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Division of Reproductive Sciences, Oregon Regional Primate Research Center (C.L.C., R.L.S., D.M.D.), Beaverton, Oregon 97006; and the Department of Physiology and Pharmacology, Oregon Health Sciences University (R.L.S.), Portland, Oregon 97201
Address all correspondence and requests for reprints to: Dr. R. L. Stouffer, Division of Reproductive Sciences, Oregon Regional Primate Research Center, 505 NW 185th Avenue, Beaverton, Oregon 97006. E-mail: stouffri{at}ohsu.edu
Although steroids play a local role(s) in ovulation and luteinization
of the primate follicle, the dynamics of steroid receptor expression
during the 36- to 38-h periovulatory interval has yet to be elucidated.
The present study examines the regulation of messenger RNAs (mRNAs) for
progesterone (PR), androgen (AR), and estrogen (ER
, ERß) receptors
as well as the aryl hydrocarbon receptor (AhR) in macaque granulosa
cells during controlled ovarian stimulation cycles before (0 h)
and after (up to 36 h) administration of the ovulatory hCG bolus
with or without steroid depletion and progestin replacement. All
steroid receptor mRNAs were detected in granulosa cells before the
ovulatory stimulus, as determined by RT-PCR. PR mRNA increased
(P < 0.05) by 12 h after hCG; 24 and 36
h after hCG, levels were intermediate between 012 h. PR mRNA was
reduced by steroid depletion throughout the periovulatory interval
(P < 0.05); however, progestin replacement
returned PR mRNA to control levels at 12 h. AR mRNA increased
(P < 0.05) at 24 h post-hCG and remained at
this level 36 h after hCG; steroid depletion did not alter AR mRNA
levels. ER
mRNA did not change, whereas ERß decreased 1236 h
after the ovulatory stimulus (P < 0.05). Steroid
depletion reduced ER
mRNA 12 h after hCG, an effect partially
reversible by progestin replacement, whereas ERß mRNA was not
affected by steroids. AhR mRNA was undetectable before the
administration of hCG, but increased by 12 h
(P < 0.05). These data demonstrate hCG-initiated,
steroid-dependent (PR, ER
) and -independent (AR, ERß, AhR)
expression of receptor mRNAs in primate granulosa cells during the
periovulatory interval. Differences in patterns of expression may
relate to diverse roles for steroid hormones and AhR ligands in
periovulatory events.
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