Biosynthesis and Degradation of Canine Placental Prostaglandins: Prepartum Changes in Expression and Function of Prostaglandin F2alpha-Synthase (PGFS, AKR1C3) and 15-Hydroxyprostaglandin Dehydrogenase (HPGD)1
Authors:
- Aykut GramAykut Gram
- Urs BüchlerUBUrs Büchler
- Alois BoosABAlois Boos
- Bernd HoffmannBHBernd Hoffmann
- Mariusz P. KowalewskiMariusz P. Kowalewski
- 1 July 2013
- journal article
- Published by Oxford University Press (OUP) in Biology of Reproduction
- Vol. 89 (1) , 2
Abstract
There is no distinct explanation of the mechanism for the prepartal prostaglandin F2alpha (PGF2alpha) increase in pregnant dogs. Although the PGF2alpha-synthase (PGFS [AKR1C3]) mRNA expression and localization profiles have been previously investigated in canine utero/placental compartments, the availability and biochemical activity of the PGFS (AKR1C3) protein remain unknown. In order to better understand the regulation of canine uterine PGF2alpha availability and eventual prepartum release in luteolytic amounts in dogs, canine-specific PGFS (AKR1C3) and 15-hydroxyprostaglandin dehydrogenase (HPGD) antibodies were generated and used to characterize the expression, cellular localization, and biochemical properties of PGFS (AKR1C3) and HPGD in the utero/placental compartments and corpus luteum throughout pregnancy and at prepartum luteolysis. PGFS (AKR1C3) expression was weak or absent in luteal samples. Uterine PGFS (AKR1C3) was up-regulated postimplantation and declined prepartum. The utero/placental expression of PGFS (AKR1C3) was identified in the superficial uterine glands throughout gestation and in the trophoblast cells within the feto-maternal contact zone during placentation, suggesting a possible role for PGFS (AKR1C3) in the trophoblast invasion. Utero-placental HPGD was up-regulated until postimplantation, lower at midgestation, and greatly suppressed at prepartum. Expression was routinely identified in the endometrial surface and glandular epithelia, and positive signals were also observed in the trophoblast cells at the feto-maternal contact zone. The biochemical activity of recombinant PGFS (AKR1C3) and HPGD was confirmed after its expression in a heterologous system. The colocalization of HPGD with PGFS (AKR1C3) expression suggests a modulatory role for HPGD as a gatekeeper of the supply of prostaglandin in the pregnant canine uterus.Keywords
This publication has 17 references indexed in Scilit:
- Canine prostaglandin F2α receptor (FP) and prostaglandin F2α synthase (PGFS): Molecular cloning and expression in the corpus luteumAnimal Reproduction Science, 2008
- Characterization of the canine 3β-hydroxysteroid dehydrogenase and its expression in the corpus luteum during diestrusThe Journal of Steroid Biochemistry and Molecular Biology, 2006
- Expression of cyclooxygenase 1 and 2 in the canine corpus luteum during diestrusTheriogenology, 2006
- In vitro PGF2α production by endometrium and corpus luteum explants from pregnant and nonpregnant diestrus bitches and placental explants from pregnant bitchesTheriogenology, 2006
- Regulation of Corpus Luteum‐function in the BitchReproduction in Domestic Animals, 2004
- Prostaglandin Metabolism in the Ovine Corpus Luteum: Catabolism of Prostaglandin F2α (PGF2α) Coincides with Resistance of the Corpus Luteum to PGF2α1Biology of Reproduction, 2000
- The enzymes responsible for the metabolism of prostaglandins in bovine placentaProstaglandins, Leukotrienes and Essential Fatty Acids, 1999
- Cloning and expression of the cDNA for mouse NAD+-dependent 15-hydroxyprostaglandin dehydrogenaseBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1996
- Prostaglandin-Metabolizing Enzymes During Pregnancy: Characterization of NAD+-Dependent Prostaglandin Dehydrogenase, Carbonyl Reductase, and Cytochrome P450-Dependent Prostaglandin Omega-HydroxylaseCritical Reviews in Biochemistry and Molecular Biology, 1996
- Investigations on hormonal changes around parturition in the dog and the occurrence of pregnancy-specific non conjugated oestrogensExperimental and Clinical Endocrinology & Diabetes, 1994