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PMID: 3388021 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Evidence of estrogen receptors in normal human osteoblast-like cells.

Science (New York, N.Y.) ·Vol. 241 ·No. 4861 ·1988-07-01 ·Pages 84-6

Eriksen EF, Colvard DS, Berg NJ, Graham ML, Mann KG, Spelsberg TC, Riggs BL

Abstract

In seven strains of cultured normal human osteoblast-like cells, a mean of 1615 molecules of tritium-labeled 17 beta-estradiol per cell nucleus could be bound to specific nuclear sites. The nuclear binding of the labeled steroid was temperature-dependent, steroid-specific, saturable, and cell type-specific. These are characteristics of biologically active estrogen receptors. Pretreatment with 10 nanomolar estradiol in vitro increased the specific nuclear binding of progesterone in four of six cell strains, indicating an induction of functional progesterone receptors. RNA blot analysis demonstrated the presence of messenger RNA for the human estrogen receptor. The data suggest that estrogen acts directly on human bone cells through a classical estrogen receptor-mediated mechanism.

MeSH Terms
Binding, Competitive Cell Nucleus/metabolism Cells, Cultured DNA/genetics Dexamethasone/metabolism Diethylstilbestrol/metabolism Estradiol/metabolism,pharmacology Humans Nucleic Acid Hybridization Osteoblasts/drug effects,metabolism Progesterone/metabolism Promegestone/metabolism RNA, Messenger/metabolism Receptors, Estrogen/drug effects,genetics,metabolism Receptors, Progesterone/drug effects,metabolism Tritium
Chemicals
RNA, Messenger Receptors, Estrogen Receptors, Progesterone Tritium Progesterone Estradiol Diethylstilbestrol Dexamethasone DNA Promegestone
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Eriksen E F
Endocrine Research Unit, Mayo Clinic, Rochester, MN 55905.
Colvard D S
Berg N J
Graham M L
Mann K G
Spelsberg T C
Riggs B L
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-07-01
Pages
84-6
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIA NIH HHS · AG-04875 · United States
NCI NIH HHS · CA-90441 · United States
NICHD NIH HHS · HD-9140 · United States
Analysis Services
Analysis Services

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