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and ß in Rat Pituitary Gland Detected by Immunohistochemistry
Department of Nature Medicine, Atomic Bomb Disease Institute (E.N., S.Y.), and the Departments of Pharmacology I (Y.N.) and Histology and Cell Biology (T.K.), Nagasaki University School of Medicine, Nagasaki 852-8523; and the Department of Biochemistry, Saitama Medical School (S.I., H.H., M.M.), Saitama 350-0495, Japan
Address all correspondence and requests for reprints to: Eijun Nishihara, M.D., Department of Nature Medicine, Atomic Bomb Disease Institute, Nagasaki University School of Medicine, Sakamoto 112-4, Nagasaki 852-8523, Japan. E-mail: eijun-ngs{at}umin.ac.jp
The physiological effects of estrogen on the pituitary, including
cellular proliferation and regulation of hormone synthesis, are
mediated by the nuclear estrogen receptor (ER). The purpose of this
study was to determine ontogenetic expression of two types of ERs
(ER
and ERß) in the pituitary using specific antibodies,
monoclonal antibody (1D5) for ER
and polyclonal antibody generated
against ERß. First, we confirmed the detection of 66- and 55-kDa
bands for ER
and ERß, respectively, in the rat pituitary extract
by Western blotting. Then immunostaining with these antibodies was
performed using fetal and adult Wistar rat tissues, combined with PRL
or LHß immunohistochemistry. Intense ERß signal was detected
throughout the pituitary from day 12 of gestation. However, staining
for ER
only became detectable from day 17 of gestation. In contrast
with the fetal period, nuclei stained for ER
were widely distributed
in the anterior lobe in the adult rat, whereas ERß-positive cells
were restricted in the anterior lobe. LHß, but not PRL, was
colocalized in ERß-positive cells. Our results indicated that the
major population of ER subtypes in the rat pituitary gland has changed
around the day of birth and that the expression of ERß may be
involved in the differentiation of pituitary cell function to
synthesize a specific hormone.
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