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Effect of medium on the kinematics of frozen–thawed ram spermatozoa

Faculty of Veterinary Science, University of Sydney, New South Wales 2006, Australia

Correspondence should be addressed to S T Mortimer who is now at Oozoa Biomedical Inc., Box 93012 Caulfield Village RPO, West Vancouver, British Columbia V7W 3G4, Canada; Email: sharon{at}oozoa.com

	Abstract

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 
Cervically inseminated cryopreserved ram spermatozoa have reduced fertility due to poor mucus-penetrating ability. This effect is ameliorated by the addition of 20% (v/v) seminal plasma (SP) to the phosphate-buffered saline (PBS) thawing medium. The aims of this study were to determine whether the impaired mucus penetration was due to alterations in the sperm motility and, if so, whether these alterations were due to the SP or its viscosity, or to the medium components. To this end, artificial SP medium (ASP), a medium which supports motility but not capacitation, was compared with PBS and SP. Thawed, pooled semen from seven mature rams was layered under 1 ml each of PBS, SP and ASP and motile spermatozoa allowed to swim up (37 °C, 30 min). Upper regions of the overlays were harvested, and the capacitation status of the spermatozoa in each suspension determined by chlortetracycline (CTC) analysis. Sperm movement was videotaped in 300 µm chambers for both computer-aided sperm analysis assessment and manual flagellar curvature analysis. There was no effect of the culture medium on the concentration of spermatozoa recovered by swim up, nor on the proportion of motile spermatozoa. However, the spermatozoa resuspended in PBS did show changes associated with capacitation in both the CTC-binding patterns and in their movement patterns. These changes were significantly greater than those observed in spermatozoa resuspended in SP or ASP. These results indicated that the differences in sperm movement and function observed in SP medium were not due to changes in viscosity, but rather to components of the medium.

	Introduction

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 
It has been observed that cryopreservation of ram semen causes capacitation-like changes in the spermatozoa after thawing (Watson 1995). These spermatozoa have patterns of chlortetracycline (CTC) binding consistent with those seen in capacitated spermatozoa (Pérez et al. 1996), and do not require further incubation to acquire the ability to fertilize oocytes in vitro (Watson 1995). It has also been found that frozen–thawed spermatozoa resuspended in phosphate-buffered saline (PBS) are less able to penetrate cervical mucus in vitro than those resuspended in a mixture of seminal plasma (SP) and PBS (Maxwell et al. 1999). These results suggest that impairment of sperm transport through the cervix may be a contributing factor to the reduced fertility rates experienced for cervical insemination of frozen–thawed ram spermatozoa (Byrne et al. 2000), and also that the function of frozen–thawed spermatozoa could be affected by the medium used for resuspension.

Sperm transport through the cervix is a product of sperm movement and mucus quality. Only seminal spermatozoa with good, progressive motility and a high amplitude of lateral head displacement are able to penetrate oestrous cervical mucus (Aitken et al. 1985, Feneux et al. 1985, Mortimer et al. 1986). It is known that spermatozoa incubated under capacitating conditions, in the absence of SP, exhibit different movement patterns (kinematics) from seminal spermatozoa (which are the ones that penetrate cervical mucus in vivo) (reviewed by Mortimer, 1997). Therefore, it is possible that both the changes wrought by the freezing and thawing processes, as well as the absence of SP in prepared sperm populations, each act to inhibit sperm transport in the cervix and the upper female reproductive tract. This has major implications in the use of frozen–thawed semen for artificial insemination in sheep, since the tortuous nature of the cervical canal precludes intrauterine insemination by passage of a catheter through the cervix and requires that laparoscopic insemination be used.

In a recent study it was found that frozen–thawed ram spermatozoa resuspended in a solution of 20% (v/v) SP in PBS did not exhibit the same precocious capacitation, as measured by CTC binding, as those resuspended in PBS alone (Maxwell et al. 1999). It was further found that these spermatozoa gave significantly higher pregnancy rates following intracervical insemination compared with spermatozoa resuspended in PBS alone. This difference was attributed, at least in part, to the differences in sperm–mucus penetration, and hence sperm transport. However, the study did not consider whether sperm kinematics differed between the treatment groups.

If a difference in kinematics did exist between frozen–thawed spermatozoa resuspended in PBS alone and those resuspended in an SP/PBS solution, it would then be necessary to determine whether the difference was due to SP factor(s) or to the medium components. This could be done with a medium which did not promote capacitation, but which supported motility, such as the ‘artificial SP’ (ASP) medium developed by O’Donnell (1969) for use with bovine spermatozoa.

The aim of this study was to determine the effect of these different media on the kinematics of frozen–thawed ram spermatozoa, using CTC binding to confirm that the effect of SP supplementation was consistent with that reported previously (Maxwell et al. 1999).

	Materials and Methods

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Cryopreserved spermatozoa
Semen was collected from mature rams using an artificial vagina. Sperm concentration was assessed by haemocytometry and motility was assessed by wave motion (Evans & Maxwell 1987). Samples with a sperm concentration of 3.5–6 x 10⁹ and motility >75% were pooled, placed in a 30 °C water bath and diluted 1 + 4 with a temperature-equilibrated cryopreservation medium containing 300 mM Tris, 28 mM glucose, 95 mM citric acid, 15% (v/v) hen’s egg yolk and 5% (v/v) glycerol (Evans & Maxwell 1987). The diluted semen was cooled slowly to 5 °C over 2 h. Semen pellets were frozen by placing 200 µl droplets of the cooled diluted semen directly onto carbonic ice, then transferred to liquid nitrogen for storage. At thawing, three semen pellets were transferred into a dry glass tube and incubated at 37 °C with shaking. Volumes of 100 µl of the thawed semen were then layered under 1 ml culture medium in 5 ml plastic tissue culture tubes (Falcon no. 2057; Becton–Dickinson, Lane Cove, NSW, Australia), and the motile spermatozoa were allowed to swim up into the culture medium during an incubation period of 30 min at 37 °C. The upper regions of the overlays were harvested and pooled for each medium used, taking care not to contaminate the preparation with diluted semen. Preparations were maintained at 37 °C until use, 15 to 30 min later. Three pools of cryopreserved spermatozoa from a total of seven rams were used in this study.

Preparation of SP
Semen collected from mature rams by artificial vagina was pooled and centrifuged (3500 g, 15 min, 18 °C). The supernatant was harvested and mixed with Dulbecco’s PBS (Oxoid, Basingstoke, Hants, HAM, UK) to a final concentration of 20% (v/v) SP, then filtered through a 0.22 µm filter to remove any cellular debris. After filtration, 1 ml volumes of the preparation were stored at -20 °C until use.

Culture media
The control medium was PBS containing 10 mg/ml bovine serum albumin (BSA; fraction V, Sigma, Castle Hill, NSW, Australia). The ASP medium contained 38 mM sodium citrate, 10 mM sodium chloride, 50 mM potassium chloride, 1 mM sodium dihydrogen phosphate, 6 mM calcium chloride, 5 mM magnesium chloride and 30 mM fructose (O’Donnell, 1969), supplemented with 10 mg/ml BSA. The SP medium was the prepared 20% (v/v) pooled, cell-free ram SP in PBS, containing 3 mg/ml BSA. All media were temperature-equilibrated to 37 °C before use.

CTC analysis
The CTC staining solution contained 20 mM Tris, 130 mM NaCl, 5 mM cysteine and 750 µM CTC. The fix solution contained 1% (v/v) glutaraldehyde in a 1 M Tris–HCl buffer (pH 7.4). The mounting solution was 0.22 M 1,4-diaza-bicyclo[2.2.2] octane triethylenediamine (Sigma) in a 10% PBS/90% glycerol mixture (Gillan et al. 1997).

For staining, 45 µl volumes of sperm suspension were mixed with 45 µl CTC staining solution, before the addition of 10 µl fix solution. Then, 10 µl volumes of the stained sperm suspension were mixed with 5 µl mounting solution on microscope slides (two preparations were made for each sperm suspension) before a 22 x 22 mm coverslip was placed over each sample. The samples were compressed by application of firm but gentle pressure to each coverslip. The slides were then randomized and coded to allow ‘blinded’ scoring. Fluorescence was observed with an Olympus BX50 microscope using a 40 x objective and a DM-455 dichroic mirror, a BP-405 band pass filter and a Y-476 barrier filter. At least 200 spermatozoa were scored for each slide, and three fluorescent staining patterns were identified: ‘F’ pattern, bright post-acrosomal or entire head fluorescence; ‘B’ pattern, bright acrosome region fluorescence; and ‘AR’ pattern, no head fluorescence or fluorescence in the equatorial region only.

Videotaping sperm movement
For videotaping sperm movement, sperm preparations were loaded into prewarmed 300 µm deep chambers (Microslides; VitroCom Inc, Mountain Lakes, NJ, USA), and the ends sealed with Cristaseal haematocrit sealant (Cope Scientific, Newcastle, NSW, Australia). The loaded microslides were placed in a 37 °C incubator until sperm movement was videotaped. Sperm movement was visualized using an Olympus BH-S microscope with phase contrast optics, and recorded using a Sony NTSC video camera with a 1/250 s electronic shutter and a Sony SLV-EZ8 video cassette recorder (Sony Australia, North Ryde, NSW, Australia). For the videotapes which were to be analysed by CASA, a 10 x NH phase contrast objective was used, while a 40 x PL phase contrast objective was used for the higher magnification videotapes used for flagellar analysis. The same preparations were recorded using each set of optics, so the manual and CASA analyses were drawn from the same sperm populations. The final magnifications were derived from measurement of the intervals on a stage micrometer which was recorded at the beginning of each videotape. All analyses were performed at an image sampling frequency of 60 Hz.

Flagellar movement analysis
The 40 x PL recordings were used in the evaluation of flagellar movement. Spermatozoa were chosen for inclusion in the study based solely upon the clarity of the flagellar image, and lack of interaction (collisions) with other spermatozoa. There was no attempt to evaluate the quality of sperm movement before the flagellar traces were made.

The videotapes were replayed using a Panasonic AG-4700 video cassette recorder and a Panasonic video monitor (WV-CM2000; GEC Electronics, North Ryde, NSW, Australia) which gave a final on-screen magnification of 2900 x . The outline of the whole spermatozoon was traced directly from the monitor onto a sheet of overhead projector film, then the videotape was advanced one video field and the outline of the spermatozoon traced again. One quarter of a second of movement was reconstructed for each spermatozoon (15 images). The relative orientation of the spermatozoon during the sequence was controlled for by tracing a fixed crosshair onto each image in the sequence.

The flagellar curvature ratio (FCR) was determined for each spermatozoon traced (Fig. 1). FCR is defined as ‘the straight-line distance from the head/midpiece junction to the first inflection point of the tail, divided by the curvilinear distance between these two points as measured along the tail’ (Suarez et al. 1983). For each flagellar trace studied, the point of inflection was identified and the curvilinear distance determined by running a curvimeter along the proximal portion of the tail trace. The straight-line distance was measured using a millimetre rule.

View larger version (7K): [in this window] [in a new window]   Figure 1 Derivation of the FCR, which is the ratio of the straight-line distance to the curvilinear distance measured from the head/midpiece junction to the first inflection point of the sperm tail.

Statistics
² analyses were used to compare CTC results. The kinematic values were compared using unpaired Wilcoxon tests, and the influence of medium upon movement was determined using the Kruskal–Wallis test, analysis of variance and unpaired t-tests (MedCalc for Windows; Med-Calc Software, Mariakerke, Belgium).

	Results

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 
Sperm selection
There was no effect of culture medium on the concentration of spermatozoa recovered by swim up, with average recoveries of 28, 26 and 24 x 10⁶/ml for PBS, SP and ASP respectively. Similarly, there was no significant effect of culture medium on the proportion of motile spermatozoa recovered by swim up (88, 96 and 93% respectively; Ht = 1.1067, P = 0.578 by Kruskal–Wallis test).

Effect of medium on CTC staining patterns
The number of F-patterned spermatozoa was significantly higher in the ASP medium than in either SP or PBS (both P < 0.0001). Also, significantly more spermatozoa in the SP medium were F patterned than those in the PBS medium (P < 0.05). These differences in the proportions of F-patterned spermatozoa were accounted for by corresponding differences in the proportions of B-patterned spermatozoa, with no difference observed between the treatments upon the proportions of AR-patterned spermatozoa (Fig. 2).

View larger version (15K): [in this window] [in a new window]   Figure 2 Effect of medium on CTC patterns for spermatozoa resuspended in PBS, PBS supplemented with 20% (v/v) SP and ASP media. The CTC-binding patterns were uncapacitated (F pattern), capacitated (B pattern) and acrosome-reacted (AR) pattern. PBS gave the lowest proportion of ‘uncapacitated’ (F-patterned) spermatozoa, indicating significant membrane destabilization. Bars are the mean values ±2 S.E.M., approximating the 95% confidence intervals.

View larger version (13K): [in this window] [in a new window]   Figure 3 Effect of medium on FCR of spermatozoa resuspended in PBS, PBS supplemented with 20% (v/v) SP and ASP media. A total of 30 spermatozoa per medium were assessed, with the lowest value over 15 consecutive images taken as the FCR value for each. The spermatozoa resuspended in PBS had the lowest FCR values, meaning that they had the most acute proximal flagellar bends. The notches in the notched box-and-whisker plots for each medium did not overlap, indicating a significant difference between the medians at a ±95% confidence level.

View larger version (28K): [in this window] [in a new window]   Figure 4 Effect of medium on sperm kinematics VCL, VSL, VAP, LIN, STR, WOB, ALH, DNCmean, D and BCF. Bars are the mean values ±2 S.E.M., approximating the 95% confidence intervals of a total of 2099 trajectories assessed using computer-aided sperm analysis. Statistical significance was determined by Kruskal–Wallis comparisons of each trajectory’s kinematics. Spermatozoa resuspended in PBS medium had consistently different kinematics from those in SP or ASP.

	Discussion

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 
The problem of poor fertility rates following cervical insemination of frozen–thawed ram spermatozoa has been a vexatious issue for many years. The observation that the inclusion of SP in the thawing medium resulted in a consistent, significant improvement in pregnancy rates (Maxwell et al. 1999) indicated that factor(s) in the SP were responsible for this improvement, and therefore that the thawing medium itself (PBS) was in some way deficient. It was shown in that study that the presence of SP in the thawing medium reduced the proportion of spermatozoa with B pattern by CTC (indicating increased plasma membrane stabilization), and also increased the proportion of spermatozoa able to penetrate cervical mucus in vitro. Cervical mucus penetration has been related to sperm motility, and specifically to spermatozoa with good linear progression and moderate amplitudes of lateral head displacement (Aitken et al. 1985, Feneux et al. 1985, Mortimer et al. 1986). Therefore, it seems logical that observed differences in mucus-penetrating ability would be reflected in differences in sperm kinematics, as well as in differences in head plasma membrane stability.

The assessment of plasma membrane stability was included in the present study to confirm that the effect of SP supplementation of the PBS was similar to that previously reported (Maxwell et al. 1999). The relative proportions of F- and B-patterned spermatozoa indicated that the SP conferred a significant stabilizing effect, but also that the ASP medium had an even greater stabilizing effect giving significantly more F-patterned spermatozoa than either PBS or SP (Fig. 2). This effect was unexpected, given that the same protein supplementation was used for both PBS and ASP, so the only differences between the media were the salts used.

The spermatozoa used in this study were obtained by a direct swim up from the thawed semen pellets into each of three culture media, so only motile spermatozoa were selected. The similar recoveries of motile spermatozoa from the swim-up preparations indicated that there was no effect of the medium on sperm concentration or total motility, and therefore it is a reasonable assumption that similar sperm populations were recruited. However, there was a significant effect of the culture medium on flagellar movement, and therefore upon the kinematics. The flagellar analyses were performed manually, with no bias as to the individual spermatozoa studied. Spermatozoa resuspended in PBS had the most acute proximal flagellar curvature while those in ASP had the lowest degree of proximal flagellar bending (Fig. 3). Spermatozoa resuspended in the SP medium had intermediate levels of flagellar bending. Increased proximal flagellar curvature has been described as a feature of hyperactivated spermatozoa in capacitation medium (Mortimer et al. 1997), although the threshold FCR for hyperactivated ram spermatozoa has been reported to be 0.64 (Mortimer & Maxwell 1999), so while the spermatozoa in PBS were exhibiting an unusual flagellar beat pattern, it was not consistent with hyperactivated motility per se.

While observation of flagellar movement gives the most direct information regarding the effect of the culture medium upon motility, the relatively low number of cells which can be examined requires that supporting observations be made. The most convenient method for the analysis of large numbers of spermatozoa is CASA, in which each sperm head trajectory is reconstructed and its kinematics derived. For all of the kinematic values determined in this study, there were significant differences between those of the spermatozoa resuspended in PBS and those in SP or ASP (Fig. 4). The most obvious differences were for the fractal dimension and for DNCmean, which is defined as VCL/VSL x ALHmean (Robertson et al. 1988). DNCmean was developed as a marker for hyperactivated motility of human spermatozoa, with a threshold value of 17. This value was not reached for the ram spermatozoa, indicating that while the trajectories of spermatozoa in PBS were not linear, they were not hyperactivated.

The fractal dimension (D) was also significantly higher for spermatozoa in PBS than those in either SP or ASP. This kinematic value provides an indication of the complexity of the trajectory, increasing from D = 1.0 for a straight line. The mean D value for the spermatozoa resuspended in PBS was 1.38, while the mean D value for spermatozoa resuspended in either SP or ASP was 1.21 (Fig. 4). These results do not suggest that the spermatozoa in PBS were hyperactivated, but do indicate that their trajectories were significantly less linear than those of spermatozoa in SP or ASP.

The results of this study have suggested that the differences observed in the ability of spermatozoa resuspended in PBS and in SP to penetrate ovine cervical mucus in vitro (Maxwell et al. 1999) were due, at least in part, to alterations in sperm kinematics, rather than simply to the CTC status. Other studies of sperm–mucus interaction have shown that kinematics can be used to identify ‘mucus-penetrating’ spermatozoa in fresh semen and that this subpopulation of spermatozoa have good velocity and increased ALH (Aitken et al. 1985, Feneux et al. 1985, Mortimer et al. 1986). While the thawed ovine spermatozoa resuspended in PBS did have these characteristics, it would seem that their trajectories were not sufficiently linear, and hence too complex, to allow good mucus penetration. Uncapacitated mammalian spermatozoa have a flagellar beat pattern characterized by relatively long wavelength, low amplitude waves, consistent with resistance to bending provided by the fibrous sheath. This pattern is similar to that observed for spermatozoa resuspended in SP and in ASP in this study. However, as capacitation progresses, the flagellar bends occur more proximally and are more acute, suggesting that this type of movement, as seen in the spermatozoa resuspended in PBS, is associated physiologically with transport in the upper, rather than the lower, female reproductive tract.

In conclusion, it appears that while the thawed ram spermatozoa did, indeed, show many signs of capacitation, these changes could be ameliorated by altering the medium in which they were cultured after thawing. Further studies of ASP are warranted to determine its applicability as a thawing medium for spermatozoa to be used in the cervical insemination of ewes.

	Acknowledgements

Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 
This work was supported by a U2000 post-doctoral fellowship grant and a University Research Grant from the University of Sydney.

	Footnotes

 
Received 7 May 2003
First decision 30 June 2003
Revised manuscript received 6 October 2003
Accepted 16 October 2003

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Top Abstract Introduction Materials and Methods Results Discussion Acknowledgements References

 

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