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J. Biol. Chem., Vol. 259, Issue 5, 2697-2700, 03, 1984
CR Lyttle, KL Medlock and DM Sheehan
Rat uterine nuclei have been reported to contain two types of estrogen
binding sites (I and II). Type I is the classical high affinity, low
capacity translocatable estrogen receptor, while type II is a lower
affinity non-translocatable binding site. Correlation of data on hormonal
specificity of induction and inhibition, tissue and cellular localization,
and ontogenic appearance for type II binding sites and eosinophils
suggested the hypothesis that these binding sites are associated with
eosinophils. Although type II sites are reported to be highly correlated
with uterine growth, premature growth can be elicited in newborn rats by
five daily estradiol injections without the appearance of type II sites.
Under these conditions, no eosinophils, as measured by peroxidase activity,
are found. However, multiple estradiol injections on postnatal days 6-10 or
10-14 increased the levels of both type II sites and eosinophils.
Eosinophils, purified from a peritoneal lavage, were found to contain a low
affinity binding site with characteristics similar to type II binding
sites. Short term estrogen- treated rat uteri contain only type I nuclear
receptor and low levels of eosinophils while long term estrogen-treated rat
uteri contain both type I and type II nuclear binding sites as well as
approximately 6 X 10(5) eosinophils/uterus. The addition of this number of
purified eosinophils to short term treated uteri resulted in saturation
curves and Scatchard plots identical to those seen in long term treated
uteri. These data indicate that the type II nuclear binding site is
transported into the uterus with eosinophils following estrogen treatment.
Eosinophils as the source of uterine nuclear type II estrogen binding sites
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