The effect of altering uterine space available to developing conceptuses on placental and endometrial protein secretion and endometrial 3H-thymidine incorporation on Days 25 and 35 of gestation was tested. Gilts bred at estrus (Day 0) were laparotomized on Day 4, and the uterine horn ipsilateral to the ovary with the most ovulations was ligated midway between the uterine tip and uterine bifurcation to create a crowded and a roomy uterine environment. On Day 25 (n = 7) or 35 (n = 6), gilts were killed and the reproductive tract was dissected from each. Each placenta and fetus was weighed, and a sample of endometrium adjacent to each placenta was collected. Within each uterine environment, tissues (500 mg) from the heaviest and lightest (by weight) placentae and adjacent endometrial tissue were cultured for 24 h at 37 degrees C in 15 ml Minimal Essential Medium having 0.1 times the normal amount of leucine plus 50 microCi 3H-leucine. Aliquots (2 ml) of dialyzed medium were subjected to two-dimensional PAGE and fluorography to examine proteins with molecular weight ranges of approximately M(r) 20,000-130,000, and a further aliquot was subjected to SDS-PAGE to examine low molecular weight proteins (M(r) 2000-20,000). In addition, endometrium (200 mg in duplicate) adjacent to the heaviest and lightest placentae within each uterine environment was incubated for 4 h in 5 ml MEM plus 1 microCi 3H-thymidine to measure DNA synthesis. After culture, 3H-thymidine incorporation and total DNA were determined. Fetal survival in the crowded uterine environment decreased (p < 0.05) on Day 35 compared to Day 25. On both days, the heaviest and lightest placentae from the crowded uterine environment weighed less (p < 0.01) than the heaviest and lightest placentae from the roomy uterine environment. The fetuses associated with the heaviest and lightest placentae from the crowded uterine environment also weighed less (p < 0.05) than fetuses associated with the heaviest and lightest placentae from the roomy uterine environment. Nondialyzable radioactivity in medium per gram of tissue cultured from placental cultures decreased (p < 0.05) and from endometrial culture increased (p < 0.05) between Days 25 and 35. Placental secretion of a protein with M(r) 46,000, pI 5, decreased between Days 25 and 35. Endometrial secretion of three proteins (M(r) 35,000, pI 6.2; M(r) 25,000, pI 4.9; and M(r) 14,000, pI unknown) increased, and secretion of three other proteins (M(r) 24,000, pI 6.5 doublet; M(r) 22,000, pI 7.5, and M(r) 7000, pI unknown) decreased from Day 25 to Day 35 of pregnancy.(ABSTRACT TRUNCATED AT 400 WORDS)
[1]
R. Hunter.
Fertilization in the Pig and Horse
,
1991
.
[2]
Z. Y. Chen,et al.
Effect of initial length of uterus per embryo on fetal survival and development in the pig.
,
1989,
Journal of animal science.
[3]
G. L. Bennett,et al.
Integration of ovulation rate, potential embryonic viability and uterine capacity into a model of litter size in swine.
,
1989,
Journal of animal science.
[4]
D. Stringfellow,et al.
Mitogenic activity in ovine uterine fluids: characterization of a growth factor activity which specifically stimulates myoblast proliferation.
,
1988,
Biochemical and biophysical research communications.
[5]
R. Roberts,et al.
The effect of ovine trophoblast protein-one on endometrial protein secretion and cyclic nucleotides.
,
1987,
Biology of reproduction.
[6]
H. Schägger,et al.
Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa.
,
1987,
Analytical biochemistry.
[7]
R. Christenson,et al.
Justification of unilateral hysterectomy-ovariectomy as a model to evaluate uterine capacity in swine.
,
1987,
Journal of animal science.
[8]
R. Kittok,et al.
Selection for components of reproduction in swine
,
1984
.
[9]
K. Paigen,et al.
A simple, rapid, and sensitive DNA assay procedure.
,
1980,
Analytical biochemistry.
[10]
R. Roberts,et al.
The secretion of a uterine specific, purple phosphatase by cultured explants of porcine endometrium: dependency upon the state of pregnancy of the donor animal.
,
1979,
Biology of reproduction.
[11]
G. J. King,et al.
Plasma concentrations of progesterone, oestrone, oestradiol-17beta and of oestrone sulphate in the pig at implantation, during pregnancy and at parturition.
,
1974,
Journal of reproduction and fertility.
[12]
B. N. Day,et al.
Synchronization of estrus and ovulation in superovulated gilts.
,
1973,
Journal of animal science.
[13]
C. Polge,et al.
Time of cessation of intrauterine migration of pig embryos.
,
1970,
Journal of animal science.
[14]
B. N. Day,et al.
Fertility level of sows superovulated at post-weaning estrus.
,
1968,
Journal of animal science.
[15]
J. S. Perry.
The incidence of embryonic mortality as a characteristic of the individual sow.
,
1960,
Journal of reproduction and fertility.
[16]
C. Brambel.
Allantochorionic differentiations of the pig studied morphologically and histochemically
,
1933
.