Jk. Thibodeaux et al., STIMULATION OF PROGESTERONE PRODUCTION IN BOVINE LUTEAL CELLS BY COINCUBATION WITH BOVINE BLASTOCYST-STAGE EMBRYOS OR TROPHOBLASTIC VESICLES, Journal of Reproduction and Fertility, 101(3), 1994, pp. 657-662
A study was conducted to determine whether bovine blastocyst-stage emb
ryos and trophoblastic vesicles stimulate the production of progestero
ne in bovine luteal cells during incubation in vitro. The effects of c
o-incubation of these embryos and vesicles with uterine endometrial ti
ssue on progesterone production was also investigated. Bovine small an
d large luteal cells were obtained on day 12 of the oestrous cycle, di
spersed by unit gravity sedimentation and recombined to provide prepar
ations free of accessory cells. Blastocyst-stage embryos were obtained
on day 7 and trophoblastic vesicles were obtained from bovine embryos
on day 12. A uterine endometrial tissue sample was obtained from the
same cow from which the corpus luteum was taken. Treatment groups were
arranged in 24-well plates as follows: luteal cells alone; luteal cel
ls and one trophoblastic vesicle; luteal cells and one blastocyst embr
yo; luteal cells and a 10 mg uterine endometrial sample; luteal cells,
one trophoblastic vesicle and a uterine endometrial sample; and lutea
l cells, one blastocyst embryo and a uterine endometrial sample. All t
reatment groups were incubated (at 37 degrees C under 5% CO2) in Ham's
F-12 medium supplemented with antibiotics (100 mu g penicillin ml(-1)
and 100 U streptomycin ml(-1), L-glutamine (0.29 mg ml(-1)), insulin
(5 mu g ml(-1)), transferrin (5 mu g ml(-1)) and selenium (5 ng ml(-1)
) for 12 h. Samples of the medium were harvested 10 min (basal concent
ration) and 2, 6 and 12 h after incubation to determine the concentrat
ions of progesterone and prostaglandin. The major findings of this stu
dy were that both trophoblastic vesicles and blastocyst-stage embryos
stimulated progesterone production during the 12 h incubation. In addi
tion, the uterine endometrial sample partially inhibited the stimulato
ry actions of trophoblastic vesicles and blastocyst embryos after 12 h
of incubation.