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Unité dOntogénie & Reproduction, Centre de Recherche du Centre Hospitalier de lUniversité Laval, Ste-Foy, Québec, Canada G1V 4G2; and Centre de Recherche en Biologie de la Reproduction and Département dObstétrique et Gynécologie, Université Laval, Ste-Foy, Québec, Canada GIV 4G2
Address all correspondence and requests for reprints to: Dr. Michel A. Fortier, Ph.D., Unité DOntogénie & Reproduction, Bloc T1-49, Centre de Recherche du CHUL, 2705 Boulevard Laurier, Ste-Foy, Québec, Canada G1V 4G2. E-mail: mafortier{at}crchul.ulaval.ca.
Uteroplacental prostaglandins (PGs) play pivotal roles in maintenance and /or termination of pregnancy in mammals. Regulation of PG biosynthetic and signaling mechanisms in uteroplacental tissues during maintenance of pregnancy is largely unknown. In the present study, we have characterized the expression of PGE2 receptors (EP2, EP3, EP4), PGF2
receptor (FP), and cyclooxygenase (COX) types 1 and 2 in placentome caruncle (CAR), intercaruncle, and fetal membrane tissues during pregnancy in cattle. Pregnant bovine uteri were collected and classified into six groups covering the entire gestational length. The levels of expression of EP2, EP3, and FP mRNAs differ depending on tissues and days of gestation (days < 50 to > 250). EP4 mRNA was undetectable in all the tissues studied. The expression levels of PG receptor mRNAs were as follows: placentome CAR FP > EP2 >EP3, intercaruncle EP2 > EP3
FP, and fetal membranes EP3
EP2 >> FP. EP2 and EP3 expressions were modulated in uteroplacental tissues, depending on days of pregnancy, whereas FP was uniformly expressed. COX-1 mRNA and protein were constitutively expressed, whereas COX-2 was highly modulated in uteroplacental tissues throughout pregnancy. Immunohistochemistry showed that EP2 and COX-2 proteins were colocalized in most cell types of placentome CAR, endometrium, and myometrium. Our study indicates that EP2 is the primary cAMP-generating PGE2 receptor expressed in uteroplacental tissues during bovine pregnancy. Temporal and tissue-specific expression of PGE2 and PGF2
receptors and COX-1 and -2 at the maternal-fetal interface suggests a selective and distinctive role for PGE2 and PGF2
in uterine activities during pregnancy in bovine.
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