Cholesterol efflux from bovine sperm: II. Effect of reducing sperm cholesterol on penetration of zona-free hamster and in vitro matured bovine ova
- 1 August 1988
- journal article
- research article
- Published by Wiley in Gamete Research
- Vol. 20 (4) , 413-420
- https://doi.org/10.1002/mrd.1120200403
Abstract
Several reports have indicated that sperm capacitation includes loss of membrane cholesterol (Chol) with a concomitant decrease in the Chol-to-phospholipid (PL) ratio. Methods were developed for quantifiable removal of bovine sperm Chol, which predisposed sperm to induction of the acrosome reaction upon addition of lysophosphatidylcholine (LPC). The objective of this study was to evaluate the effect of Chol removal from bovine sperm on penetration of zona-free hamster and intact bovine ova in vitro. Washed ejaculated bovine sperm were incubated (2 h, 39°C) in a modified Tyrode's solution (TALP) containing (1) Chol-free liposomes (—Chol, 50 × 106 sperm and 600 nmol phospholipid/ml); (2) liposomes containing 30 mol% Chol (+ Chol, 2 × 108 sperm and 300 nmol total lipid/ml); or (3) no liposomes (Control). We have previously shown that net Chol efflux from sperm is 31% of the total sperm Chol with —Chol liposomes and less than 1% with control media. Sperm were then washed twice and challenged with LPC bound to bovine serum albumin (BSA) using celite as a carrier. Treated sperm (25 × 106) were incubated immediately with either zona-free hamster ova (HO) or in vitro matured bovine ova (BO) in 50-μl droplets of TALP under medical fluid in an atmosphere of 5% CO2 in air (3 h, 39°C). Ova were fixed in ethanol:acetic acid, stained with 1% orcein, and examined. Percent penetration (%P) of HO (X ± SEM) for 30 and 40 μg of LPC/mg BSA was 59.4 ± 5.3 and 82.9 ± 5.4; 38.5 ± 5.6 and 52.3 ± 4.7; and 16.0 ± 4.6; and 23.2 ± 5.6 for —Chol, Control, and + Chol treatments, respectively (n = 3). %P of BO (X ± SEM) for 30, 35, and 40 μg of LPC/mg BSA was 43.3 ± 5.4, 70.7 ± 7.5, and 81.5 ± 5.1 for —Chol and 16.4 ± 6.9, 36.2 ± 6.9, and 44.2 ± 8.6 for Control treatments, respectively (n = 3). In a second set of experiments %P of BO (X ± SEM) was 63.6 ± 6.8, 31.8 ± 4.9, and 10.5 ± 3.4 for —Chol, Control, and +Chol treatments, respectively, when 40 μg LPC/mg BSA was added (n = 2). %P and the number of sperm per fertilized ovum were consistently higher for the —Chol treatment for both HO and BO (P < .01). These results demonstrate that Chol removal from bovine sperm facilitates penetration of ova in vitro suggesting a potential role in bovine sperm capacitation.Keywords
This publication has 17 references indexed in Scilit:
- Human sperm nuclei can transform into condensed chromosomes in Xenopus egg extractsGamete Research, 1988
- Homospermic versus heterospermic insemination of zona‐free hamster eggs to assess fertility of fluorochrome‐labeled acrosome‐reacted bull spermatozoaGamete Research, 1987
- Reversible Inhibition of Rabbit Sperm- Fertilizing Ability by Cholesterol Sulfate1Biology of Reproduction, 1987
- Effect of Dilauroylphosphatidylcholine on the Acrosome Reaction and Subsequent Penetration of Bull Spermatozoa into Zona-Free Hamster EggsBiology of Reproduction, 1986
- Cholesterol and the cell membraneBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1985
- Albumin-Mediated Changes in Sperm Sterol Content During Capacitation 1Biology of Reproduction, 1985
- Factors Affecting Successful in Vitro Fertilization of Bovine Follicular OocytesBiology of Reproduction, 1983
- Timing of fertilization in mammals: sperm cholesterol/phospholipid ratio as a determinant of the capacitation interval.Proceedings of the National Academy of Sciences, 1981
- Interaction of phosphatidylcholine with bovine serum albumin. Specificity and properties of the complexesBiochimica et Biophysica Acta (BBA) - Protein Structure, 1976
- DECAPACITATION AND RECAPACITATION OF RABBIT SPERMATOZOA TREATED WITH MEMBRANE VESICLES FROM SEMINAL PLASMAReproduction, 1974