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Departments of Biochemistry and Animal Sciences, University of Wisconsin Madison, Wisconsin 53706
Address requests for reprints to: Dr. Jack Gorski, Department of Biochemistry, University of Wisconsin-Madison, 420 Henry Mall, Madison, Wisconsin 53706.
Abstract
When cultured rat uterine cells were treated for up to 6 h with 5 nM 17β-estradiol, no decrease in the [3H] estradiol-binding capacity of the cells was observed (i.e. no processing). This was true whether the cells were treated directly with 5 nM [3H]estradiol or with 5 nM unlabeled 17β-estradiol followed by homogenization and exchange with [3H]estradiol in vitro. In additional experiments, intact cells were treated with medium containing 5 nM [3H]estradiol for 30 min, and then that medium was removed and replaced with medium containing 5 nM unlabeled 17β-estradiol. Receptor-bound estradiol in intact cells was totally exchangeable with estradiol in the culture medium (t
90 min). Six-hour treatment of cells with 5 nM 17β-estradiol led to a 50% increase in the [3H]progesterone-binding capacity of the cells, while no loss of estrogen-binding capacity occurred. These results indicate that progesterone receptors can be induced by estrogen in the rat uterus in the absence of estrogen receptor processing. (Endocrinology 118: 603–608, 1986)
Footnotes
* This work was supported in part by the College of Agricultural and Life Sciences, University of Wisconsin, Madison; NIH Grant HD-08192, and NIH Training Grant 5T32-GM07215 (to J.K.). This is paper 830 from the Department of Meat and Animal Science.
Received October 24, 1984.
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