Cumulus-enclosed sheep oocytes were cultured in gonadotrophin-containing medium for up to 9 hr and were then incubated for 3 hr in the presence of [32P]phosphate. The incorporation of 32P into TCA-insoluble material was measured, and oocyte proteins were separated by one-and twodimensional gel elect
Nuclear decondensation of mammalian spermatozoa: Changes during maturation and in vitro storage
β Scribed by Beil, Richard E. ;Graves, Charles N.
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 700 KB
- Volume
- 202
- Category
- Article
- ISSN
- 0022-104X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Swelling of the spermatozoan nucleus and decondensation of the chromatin occur soon after penetration of spermatozoa into the egg cytoplasm. This decondensation was duplicated in vitro by incubating preβejaculatory ram, rabbit and bovine spermatozoa and also stored postβejaculatory bovine spermatozoa in 1% sodium dodecyl sulfate and 2.0 mM dithiothreitol. Spermatozoa obtained from the testis and epididymal caput, corpus and cauda showed a progressive resistance to nuclear decondensation, while no change was evident in the decondensation time of spermatozoa obtained from the epididymal cauda, vas deferens and ejaculated semen. There was also a significant increase in decondensation time after the spermatozoa had been stored in vitro at 25Β°C. This increased resistance to nuclear decondensation in the in vitro stored spermatozoa, reflecting an increase in crossβlinking within the spermatozoan histones by formation of disulfide bonds, may account for part of the increased embryonic mortality observed when spermatozoa are stored in vitro prior to insemination.
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