## Abstract Preincubation of sperm in medium for three hours before mixing with ova increased the number of ova fertilized after one hour, thus indicating that sperm maturation occurs in vitro. The presence of cumulus cells increased the proportion of ova fertilized as observed at two and at three
Maturation and sperm penetration of canine ovarian oocytes in vitro
β Scribed by Mahi, Cherrie Ann ;Yanagimachi, Ryuzo
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 537 KB
- Volume
- 196
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Canine ovarian oocytes were cultured in a medium consisting of TC medium 199, fetal calf serum and antibiotics. Ninetyβnine percent of the apparently healthy oocytes were in the germinal vesicle (dictyate) stage when recovered from the ovaries; 25% of them reached metaphase I or II by 72 hours of culture. Washed ejaculated spermatozoa were added to BWW medium containing oocytes which had either been removed directly from the follicles or which had been cultured for 24β72 hours. The earliest acrosome reaction and zona penetration by spermatozoa were seen at seven hours after insemination. Seventyβfour percent of the oocytes examined between 11 and 24 hours after insemination showed evidence of zona penetration by spermatozoa. Neither the condition of the oocyte vitellus nor the stage of nuclear maturation influenced the incidence of zona penetration. Decondensing sperm nuclei were found in the vitellus of 27% of the oocytes which had not been cultured and in the vitellus of 20% of those which had been cultured for 24β72 hours and were in various stages of maturation. These results indicate that (1) canine ovarian oocytes can be matured in vitro, (2) the spermatozoa require capacitation which takes approximately seven hours in vitro and (3) maturation of the oocytes is not required for sperm passage through the zona pellucida or entry into the vitellus nor for sperm nuclear decondensation.
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## Abstract (C57BL/10 Γ CBA)F~1~ mouse eggs were incubated in vitro with either F~1~ or outbred TO sperm for 15 minutesβ6 hours. Upon removal from the sperm suspensions some eggs were treated with pronase to remove zonae and then cultured, while the remainder were simply cultured to allow a compari
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