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J Biol Chem, Vol. 274, Issue 53, 37982-37989, December 31, 1999

Rat Decidual Prolactin
IDENTIFICATION, MOLECULAR CLONING, AND CHARACTERIZATION*

Anne Prigent-Tessier, Christian Tessier, Mitsuko Hirosawa-Takamori, Catherine Boyer, Susan Ferguson-Gottschall, and Geula GiboriDagger

From the Department of Physiology and Biophysics, College of Medicine, University of Illinois, Chicago, Illinois 60612

Establishment and maintenance of pregnancy require the activity of a highly specialized maternal tissue, the decidua. It is well established that the human decidua synthesizes and releases prolactin. However, in the rat, no study has been able to demonstrate the production of prolactin by the decidua. In this report, we established for the first time using Northern blot analysis and reverse transcription-polymerase chain reaction, Western blot analysis, immunocytochemistry, and enzyme-linked immunosorbent assay, that a defined cell population located in the rat antimesometrial decidua expresses prolactin mRNA, as well as synthesizes and secretes this hormone. By reverse transcription-polymerase chain reaction and rapid amplification of cDNA ends, we cloned a full-length cDNA for rat decidua prolactin, whose sequence was identical to that of pituitary prolactin. Our results also showed that pituitary prolactin appeared to down-regulate decidual prolactin levels. Under these circumstances, inhibition of pituitary prolactin secretion led to a rise in both decidual prolactin mRNA and protein expression. Moreover, addition of exogenous prolactin to primary decidual cells in culture also caused a marked decrease in decidual prolactin mRNA expression. Finally, treatment of primary decidual cells with steroid hormones or 8-bromo-cAMP revealed a differential regulation of decidual prolactin expression from that of pituitary suggesting a tissue-specific regulation of prolactin gene expression, possibly through the use of an alternative promoter in rat decidua.


* This work was supported by National Institutes of Health Grant HD-12356 (to G. G.) and a grant from the Ernst Schering Research Foundation (to C. T.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence and reprints requests should be addressed: Dept. of Physiology and Biophysics (M/C 901), University of Illinois, 835 S. Wolcott Ave., Chicago, IL 60612-7342. Tel.: 312-996-7688; Fax: 312-996-1414; E-mail: ggibori@uic.edu.


Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.
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