's localization in the regions of the oviduct surrounding the lumen and at the apical membrane of epithelial cells is a main consideration regarding its function. To be able to interact with sperm in their journey through this organ the glycoprotein should be accessible to sperm at the extracellular surface of the cells. Our previous results showing SBG's localization by immunohistochemistry (Pérez et al., 2006) did not deal with this task. The detection of SBG by a validated strategy for studying porcine oviductal surface-exposed protein (Fig. 1) establishes that the glycoprotein is accessible at the extracellular surface of the oviductal epithelial cells, where it may contact with sperm in vivo, supporting a possible role on sperm-oviduct interaction.

We have previously reported results concerning SBG's effect on acrosome alteration on sperm only when they are incubated in capacitating conditions. These results were based on observations made by Wells and Awa staining, that distinguishes between acrosome reacted and not reacted sperm, after progesterone stimulus. That is to say, only sperm in conditions to undergo acrosome reaction are counted as capacitated. However, capacitation is a complex process that involves many metabolic and membrane associated changes, giving as a final result sperm in conditions as to undergo acrosome reaction. A variety of techniques allow the detection of changes associated with capacitation, among them CTC staining (Wang et al., 1995) shows increased membrane fluidity that occurs early in the process, well before sperm are able to proceed to acrosome reaction (Tardiff et al., 1999). In order to establish if SBG acts only over fully capacitated sperm or also on sperm in the first stages of capacitation, in this work, we analyze SBG's time course effect on sperm by CTC staining. It is interesting to note that SBG treated sperm show patterns in which the periacrosomal membrane seems to be detached or swelled, and yet are fluorescent (Fig. 2), in accordance with the morphology first found after SBG treatment by Wells and Awa staining (Teijeiro et al., 2008). This AA associated sperm resemble the pattern LCP described for human, which was proposed to represent partial acrosome-reacted sperm (Perry et al., 1995).

The AA effect of SBG is first detected, for the higher concentration, concomitant with an augment of pattern B (capacitated) sperm in the control (Fig. 3), suggesting that as soon as sperm begin the capacitating process, SBG may produce its effect. The slight increase of AA sperm in the control observed from this time on, may be due to spontaneous acrosome reaction of capacitated sperm, and is also seen for the lowest SBG concentration, which may be too low to produce noticeable AA effect after 40 minutes of incubation. This response is generally attributed to a degenerative process of sperm that are fully capacitated (Dapino et al., 2006). After one hour of treatment, AA was detected showing an SBG concentration dependent effect and in amounts comparable to those observed using Wells and Awa staining (Teijeiro et al., 2008), while the control showed the expected rate of pattern B (capacitated) and AA sperm.

Interestingly, pattern B sperm did not increase in time in SBG treated samples (Fig. 3). Also, the presence of SBG could not be detected bound to pattern B sperm (Fig. 4), but was observed on every pattern F (intact) sperm after one hour of incubation. Taken together, these results support the hypothesis that among the sperm population there is always a small amount of sperm (at least 3%) that are refractory to SBG binding, and also a certain amount of sperm in the appropriate physiological state as to begin capacitation. When the appropriated subpopulation of sperm begins the capacitation process, at least in vitro, the presence of SBG produces AA. These would leave a small amount of CTC pattern B sperm at any time, which are probably unable of interacting with SBG. The decrease of pattern B (capacitated) found for 150 ìg/ml of SBG after 1 hour of incubation, when AA sperm constitute almost 80% of the population, may be due to a diminution of sperm in the appropriate physiological state as to begin the capacitation process. In vivo, at pre- and peri-ovulatory stages of the porcine oestrus, only 1-5% sperm undergo capacitation in the oviduct, while a significant increase (14%) of capacitated sperm is found in this organ at post-ovulatory oestrus (Tienthai et al., 2004). This difference has been related to changes in the oviductal fluid composition (Tienthai et al., 2004). Thus, in pre-ovulatory oestrus, interaction between oviductal SBG and sperm wouldn't cause any effect, as the gametes are immersed in a non-capacitating environment, and at the post-ovulatory stages, when capacitation is promoted by the oviductal milieu, SBG would produce AA of the remaining sperm. Considering that, at least in pig, polyspermy is thought to originate principally from increased numbers of capacitated spermatozoa reaching the site of fertilization (Hunter, 1972; Hunter, 1976; Hunter et al., 1991); that the isthmus limits the passage of spermatozoa to the upper regions of the Fallopian tubes in vivo (Hunter and Leglise, 1971; Hunter, 1973); and that sperm with acrosomal alteration or acrosome-reacted cannot bind to ZP, excluding them for the fertilization race (Fazeli et al., 1997), the possible reduction of the number of sperm reaching the ampulla in capacitated state due to SBG's effect, could be considered, in certain manner, as a pre-fertilization polyspermy prevention mechanism in vivo.

When immunodetection of SBG was done over CTC stained sperm the glycoprotein was detected on patches on AA (and LCP-like) pattern and in pattern F, confirming that it remains bound after producing its effect (Fig. 4D). Thus, sperm that suffer AA due to interaction with SBG in the lumen of the isthmus at post-ovulatory stages of oestrus would keep SBG bound at their altered acrosomal membrane. Considering that ZP3a (Mr 55 kDa) binds to the acrosome region of acrosome-damaged or partially acrosome-reacted spermatozoa (Yonezawa et al., 2005), that Mr 55 kDa zona pellucida component exhibits Galp1-3GalNac, as does SBG (Marini and Cabada, 2003), and that deglycosylation of Mr 55 kDa makes ZP unable to trigger acrosomal reaction, it is possible that SBG bound to AA sperm would block their interaction with ZP3a. Reduction of the number of sperm bound to the zona may serve to reduce the incidence of polyspermy (Hunter, 1993; Killian, 2004). Thus, this could constitute another indirect pre-fertilization mechanism of polyspermy prevention by SBG, similar to what was demonstrated for oviductal-specific glycoprotein, at least in vitro (Kouba et al., 2000). This mechanism would require SBG to be ripped from the oviductal epithelium upon sperm liberation, which is plausible, given that it can be easily extracted in vitro (Marini and Cabada, 2003). Another interesting study shows that SBG is resistant to trypsin and chemotrypsin degradation (Marini and Cabada, 2003); such property would make the glycoprotein resistant to in situ degradation by enzymes liberated from the acrosome upon AA, allowing it to protect the epithelium from enzymatic damage.

It is generally accepted that sperm capacitation, motility and acrosome reaction are associated with protein kinase-A-mediated tyrosine phosphorylation of proteins (Urner and Sakkas, 2003). In boar sperm, however, the appearance of phosphorylated p32 is considered related to capacitation (Tardif et al., 2001), but its phosphorylation is independent of the cAMP/PKA pathway (Tardif et al., 2004). We have previously reported the induction of tyrosine-phosphorylation of p97 by SBG in boar sperm incubated under capacitating conditions. In this work we show that p97's phosphorylation induction by SBG is apparently also independent of PKA, as it is not affected by the inhibitor H89 (Fig. 5), which does not affect p32 phosphorylation during capacitation either (Fig. 5) (Tardif et al., 2004). Thus, an alternative mechanism seems to mediate SBG signal transduction in boar sperm, as also happens for p32 tyrosine-phosphorylation (Tardif et al., 2004). SBG produces tyrosine-phosphorylation of proteins located at the flagellum of pig sperm, and tyrosine-phosphorylation of proteins of the periacrosomal membranes that seem to remain in the attached altered periacrosomal membranes (Fig. 5). Only the last is seen when tyrosine-phosphorylated proteins are detected without permeabilization of sperm, indicating that only the periacrosomal proteins are exposed. Phosphorylated p32 is liberated/dephosphorylated from sperm upon acrosome alteration (Fig. 5-6), as well as in ionophore-induced acrosome reaction (Fig. 5). Tyrosine-phosphorylation of proteins located in the head of sperm (Fig. 6B) is characteristic of the capacitated state (Dubé et al., 2005). The phosphorylation of flagellar proteins under capacitating conditions has been shown for several mammals in association to hyperactivated motility (Mahony and Gwathney, 1999; Nassar et al., 1999; Si and Okuno, 1999) but, to the best of our knowledge, not for pigs. Further studies are needed to identify p97 and elucidate its possible mechanism of action. However, as SBG diminishes the motility of sperm (Teijeiro et al., 2008), the tyrosine-phosphorylation of proteins located in the tail it promotes, seems to have the opposite effect of that reported for other mammals. Interestingly, suppression of motility produced by proteins derived from oviductal epithelial cells plasma membranes, has been considered as part of a sperm selection mechanism (Satake et al., 2006). In conclusion, we have previously proposed that SBG may interact with sperm that have begun capacitation when they arrive to the oviduct and produce acrosome rupture or, alternatively, it may be involved in sperm attachment to the oviduct and produce alteration of acrosomes in a sperm-subpopulation specific manner that may involve calcium and bicarbonate microenvironment availability (Teijeiro et al., 2008). The evidence presented in this work supports the later hypothesis. Furthermore, a possible mechanism of negative selection by SBG is suggested, based on this further analysis of its action.


We thank Veterinarian Fernando Cane for kindly providing the sperm samples and Frigorífico Paladini SA for the oviducts. This work was supported in part by UNR, and the ANPCyT-BID program PICT 1284 of Argentina.


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* Corresponding author: Patricia E. Marini, Facultad de Ciencias Bioquímicas y Farmacéuticas, Suipacha 531 - S2002LRK - Rosario, Argentina. Tel.: 0054 341 4350661 ext 122 -Fax: 0054 341 4804601. e-mail: -

Received: November 29, 2010. In revised form: January 11, 2011. Accepted: March 21, 2011.

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