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BOR - Papers in Press, published online ahead of print November 27, 2002.
Biol Reprod 2002, 10.1095/biolreprod.102.009266
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BIOLOGY OF REPRODUCTION 68, 1054–1063 (2003)
DOI: 10.1095/biolreprod.102.009266
© 2003 by the Society for the Study of Reproduction, Inc.


Testis

Stimulatory Effect of Progesterone on the Expression of Steroidogenic Acute Regulatory Protein in MA-10 Leydig Cells1

Heidi Schwarzenbacha, Pulak R. Mannab, Douglas M. Stoccob, Gopa Chakrabartia, and Amal K. Mukhopadhyay2,a

a Institute for Hormone and Fertility Research, University of Hamburg, D-22529 Hamburg, Germany b Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas 79430

The steroidogenic acute regulatory protein (StAR), by virtue of its ability to facilitate the intramitochondrial transport of cholesterol, plays an important role in regulating steroid hormone biosynthesis in steroidogenic cells. In agreement with published data, both StAR expression and progesterone production in MA-10 mouse Leydig tumor cells could be stimulated with hCG and 8Br-cAMP. Addition of aminoglutethimide, an inhibitor of cholesterol side chain cleavage (P450scc) enzyme, not only resulted in a drastic inhibition of progesterone production but also in an attenuation of StAR expression in response to either hCG or 8-Br-cAMP. Therefore, we addressed the question of whether progesterone, the end product of the steroidogenic cascade in these cells, could be in a position to regulate the StAR gene expression. In MA-10 cells, we report here that progesterone in microgram amounts can induce StAR gene expression in a time- and dose-dependent manner. StAR expression in response to a maximally effective concentration of progesterone of 10 µg/ml was highest at 6 h and started decreasing thereafter. The effect of progesterone on StAR protein and StAR mRNA induction was mimicked by its synthetic analog, progestin R5020, but not by other steroids, including dexamethasone, estradiol, testosterone, and dihydrotestosterone. Dexamethasone, in contrast, was able to inhibit StAR expression in MA-10 cells. Surprisingly, RU486, a potent antagonist of progesterone and glucocorticoid action, had a stimulatory effect on StAR mRNA levels. Reverse transcription-polymerase chain reaction analysis demonstrated the absence of the classical form of progesterone receptor in MA-10 cells. Thus, for the first time, a direct stimulatory effect of a steroid on StAR gene expression has been demonstrated. Furthermore, these results provide a new insight, indicating that progesterone mediates the activation of StAR expression exerted presumably through a novel, nonclassical progesterone receptor in mouse Leydig cells.

1 We gratefully acknowledge the financial support of the Leidenberger-Müller-Foundation, Hamburg, Germany, to A.K.M. Also, financial support was obtained from NIH grant HD 17481 and from the Robert A. Welch Foundation (to D.M.S.).

2 Correspondence: Amal K. Mukhopadhyay, Institute for Hormone and Fertility Research, Grandweg 64, D-22529 Hamburg, Germany. FAX: 49 40 56 19 08 64; e-mail: amal{at}ihf.de




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