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Biology of Reproduction, Vol 13, 304-313, Copyright © 1975 by Society for the Study of Reproduction
1 Departments of Animal Science
Pathology and Biochemistry
University of Florida
Gainesville, Florida 32610 A fluorescent antibody technique was used to study the site of synthesis, movement and steroid
control of porcine purple acid phosphatase uterine protein in uterine and oviducal tissues on Days
0, 3, 6, 9, 12, 15 and 18 of the estrous cycle. Uterine, oviduct and placental tissues were obtained
from pregnant gilts on Days 9, 15, 18, 20, 30, 50, 70 and 90 of gestation. In addition, uterine
tissue was obtained from ovariectomized animals subjected to various steroid hormone treatments.
The oviducal epithelium and uterine surface and glandular epithelium showed various degrees of
fluorescence at different stages of the estrous cycle with an apparent change in pattern coincidental
with fluctuations in ovarian steroid levels. It was concluded that estrogen may be required for
initiation of synthesis of this protein, but progesterone induced full synthesis and secretory
activity. Enzyme assays performed on uterine flushings from each day of the estrous cycle support
the immunofluorescent results. In pregnant gilts, oviducal and uterine surface and glandular
epithelium showed fluorescence at all stages of gestation studied. A significant difference was
observed in the pattern of fluorescence between uterine endometrium of early pregnancy and that
of the corresponding stages of estrous cycle. As pregnancy progressed, placental areolae became
strongly fluorescent, indicating absorption of uterine gland secretions by these structures.
Inhibition of uterine secretory activity took place in association with rising estrogen levels toward
the end of gestation. This study suggests that the purple acid phosphatase is synthesized and
secreted by the uterine epithelial cells under the influence of progesterone and that placental
areolae serve as sites of absorption and transport of this protein across the chorio-allantoic
membranes and into the allantoic fluid where it is sequestered during pregnancy.
Accepted on June 6, 1975
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