PLASMINOGEN-ACTIVATOR PRODUCTION BY THE GRANULOSA LAYER IS STIMULATEDBY FACTOR(S) PRODUCED BY THE THECA LAYER AND INHIBITED BY THE LUTEINIZING-HORMONE SURGE IN THE CHICKEN

Citation
Ja. Jackson et al., PLASMINOGEN-ACTIVATOR PRODUCTION BY THE GRANULOSA LAYER IS STIMULATEDBY FACTOR(S) PRODUCED BY THE THECA LAYER AND INHIBITED BY THE LUTEINIZING-HORMONE SURGE IN THE CHICKEN, Biology of reproduction, 50(4), 1994, pp. 812-819
Citations number
28
Categorie Soggetti
Reproductive Biology
Journal title
ISSN journal
00063363
Volume
50
Issue
4
Year of publication
1994
Pages
812 - 819
Database
ISI
SICI code
0006-3363(1994)50:4<812:PPBTGL>2.0.ZU;2-Q
Abstract
The stages of follicular maturation of a preovulatory follicle in the hen can bc divided into an extended proliferative phase (prior to LH s urge) and a brief ovulatory phase (after LH surge). Previous studies s uggest involvement of plasminogen activator (PA) in both the prolifera tive and ovulatory phases. The goals of the present study were 1) to d etermine whether PA production by granulosa and theca is dependent upo n interaction of the two cell layers; 2) to investigate whether the st ructural difference of the stigma (site of follicular rupture) and non stigma regions of the theca layer affect PA production; 3) to determin e whether there is a change in the ability of the granulosa layer and stigma or nonstigma regions of the theca layer to produce PA as the fo llicle makes the transition from the proliferative to the ovulatory ph ase; and 4) to characterize the type(s) of PA produced by the hen foll icle. Equal proportions of the granulosa layer (10-mm diameter) and st igma or nonstigma regions of the theca layer (10 mg) obtained from the F1 preovulatory follicle 8 h before ovulation (before LH surge) or 2 h before ovulation (after LH surge) were incubated alone or in combina tion for 24 h. PA was measured in tissue homogenates and medium by use of the chromogenic substrate S-225 1. The granulosa layer or stigma o r nonstigma regions of the theca layer incubated alone and obtained ei ther 8 h or 2 h before ovulation had very low amounts of PA activity i n the medium and tissue homogenates. However, co-incubation of the gra nulosa layer with either stigma or nonstigma regions of the theca laye r dramatically increased the amount of PA activity in the medium when obtained 8 h, but not 2 h, before ovulation. PA activity in the medium was similar whether the granulosa layer was co-incubated with stigma or nonstigma regions of the theca layer. The primary site of PA produc tion was the granulosa layer, which was dependent upon stimulation by factor(s) secreted by the theca layer. To determine the possible role of LH in the regulation of PA activity, the granulosa layer or stigma and nonstigma regions of the theca layer were obtained 8 h before ovul ation (before LH surge) and incubated alone or co-incubated in the pre sence or absence of ovine LH (25 ng/ml). LH substantially decreased th e PA activity in the medium from co-incubation of the granulosa layer with stigma or nonstigma regions of the theca layer. LH had no effect on the ability of the granulosa layer or stigma or nonstigma regions o f the theca layer to produce PA when incubated alone. The type(s) of P A produced by the granulosa layer during the proliferative phase was d etermined by polyacrylamide substrate gel elcctrophoresis and Western blot. Medium from co-incubation of the granulosa layer with stigma or nonstigma regions of the theca layer consistently showed only one band of plasminogen-dependent proteolytic activity with a molecular weight slightly lower than the human urokinase PA (uPA) standard. The Wester n blot showed one band of immunoreactive uPA, which coincided with par tially purified chicken uPA. The present study demonstrates that in th e hen 1) factor(s) from the theca layer stimulate the granulosa layer to produce uPA during the proliferative phase, and 2) the ovulatory LH surge suppresses PA activity resulting from the interaction of granul osa and theca layers. Therefore, the primary role of uPA may be for ti ssue remodeling during follicular growth and maturation.