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
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
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.