Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2004-10-18
pubmed:abstractText
Recognition and establishment of pregnancy involve several molecular and cellular interactions among the conceptus, uterus, and corpus luteum (CL). In ruminants, interferon-tau (IFNtau) of embryonic origin is recognized as the pregnancy recognition signal. Endometrial prostaglandin F(2alpha) (PGF(2alpha)) is the luteolysin, whereas PGE(2) is considered a luteoprotective or luteotrophic mediator at the time of establishment of pregnancy. The interplay between IFNtau and endometrial PGs production, transport, and signaling at the time of maternal recognition of pregnancy (MRP) is not well understood. We have studied the expression of enzymes involved in metabolism of PGE(2) and PGF(2alpha), cyclooxygenase-1 (COX-1) and COX-2, PG synthases (PGES and PGFS), PG 15-dehydrogenase, and PG transporter as well as PGE(2) (EP2 and EP3) and PGF(2alpha) receptors. IFNtau influences cell-specific expression of COX-2, PGFS, EP2, and EP3 in endometrium, myometrium, and CL in a spatio-temporal and tissue-specific manner, whereas it does not alter COX-1, PGES, PG 15-dehydrogenase, PG transporter, or PGF(2alpha) receptor expression in any of these tissues. In endometrium, IFNtau decreases PGFS in epithelial cells and increases EP2 in stroma. In myometrium, IFNtau decreases PGFS and increases EP2 in smooth muscle cells. In CL, IFNtau increases PGES and decreases EP3. Together, our results show that IFNtau directly or indirectly increases PGE(2) biosynthesis and EP2-associated signaling in endometrium, myometrium, and CL during MRP. Thus, PGE(2) may play pivotal roles in endometrial receptivity, myometrial quiescence, and luteal maintenance, indicating polycrine (endocrine, exocrine, paracrine, and autocrine) actions of PGE(2) at the time of MRP. Therefore, the establishment of pregnancy may depend not only on inhibition of endometrial PGF(2alpha), but also on increased PGE(2) production in cattle.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/15-hydroxyprostaglandin..., http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 1, http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2, http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone, http://linkedlifedata.com/resource/pubmed/chemical/Hydroxyprostaglandin Dehydrogenases, http://linkedlifedata.com/resource/pubmed/chemical/Interferon Type I, http://linkedlifedata.com/resource/pubmed/chemical/Intramolecular Oxidoreductases, http://linkedlifedata.com/resource/pubmed/chemical/Isoenzymes, http://linkedlifedata.com/resource/pubmed/chemical/Pregnancy Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandin-Endoperoxide Synthases, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Prostaglandin, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Prostaglandin E, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Prostaglandin E, EP2..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Prostaglandin E, EP3..., http://linkedlifedata.com/resource/pubmed/chemical/prostaglandin F2alpha receptor, http://linkedlifedata.com/resource/pubmed/chemical/prostaglandin-E synthase, http://linkedlifedata.com/resource/pubmed/chemical/prostaglandin-F synthase, http://linkedlifedata.com/resource/pubmed/chemical/trophoblastin
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0013-7227
pubmed:author
pubmed:issnType
Print
pubmed:volume
145
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5280-93
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:15308607-Animals, pubmed-meshheading:15308607-Cattle, pubmed-meshheading:15308607-Cyclooxygenase 1, pubmed-meshheading:15308607-Cyclooxygenase 2, pubmed-meshheading:15308607-Dinoprostone, pubmed-meshheading:15308607-Endometrium, pubmed-meshheading:15308607-Female, pubmed-meshheading:15308607-Gene Expression, pubmed-meshheading:15308607-Hydroxyprostaglandin Dehydrogenases, pubmed-meshheading:15308607-Interferon Type I, pubmed-meshheading:15308607-Intramolecular Oxidoreductases, pubmed-meshheading:15308607-Isoenzymes, pubmed-meshheading:15308607-Myometrium, pubmed-meshheading:15308607-Pregnancy, pubmed-meshheading:15308607-Pregnancy, Animal, pubmed-meshheading:15308607-Pregnancy Proteins, pubmed-meshheading:15308607-Prostaglandin-Endoperoxide Synthases, pubmed-meshheading:15308607-RNA, Messenger, pubmed-meshheading:15308607-Receptors, Prostaglandin, pubmed-meshheading:15308607-Receptors, Prostaglandin E, pubmed-meshheading:15308607-Receptors, Prostaglandin E, EP2 Subtype, pubmed-meshheading:15308607-Receptors, Prostaglandin E, EP3 Subtype, pubmed-meshheading:15308607-Signal Transduction
pubmed:year
2004
pubmed:articleTitle
Effect of interferon-tau on prostaglandin biosynthesis, transport, and signaling at the time of maternal recognition of pregnancy in cattle: evidence of polycrine actions of prostaglandin E2.
pubmed:affiliation
Unité d'Ontogénie et Reproduction, Centre de Recherche du Centre Hospitalier Universitaire de Québec, Centre Hospitalier de l'Université de Laval, 2705 boulevard Laurier, Ste-Foy, Québec, Canada.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't