Literature DB >> 4374940

High-affinity binding of oestradiol-17beta by cytosols from testis interstitial tissue, pituitary, adrenal, liver and accessory sex glands of the male rat.

W M van Beurden-Lamers, A O Brinkmann, E Mulder, H J van der Molen.   

Abstract

The specificity of the binding of oestradiol-17beta by cytoplasmic fractions of several tissues of the male rat was investigated. 1. Agar-gel electrophoresis, Sephadex chromatography, adsorption by dextran-coated charcoal and sucrose-gradient centrifugation were used to estimate the binding capacity and specificity. The four different methods all gave similar results for the capacity of the specific oestradiol-17beta-binding macromolecules in the testis. 2. The presence of a specific saturable binding protein with a sedimentation coefficient of 8S was demonstrated in liver, adrenal, pituitary, prostate, epididymis and testis interstitial tissue. The highest concentration of oestradiol-17beta-binding macromolecules was found in testis interstitial tissue (0.12pmol/mg of protein) and in the pituitary (0.075pmol/mg of protein). 3. The oestradiol-17beta receptor in the testis cytosol showed the characteristics of a protein with respect to Pronase treatment and temperature sensitivity. In competition experiments with different steroids the receptor showed a high affinity for oestradiol-17beta, a moderate affinity for diethylstilboestrol and oestradiol-17alpha and a low affinity for oestrone, oestriol, testosterone and 5alpha-dihydrotestosterone (17beta-hydroxy-5alpha-androstan-3-one). 4. The wide distribution of oestradiol-17beta receptors in the male rat is in apparent contradiction to the current concept of the specificity of steroid-hormone action. Further research is required to investigate a possible physiological meaning of the presence of specific receptors in the different tissues.

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Year:  1974        PMID: 4374940      PMCID: PMC1168027          DOI: 10.1042/bj1400495

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  25 in total

1.  Cellular localization of 3H-oestradiol in the hypothalamus. An autoradiographic study in male and female rats.

Authors:  A Attramadal
Journal:  Z Zellforsch Mikrosk Anat       Date:  1970

2.  Metabolism of sex hormones in the aortic wall.

Authors:  A Chobanian; P I Brecher; R D Lille; H H Wotiz
Journal:  J Lipid Res       Date:  1968-11       Impact factor: 5.922

3.  Decreased estradiol binding in the uterus and anterior hypothalamus of androgenized female rats.

Authors:  P Tuohimaa; R Johansson
Journal:  Endocrinology       Date:  1971-05       Impact factor: 4.736

4.  Comparative binding affinity of estrogens and its relation to estrogenic potency.

Authors:  S G Korenman
Journal:  Steroids       Date:  1969-02       Impact factor: 2.668

5.  Nuclear concentration of 3H-estradiol in target tissues. Dry-mount autoradiography of vagina, oviduct, ovary, testis, mammary tumor, liver and adrenal.

Authors:  W E Stumpf
Journal:  Endocrinology       Date:  1969-07       Impact factor: 4.736

6.  A receptor molecule for estrogens: studies using a cell-free system.

Authors:  D Toft; G Shyamala; J Gorski
Journal:  Proc Natl Acad Sci U S A       Date:  1967-06       Impact factor: 11.205

7.  A receptor molecule for estrogens: isolation from the rat uterus and preliminary characterization.

Authors:  D Toft; J Gorski
Journal:  Proc Natl Acad Sci U S A       Date:  1966-06       Impact factor: 11.205

8.  Hypothalamic and hypophyseal estradiol-binding complexes.

Authors:  T F Mowles; B Ashkanazy; E Mix; H Sheppard
Journal:  Endocrinology       Date:  1971-08       Impact factor: 4.736

9.  Interaction of uterus cytosol receptor with estradiol. Equilibrium and kinetic studies.

Authors:  H Truong; E E Baulieu
Journal:  Biochim Biophys Acta       Date:  1971-04-20

10.  Uptake of (6,7-3H) estradiol-17 beta by the hypothalamus, pituitary and other organs of rats in different conditions of hormonal status.

Authors:  K N Rao; G P Talwar
Journal:  Indian J Biochem       Date:  1969-06
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  11 in total

1.  Cloning of a novel receptor expressed in rat prostate and ovary.

Authors:  G G Kuiper; E Enmark; M Pelto-Huikko; S Nilsson; J A Gustafsson
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-11       Impact factor: 11.205

2.  Gastric estrogen increases pituitary estrogen receptor α and prolactin mRNAs during the different pathological conditions of the liver.

Authors:  Hiroto Kobayashi; Saori Yoshida; Ying-Jie Sun; Nobuyuki Shirasawa; Akira Naito
Journal:  Endocrine       Date:  2012-07-28       Impact factor: 3.633

3.  Bromocriptine and sulpiride competitively inhibit estrogen binding to its receptor in the adrenal gland.

Authors:  I A Lüthy; R S Calandra
Journal:  Experientia       Date:  1986-02-15

4.  Binding of dihydrotestosterone to a nuclear-envelope fraction from the male rat liver.

Authors:  Y A Lefebvre; S J Morante
Journal:  Biochem J       Date:  1982-01-15       Impact factor: 3.857

5.  Ontogeny of the sex steroid and prolactin receptors in the male rat adrenal gland.

Authors:  I A Lüthy; R S Calandra
Journal:  Experientia       Date:  1984-09-15

6.  Fluorescent ligands, used in histocytochemistry, do not discriminate between estrogen receptor-positive and receptor-negative human tumor cell lines.

Authors:  E M Berns; E Mulder; F F Rommerts; R A Blankenstein; E de Graaf; H J van der Molen
Journal:  Breast Cancer Res Treat       Date:  1984       Impact factor: 4.872

7.  The developmental profile of lactoferrin in mouse epididymis.

Authors:  L C Yu; Y H Chen
Journal:  Biochem J       Date:  1993-11-15       Impact factor: 3.857

8.  Comparative study of nuclear binding sites for oestradiol in rat testicular and uterine tissue. Determination of low amounts of specific binding site by an [3H] oestradiol-exchange method.

Authors:  W de Boer; J de Vries; E Mulder; H J van der Molen
Journal:  Biochem J       Date:  1977-02-15       Impact factor: 3.857

9.  Functional development of sex accessory organs of the male rat. Use of oestradiol benzoate to identify the neonatal period as critical for development of normal protein-synthetic and secretory capabilities.

Authors:  S J Higgins; D E Brooks; F M Fuller; P J Jackson; S E Smith
Journal:  Biochem J       Date:  1981-03-15       Impact factor: 3.857

10.  Estradiol and Estrogen Receptor Agonists Oppose Oncogenic Actions of Leptin in HepG2 Cells.

Authors:  Minqian Shen; Haifei Shi
Journal:  PLoS One       Date:  2016-03-16       Impact factor: 3.240

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