Genomic and non-genomic effects of progesterone and pregnenolone on the function of bovine endometrial cells
M.K. Kowalik, D. Slonina, J. Kotwicahttps://doi.org/10.17221/58/2009-VETMEDCitation:Kowalik M.K., Slonina D., Kotwica J. (2009): Genomic and non-genomic effects of progesterone and pregnenolone on the function of bovine endometrial cells. Veterinarni Medicina, 54: 205-214.
Progesterone (PKeywords:non-genomic effect; progesterone; progesterone membrane receptor component 1; endometrium; bovine
) decreases oxytocin (OT)-stimulated prostaglandin (PG)F2α, but not PGE2 secretion from bovine endometrial cells and this effect is partly elicited via a non-genomic route. The aim of this study was to determine whether P4 and pregnenolone (P5), in the presence or absence of OT, influence: (a) the gene expression of enzymes responsible for PGs synthesis: cyclooxygenase-2 (COX-2), synthase of PGF2α (PGFS) and PGE=sub>2 (PGES), (b) protein expression of COX-2, PGFS and PGES, and (c) P4 receptor membrane component 1 (PGRMC1) gene expression in bovine endometrial cells. The epithelial endometrial cells (2.5 × 105/ml) from Days 14–16 of the oestrous cycle were incubated for 72–96 h to attach the cells to the bottom of a well. Next, the cells were preincubated for 30 min with P4 and P5 (10–5M each) and incubated for 4 h and 6 h alone or with OT (10–7M). Thereafter, the medium was collected for PGE2 and PGFM determination, while cells were harvested for gene and protein expression analysis. The used steroids: (a) inhibited OT-stimulated PGF2α, but not PGE2 secretion from endometrial cells, (b) did not affect the expression of mRNA for COX-2, PGFS, PGES and PGRMC1 in endometrial cells after 4 and 6 h, (c) they decreased OT-stimulated COX-2 mRNA expression only after 6 h incubation, and (d) did not influence COX-2, PGFS and PGES protein expression after 6 h. These results indicate that P4 and P5 inhibit OT-stimulated secretion/production of luteolytic PGF2α by a transcription-independent mechanism and partly by down-regulation of COX-2 mRNA.