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The osteoclastogenic factor of osteoblastic origin has recently been elucidated as a novel Tumor Necrosis Factor (TNF)-ligand family member, termed osteoclast differentiation factor (ODF). Using a semiquantitative RT-PCR approach, we sought to determine the mRNA expression of ODF and its decoy receptor, osteoprotegerin (OPG), in a selection of osteoblastic cell lines and in response to three factors representative of different signal transduction pathways, vitamin D receptor, protein kinase A or gp130. Each osteotropic agent, either 1,25-(OH)2D3, PTH or IL-11, promoted an increase in the ratio of ODF:OPG, with maximal stimulation occurring at 24 h, 4 h, and 8 h, respectively, and furthermore each was shown to act in a dose-dependent manner. This report establishes that osteoblastic cell lines incapable of supporting osteoclast formation have markedly reduced ODF expression and also illustrates the importance of the relative abundance of ODF compared with the levels of OPG for the induction of osteoclastogenesis.
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Nicole J. Horwood
University of East Anglia
Jan Elliott
VA Palo Alto Health Care System
T. John Martin
The Open University
Endocrinology
The University of Melbourne
St Vincent's Hospital
St Vincents Institute of Medical Research
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Horwood et al. (Sun,) studied this question.
synapsesocial.com/papers/6a2394a7b57190d467d34677 — DOI: https://doi.org/10.1210/endo.139.11.6433