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Takeshi Kurita, Ki-jun Lee, Paul S. Cooke, John P. Lydon, Gerald R. Cunha, Paracrine Regulation of Epithelial Progesterone Receptor and Lactoferrin by Progesterone in the Mouse Uterus, Biology of Reproduction, Volume 62, Issue 4, 1 April 2000, Pages 831–838, https://doi.org/10.1095/biolreprod62.4.831
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Abstract
The objective of this study was to determine whether uterine stromal and/or epithelial progesterone receptor (PR) is required for the antagonism by progesterone (P4) of estradiol-17β (E2) action on expression of PR and lactoferrin in uterine epithelium. Uterine tissue recombinants were prepared with epithelium (E) and stroma (S) from wild-type (wt) and PR knockout (PRKO) mice: wt-S+wt-E and PRKO-S+wt-E. P4 action on epithelial PR expression was studied in wt-S+wt-E and PRKO-S+wt-E tissue recombinants. E2 down-regulated epithelial PR in both types of tissue recombinants, but P4 blocked E2-induced down-regulation of epithelial PR only in wt-S+wt-E tissue recombinants. Thus, P4 requires stromal PR to inhibit E2-induced down-regulation of epithelial PR. Epithelial PR is not sufficient in itself. The inhibitory effect of P4 on lactoferrin expression was studied in 4 types of tissue recombinants (wt-S+wt-E, PRKO-S+wt-E, wt-S+PRKO-E, and PRKO-S+PRKO-E). E2 induced lactoferrin in all 4 types of tissue recombinants. P4 blocked E2-induced lactoferrin expression only in wt-S+wt-E tissue recombinants. In wt-S+PRKO-E tissue recombinants, P4 inhibited lactoferrin expression only partially. P4 failed to block E2-induced lactoferrin expression in PRKO-S+wt-E and PRKO-S+PRKO-E tissue recombinants. Thus, both epithelial and stromal PR are essential for full P4 inhibition of E2-induced lactoferrin expression.