The effect of semen extension, cAMP and caffeine on in vitro fertilization of bovine oocytes.

A previously reported in vitro system that used epididymal spermatozoa for fertilizing bovine follicular oocytes (1) has been expanded to include ejaculated semen as the sperm source. Frequency of fertilization was higher when semen was extended 1:1 prior to transport to the laboratory rather than transport as neat semen. Pretreatment of spermatozoa with cAMP, caffeine or both prior to insemination of oocytes did not increase frequency of either acrosome reactions or fertilization after sperm/oocyte incubation.

Fertilizability of in vitro matured oocytes from golden hamsters.

The fertilizability of hamster oocytes matured in vitro was examined along with two factors potentially affecting nuclear maturation in culture. The four amino acids (isoleucine, methionine, phenylalanine, and glutamine) necessary for nuclear maturation of cumulus-free oocytes (Gwatkin and Haidri, '74) were not required if oocytes recovered on the morning of proestrus (day 4) were cultured with intact cumuli. Although follicular oocytes recovered on day 3 of the estrous cycle (late diestrus) had somewhat lower frequencies of maturation in vitro compared to those recovered on day 4 (76 vs. 95%, respectively), they still had a substantial frequency of spontaneous maturation. Follicular oocytes recovered on day 3 and matured in vitro were fertilized at frequencies equivalent to oviducal oocytes (80 vs. 82%, respectively) when incubation of oocytes with precapacitated sperm was continued for 6 h. Penetration of follicular oocytes was lower (37.4%) after only 4 h of sperm/egg incubation, indicating a delay in sperm penetration with follicular oocytes matured in vitro. Incubation for 4 h is sufficient time for penetration of 80% or more of oviducal oocytes. While 98% of penetrated oviducal oocytes were fertilized normally, only 2% of penetrated follicular oocytes were normal. The majority (85%) of follicular oocytes, unlike oviducal oocytes, were unable to cause decondensation of sperm nuclei after 6 h of sperm/egg incubation. Use of a highly defined system for in vitro fertilization of hamster gametes has provided rigorous proof that isolated cumulus-oocyte complexes do not undergo complete maturation in vitro.

Preovulatory changes in cumulus-oocyte complex of the hamster.

An orderly series of associations was found between the cumulus and the stages of nuclear development in the hamster oocyte as the oocyte-cumulus complex underwent preovulatory maturation. Ten hours prior to ovulation meiotic resumption was first seen in the oocyte. The onset of cumulus dissociation with corresponding morphological changes in cumulus cells was observed eight hours prior to ovulation. Completion of the first meiotic division in the oocyte and full cumulus dissociation occurred 2 hours prior to ovulation. Cumulus dissociation was found to occur only in vesicular follicles destined to ovulate and not in follicles undergoing atresia. Cells with large vacuolar inclusions with distorted, hyperchromatic nuclei were found in the maturing cumulus.

Effects of epinephrine and hypotaurine on in-vitro fertilization in the golden hamster.

Using an experimental design in which the addition of hypotaurine or epinephrine was staggered through time, evidence was found that suggests these two compounds are working independently and sequentially to stimulate the fertilizing capacity of hamster spermatozoa in vitro. Prior exposure of spermatozoa to hypotaurine is a prerequisite for the action of epinephrine in causing activation and penetration of hamster ova. A definite role for hypotaurine in inducing capacitation of hamster spermatozoa is also demonstrated. The alpha-adrenergic antagonist, phentolamine, was more effective in blocking fertilization of hamster ova in vitro than was propranolol, a beta-antagonist. This indicates tha catecholamines may be working by way of alpha-adrenergic receptors in causing capacitation of hamster spermatozoa. The failure to block fertilization with phentolamine after epinephrine has exerted its effect implies that epinephrine acts in a hormone-like fashion.

Development of preimplantation embryos of the golden hamster in a defined culture medium.

Eight-cell embryos were recovered from mated golden hamsters that had been superovulated with pregnant mare's serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG). Embryos were cultured for 24 or 32 h in a defined medium (modified Tyrode's solution) designed for fertilization of hamster oocytes in vitro. This medium was supplemented in some experiments with amino acids (glutamine, phenylalanine, methionine and isoleucine) and with vitamins (Eagle's Minimum Essential Medium vitamin supplement). At the end of the culture period, the numbers of embryos developing to the blastocyst stage were recorded. In other experiments, the effects of varying the osmotic pressure (225, 250, 275 and 300 m0smol/kg) and the pH (6.8 and 7.4) of the culture medium on blastocyst formation were examined. A difference was found between the ability of early 8-cell embryos (approx. 54 h post-egg activation) and late 8-cell embryos (approx. 62 h post-egg activation) to develop in culture. In the unsupplemented culture medium, only 2% of early 8-cell embryos developed to the blastocyst stage compared with 22% of late 8-cell embryos. A marked effect of the four amino acids on development was found. In the presence of amino acids 36% of early 8-cell embryos developed into blastocysts (18-fold increase). The amino acids also increased the percentage of late 8-cell embryos that developed into blastocysts from 22% to 66%. These data suggest that an important metabolic change may occur in hamster embryos during a critical period at the 8-cell stage of development. No additional effect on development was observed when vitamins were included in the culture medium. No significant effect of either osmotic pressure of pH of the culture medium on development was found. When blastocysts formed from cultured 8-cell embryos were transferred surgically to pseudopregnant hamsters, about 25% developed into normal-looking fetuses and 5 normal-looking young were born, 4 of which have survived. These results represent an approach towards achieving complete preimplantation development of hamster embryos in vitro.

Role of calcium and the calcium-calmodulin complex in resumption of meiosis, cumulus expansion, viability and hyaluronidase sensitivity of bovine cumulus-oocyte complexes.

The necessity of calcium (Ca2+) and the Ca2+-calmodulin complex for resumption and completion of meiosis, expansion of cumulus cells, viability and hyaluronidase sensitivity of in vitro cultured bovine cumulus-oocyte complexes was examined by inhibition of the Ca2+-calmodulin complex with eight graduated doses of trifluoperazine (TFP) and by Ca2+ deficiency or depletion. Doses of TFP greater than 2.5 microM decreased the percent of cumulus complexes surviving culture and oocytes completing meiosis, whereas cumulus expansion was unaffected until the cultures contained a near lethal dose (greater than 10 microM). Hyaluronidase caused dispersion of cumulus cells whenever they were expanded regardless of TFP dose. In TC-199 media the completion of meiosis I was suppressed by 0.1 to 1 mM ethylenediaminotetraacetic acid (EDTA) (P less than 0.05) and drastically reduced by 1.0 mM (P less than 0.05). Viability of the cumulus-oocyte complex was not reduced until the dose of EDTA was increased to 1.0 mM (P less than 0.0001). Cumulus expansion was also not suppressed until the dose of EDTA reached 1.0 mM (P less than 0.05). In Ca2+-free (CF) basal media Eagles, completion of meiosis I was reduced by all doses of EDTA (P less than 0.05), whereas viability of the cumulus-oocyte complex was decreased by Ca2+ deficiency or by EDTA addition to basal media Eagles (P less than 0.01). Cumulus expansion was unaffected by Ca2+ removal or chelation. In all experiments, oocytes which were not degenerate underwent germinal vesicle breakdown regardless of treatment.

Maturation and fertilization of bovine oocytes in vitro.

This report is to review and summarize various aspects of maturation and fertilization of bovine oocytes. Reference also is made to other species where pertinent data for the bovine are unavailable. Finally, factors important to success of in vitro maturation and fertilization as well as applications of these procedures to the animal industry are addressed.

In vitro maturation and fertilization of bovine oocytes are temperature-dependent processes.

Effects of temperature on bovine sperm acrosome reaction, oocyte maturation, hyaluronic acid production by cumulus cells and in vitro fertilization were studied. Viability and a true acrosome reaction of bovine spermatozoa were impaired at 40 degrees C. Temperatures lower than 35 degrees C did not enhance the acrosome reaction. However, viability between 30 degrees C-38 degrees C was not altered after 22 h of incubation. The optimal temperature for the acrosome reaction was 38 degrees C. Labeled glucosamine incorporation into glycosaminoglycans was not different among temperatures of 35 degrees C, 37 degrees C or 39 degrees C, whereas 41 degrees C caused a significant reduction (P less than 0.02). Temperatures ranging between 35 degrees C-39 degrees C had no deleterious effects on resumption and completion of meiosis, but at 41 degrees C the frequency of oocytes that progressed to Metaphase II was significantly reduced (P less than 0.0001). Ova matured at 39 degrees C had significantly higher rates of fertilization than at 35 degrees C, 37 degrees C, or 41 degrees C. Killed spermatozoa (control) had no effect on ovum activation at 39 degrees C. From these results it was concluded that events occurring prior to and during fertilization are temperature sensitive.

Factors affecting successful in vitro fertilization of bovine follicular oocytes.

These experiments were designed to define and optimize the efficiency of a system whereby bovine oocytes could be fertilized in vitro. The frequency of ova penetrated and the stage of fertilization were the end points examined. All experiments utilized cumulus-oocyte complexes from 1- to 5-mm follicles which were matured in vitro prior to fertilization. The experiments were designed to examine the effects of the following factors on fertilization: 1) pretreatment of sperm with ionomycin (a Ca++ ionophore), 2) preincubation of sperm at a high concentration and the presence of hypotaurine and epinephrine during fertilization, 3) the use of either follicle-stimulating hormone (FSH) or cAMP for the induction of cumulus expansion prior to fertilization, and 4) the need for the presence of cumulus cells during fertilization. Sperm exposure to ionomycin or preincubation at high sperm concentrations was not necessary for fertilization. The presence of hypotaurine and epinephrine during fertilization improved (P less than 0.05) the quality of fertilization (i.e., higher frequencies of oocytes with both female and male pronuclei were observed). However, they did not increase the percentage of ova penetrated (P greater than 0.05). Fertilization frequencies were not different (P greater than 0.05) between oocytes with cumulus expansion induced by FSH or cAMP. However, the use of either treatment resulted in higher fertilization rates when compared to untreated controls (P less than 0.05). Finally, while the presence of cumulus cells was not necessary for penetration of ova, increased frequencies of ova with both male and female pronuclei were found when cumuli were present (P less than 0.05).