Abstract
This study compared the in vitro development of Day-2 equine embryos co-cultured with either trophoblastic vesicles or oviductal explants. Embryos were collected surgically from the oviducts of pony mares 2 d after ovulation and assessed for stage of development. Culture medium was Ham's F12 and Dulbecco's Modified Eagle's Medium (50:50 v/v) in a humidified atmosphere of 5% CO2 in air at 38.5° C with either trophoblastic vesicles or oviductal explants. The quality score of embryos was assessed daily. After 4 d in culture, embryos were stained (Hoechst 33342) and evaluated with epifluorescence to determine the number of nuclei present. Six of seven embryos co-cultured with oviductal exmplants developed to the morula/blastocyst stage, while four of seven embryos co-cultured with trophoblastic vesicles developed to the morula stage. More (P = 0.1) embryos co-cultured with oviductal explants reached the blastocyst stage than embryos co-cultured with trophoblastic vesicles ( 3 7 vs 0 7, respectively). The number of cells was higher (P = 0.1) for embryos co-cultured with oviductal explants than for embryos co-cultured with trophoblastic vesicles (162.6 ± 32 vs 87.3 ± 28, respectively). The number of cells for embryos co-cultured with either oviductal explants or trophoblastic vesicles appeared to be lower than for embryos matured in vivo that were recovered from the uterus at Day 6 (378, 399, >1000). The co-culture of early equine embryos in a completely defined medium with either trophoblastic vesicles or oviductal explants can support development to at least the morula stage. The co-culture of embryos with oviductal explants resulted in superior development of four-to eight-cell embryos, as indicated by the proportion that reached the blastocyst stage and by the number of cells.
Original language | English |
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Pages (from-to) | 669-682 |
Number of pages | 14 |
Journal | Theriogenology |
Volume | 35 |
Issue number | 3 |
DOIs | |
State | Published - Mar 1991 |
Bibliographical note
Funding Information:Acknowledgments We thank the Travers Thoroughbred Research Fund and Thornbrook Farms for financial support. We thank Dr. R. H. Foote for the use of laboratory facilities used in staining embryos. Technical assistance was provided by S. Bartlett, P. Luddy, M. McCann and J. St. Leger. We also thank C. Collyer and the staff of the Equine Research Park for animal care. A portion of these results has been presented previously (1).
Keywords
- co-culture
- embryo
- equine
- oviduct
- trophoblastic vesicle
ASJC Scopus subject areas
- Small Animals
- Food Animals
- Animal Science and Zoology
- Equine