Fetal-to-maternal progression of prostaglandin H-2 synthase-2 expression in ovine intrauterine tissues during the course of labor

Citation
S. Gyomorey et al., Fetal-to-maternal progression of prostaglandin H-2 synthase-2 expression in ovine intrauterine tissues during the course of labor, BIOL REPROD, 62(3), 2000, pp. 797-805
Citations number
49
Categorie Soggetti
da verificare
Journal title
BIOLOGY OF REPRODUCTION
ISSN journal
00063363 → ACNP
Volume
62
Issue
3
Year of publication
2000
Pages
797 - 805
Database
ISI
SICI code
0006-3363(200003)62:3<797:FPOPHS>2.0.ZU;2-J
Abstract
We examined whether spontaneous parturition in sheep was associated with ti ssue-specific changes in prostaglandin H-2 synthase-2 (PGHS-2) expression a nd/or with altered expression of myometrial EP and FP receptors, Placental and uterine tissues were collected from three groups of chronically cathete rized sheep in relation to term spontaneous labor: late pregnancy, not in l abor; early labor; and active labor. Expression of PGHS-2 mRNA and protein was determined by in situ hybridization, Western blotting, and immunohistoc hemistry. Semiquantitative reverse transcription-polymerase chain reaction was used to assess the presence of and changes in prostaglandin (PG) recept or subtypes. In placenta, PGHS-2 mRNA and protein localized to trophoblast uninucleate cells and tended to increase with early labor. PGHS-2 mRNA and protein localized to endometrial epithelium and to myometrium, where PGHS-2 protein levels rose in active labor tissues, Concentrations of PGE(2) in f etal plasma rose progressively with labor, whereas 13,14-dihydro-15-keto-PG F(2 alpha) in maternal plasma increased significantly only in active labor. Messenger RNA encoding four EP receptor subtypes and FP receptor were pres ent: in myometrium, but levels did not change with labor, We suggest that s pontaneous labor in sheep is associated with a progressive increase in PGHS -2 expression in a temporal and tissue-specific manner from trophoblast to maternal tissues, rather than alteration in PG receptor gene expression.