Summary:
Although numerous clinical studies have demonstrated the beneficial effect of preventing
postmenopausal bone loss in elder women by long-term estrogen administration, effects
of estrogen at the cellular level still remain unclear. Efforts to determine the precise
role of bone cells in estrogen-mediated pathways are often hampered by the lack of
suitable cell culture models. Presuming that sex steroids have a direct, stimulating
effect on bone cells in vitro, we investigated the influence of 17β -estradiol, testosterone and 1,25(OH)2 D3 on cell proliferation and differentiation using four established human osteosarcoma
(HOS) cell lines of different gender of the donors (male origin: MG 63, HOS 58; female
origin: SaOS 2, TE 85). These cell lines are believed to represent different stages
of osteogenic maturation. Thus, the aim of this study was to clarify if possible responses
to sex steroids are related to gender or osteogenic commitment of the individual cell
culture. HOS cells were cultured in six-well plates and underwent hormone treatment
(1 nM and 10 nM 17β -estradiol, 0.1 nM and 1 nM testosterone and 1 μM 1,25(OH)2 D3 ) for 48 h hours. Cell proliferation was determined by measuring total cell numbers.
Cell function was studied by measuring alkaline phosphatase activity and secreted
osteocalcin. In this study, estrogen significantly increased proliferation of both
one male (MG 63) and one female (SaOS 2) cell line, but decreased proliferation of
the female HOS TE 85 cell line significantly. Testosterone treatment had a positive
effect on proliferation of only one female cell line (SaOS 2). A significant increase
of alkaline phosphatase activity in SaOS 2 and HOS 58 cells and of osteocalcin levels
in SaOS 2 cells was detected following estrogen treatment. Administration of 1,25(OH)2 D3 was followed by an increased cell proliferation in HOS 58, MG 63 and SaOS 2. Significant
gender-related differences could not be demonstrated. In conclusion, response to hormonal
treatment with sex steroids is not related to the gender of the osteosarcoma cell
line, but rather depends on its osteoblastic commitment.
Key words:
Bone cells - osteosarcoma - differentiation - estrogen - testosterone - menopause
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Prof. Dr. med. Andreas Schulz
Institute of Pathology
Justus-Liebig-University Giessen
Langhansstrasse 10
D-35385 Giessen
Germany
Phone: +49-6 41-9 94 11 00
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Email: andreas.schulz@patho.med.uni-giessen.de