Regulation of the Rat Oxytocin Gene by Estradiol

• Published in: Journal of neuroendocrinology 1990-10, Vol.2 (5), p.633-639
• Main Authors: Peter, J., Burbach, H., Adan, Roger A. H., van Tol, Hubert H. M., Verbeeck, Marleen A. E., Axelson, John F., van Leeuwen, Fred W., Beekman, Johanna M., Ab, Geert
• Format: Article
• Language: English
• Subjects: estrogen receptor; estrogens; hypothalamo-neurohypophyseal system; oxytocin; vasopressin
• ISSN: 0953-8194; 1365-2826
• DOI: 10.1111/j.1365-2826.1990.tb00458.x

Oxytocin (OT) plays a role in reproduction at the level of the pituitary and mammary glands and uterus. This OT is synthesized in the hypothalamo‐neurohypophyseal system (HNS). A number of observations have suggested that estrogens regulate the production of OT in the HNS. In this study the effect of 17β‐estradiol on the activity of the OT gene promoter was examined as well as the effect of 17β‐estradiol in vivo on OT messenger ribonucleic acid (mRNA) and peptide revels in the rat HNS. Vasopressin (VP) and its mRNA were also determined in the in vivo studies. The direct transcriptional stimulation of OT gene expression by 17β‐estradiol was studied in two different heterologous expression systems. When a plasmid having nucleotides −363 to +16 of the rat OT gene fused to the firefly luciferase reporter gene was co‐transfected with an estrogen receptor expression vector in P19 embryonal carcinoma cells, luciferase activity was stimulated 80‐fold by 17β‐estradiol. In estrogen receptor containing MCF‐7 cells transfected with a plasmid having nucleotides −188 to +16 of the rat OT gene fused to the chloramphenicol acetyl transferase gene, 17β‐estradiol induced the expression of the chloramphenicol acetyl transferase gene through the cloned promoter element. After in vivo treatment of ovariectomized rats with 17β‐estradiol, levels of OT mRNA and VP mRNA were measured in microdissected supraoptic and paraventricular nuclei as well as VP and OT levels in these nuclei and the pituitary gland. As compared to non‐treated ovariectomized rats there was no difference in contents of OT mRNA and VP mRNA in these hypothalamic nuclei and in levels of the peptides in paraventricular nuclei and the pituitary gland. A 30% reduction of the OT content of the supraoptic nuclei only was found, while the VP content did not change. To explain the results immunocytochemical analyses of the hypothalamus were performed, showing that the estrogen receptor was absent in the magnocellular neurons of the supraoptic and paraventricular nuclei. The results demonstrate that the 5’flanking region of the OT gene confers estrogen‐sensitivity to transcription of the OT gene. This potential to respond to estrogens is not used in the OT‐producing neurons of supraoptic and paraventricular nuclei probably due to the absence of the estrogen receptor.