Triiodothyronine, a Regulator of Osteoblastic Differentiation: Depression of Histone H4, Attenuation of c-fos/c-jun, and Induction of Osteocalcin Expression
Autor: | Nadja Fratzl-Zelman, Franz Varga, Klaus Klaushofer, H Glantschnig, Monika Rumpler, E. Luegmayr |
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Rok vydání: | 1997 |
Předmět: |
Endocrinology
Diabetes and Metabolism Osteocalcin Cell Down-Regulation Histones Histone H4 Mice Endocrinology Genes jun Bone cell medicine Animals Orthopedics and Sports Medicine RNA Messenger Osteoblasts Triiodothyronine Dose-Response Relationship Drug biology c-jun Genes fos Cell Differentiation 3T3 Cells Alkaline Phosphatase Molecular biology In vitro Phenotype medicine.anatomical_structure Gene Expression Regulation biology.protein Alkaline phosphatase |
Zdroj: | Calcified Tissue International. 61:404-411 |
ISSN: | 1432-0827 0171-967X |
DOI: | 10.1007/s002239900356 |
Popis: | Thyroid hormones influence growth and differentiation of bone cells. In vivo and in vitro data indicate their importance for development and maintenance of the skeleton. Triiodothyronine (T3) inhibits proliferation and accelerates differentiation of osteoblasts. We studied the regulatory effect of T3 on markers of proliferation as well as on specific markers of the osteoblastic phenotype in cultured MC3T3-E1 cells at different time points. In parallel to the inhibitory effect on proliferation, T3 down-regulated histone H4 mRNA expression. Early genes (c-fos/c-jun) are highly expressed in proliferating cells and are down-regulated when the cells switch to differentiation. When MC3T3-E1 cells are cultured under serum-free conditions, basal c-fos/c-jun expressions are nearly undetectable. Under these conditions, c-fos/c-jun mRNAs can be stimulated by EGF, the effect of which is attenuated to about 46% by T3. In addition, T3 stimulated the expression at the mRNA and protein level of osteocalcin, a marker of mature osteoblasts and alkaline phosphatase activity. All these effects were more pronounced when cells were cultured for more than 6 days. These data indicate that T3 acts as a differentiation factor in osteoblasts by influencing the expression of cell cycle-regulated, of cell growth-regulated, and of phenotypic genes. |
Databáze: | OpenAIRE |
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