J. Murdoch et al., Hormonal control of urokinase plasminogen activator secretion by sheep ovarian surface epithelial cells, BIOL REPROD, 61(6), 1999, pp. 1487-1491
Secretion of urokinase plasminogen activator (uPA) by ovarian surface epith
elium (OSE) adjacent to the preovulatory ovine follicle has been implicated
in apical tissue degradation and follicular rupture. In vitro experiments
were designed to test the hypothesis that uPA release by OSE is under direc
t hormonal control. Epithelial cells were isolated from the ovarian surface
of sheep using a polytetrafluorethylene scraper designed to dislodge adher
ent cells from culture flasks. Amidolytic cleavage of a uPA-specific chromo
gen (carbobenzoxy-L-gamma-glutamyl [alpha-ot-but]-glycyl-arginine-p-nitroan
ilide monoacetate) was used as a measure of enzymatic bioactivity in OSE-co
nditioned incubation media. Secretion of uPA by OSE suspensions from proest
rous ewes was stimulated by exposure (2 h) to a preovulatory surge-like con
centration of LH. OSE cells obtained during the luteal phase or anestrus we
re not responsive to LH. Baseline rates of uPA secretion and expression of
estradiol receptors (in situ immunofluorescence detection) were not affecte
d by reproductive status. Induction of uPA secretion by anestrous OSE was a
ttained after priming (6 h) with estradiol-17 beta; responsiveness was attr
ibuted to gonadotropin receptor (ligand binding) up-regulation. Monolayers
of OSE established on polyethylene membranes secreted uPA predominately in
a basal (i.e., toward the substratum) direction. We suggest that OSE in jux
taposition with the (hyperemic) wall of the preovulatory follicle is perfus
ed by surge levels of LH, invoking uPA release into underlying ovarian tiss
ues.