Osteotropic agents regulate the expression of osteoclast differentiation factor and osteoprotegerin in osteoblastic stromal cells
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 recep...
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Veröffentlicht in: | Endocrinology (Philadelphia) 1998-11, Vol.139 (11), p.4743-4746 |
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creator | Horwood, N J Elliott, J Martin, T J Gillespie, M T |
description | 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. |
doi_str_mv | 10.1210/en.139.11.4743 |
format | Article |
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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.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Calcitriol - pharmacology</subject><subject>Carrier Proteins</subject><subject>Cells, Cultured</subject><subject>Cyclic AMP-Dependent Protein Kinases - physiology</subject><subject>Cytokines - biosynthesis</subject><subject>glycoprotein gp130</subject><subject>Glycoproteins - pharmacology</subject><subject>Interleukin-11 - pharmacology</subject><subject>Membrane Glycoproteins - biosynthesis</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Osteoblasts - drug effects</subject><subject>osteoclast differentiation factor</subject><subject>Osteoclasts - drug effects</subject><subject>Osteoclasts - metabolism</subject><subject>Osteoprotegerin</subject><subject>Parathyroid Hormone - pharmacology</subject><subject>RANK Ligand</subject><subject>Receptor Activator of Nuclear Factor-kappa B</subject><subject>Receptors, Calcitriol - physiology</subject><subject>Receptors, Cytoplasmic and Nuclear</subject><subject>Receptors, Tumor Necrosis Factor</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Signal Transduction - drug effects</subject><subject>Space life sciences</subject><subject>Stromal Cells - drug effects</subject><issn>0013-7227</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUEtLxDAQzkFZ19WrNyEnb61JkzbpURZfsLAXPZdJOlkrfZmkoEf_ua3uXRgYZuZ7MYRccZbyjLNb7FMuypTzVCopTsiaMS4SlWXqjJyH8D6PUkqxIqtSlVJqvSbf-xBxiH4YG0vhgH0M1ONhaiEijW9I8XP0GEIz9HRwdFjQtoUQad04h34mNBCXqwMbB0-hr_9Qox8iHtA3PZ3rd2UW4uwTZr8OWmqxbcMFOXXQBrw89g15fbh_2T4lu_3j8_Zul1ihdUyksJnLrJa2AAHMGZehqRkYVSqBAMzkRmY5K0pnCm6cFqiQoRAMclBlLjbk5k93DvYxYYhV14QlAfQ4TKFS83e05tm_QK5EwQu-KF4fgZPpsK5G33Tgv6rjc8UP-yB-Rw</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>Horwood, N J</creator><creator>Elliott, J</creator><creator>Martin, T J</creator><creator>Gillespie, M T</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>19981101</creationdate><title>Osteotropic agents regulate the expression of osteoclast differentiation factor and osteoprotegerin in osteoblastic stromal cells</title><author>Horwood, N J ; Elliott, J ; Martin, T J ; Gillespie, M T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c388t-43c2f2c84c6a3a0fbf2ebd0ab7973eaa0b5b425069fb61bf83e7e0e330a5a7953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Calcitriol - pharmacology</topic><topic>Carrier Proteins</topic><topic>Cells, Cultured</topic><topic>Cyclic AMP-Dependent Protein Kinases - physiology</topic><topic>Cytokines - biosynthesis</topic><topic>glycoprotein gp130</topic><topic>Glycoproteins - pharmacology</topic><topic>Interleukin-11 - pharmacology</topic><topic>Membrane Glycoproteins - biosynthesis</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Osteoblasts - drug effects</topic><topic>osteoclast differentiation factor</topic><topic>Osteoclasts - drug effects</topic><topic>Osteoclasts - metabolism</topic><topic>Osteoprotegerin</topic><topic>Parathyroid Hormone - pharmacology</topic><topic>RANK Ligand</topic><topic>Receptor Activator of Nuclear Factor-kappa B</topic><topic>Receptors, Calcitriol - physiology</topic><topic>Receptors, Cytoplasmic and Nuclear</topic><topic>Receptors, Tumor Necrosis Factor</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Signal Transduction - drug effects</topic><topic>Space life sciences</topic><topic>Stromal Cells - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horwood, N J</creatorcontrib><creatorcontrib>Elliott, J</creatorcontrib><creatorcontrib>Martin, T J</creatorcontrib><creatorcontrib>Gillespie, M T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horwood, N J</au><au>Elliott, J</au><au>Martin, T J</au><au>Gillespie, M T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteotropic agents regulate the expression of osteoclast differentiation factor and osteoprotegerin in osteoblastic stromal cells</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>1998-11-01</date><risdate>1998</risdate><volume>139</volume><issue>11</issue><spage>4743</spage><epage>4746</epage><pages>4743-4746</pages><issn>0013-7227</issn><abstract>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.</abstract><cop>United States</cop><pmid>9794488</pmid><doi>10.1210/en.139.11.4743</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Newborn Calcitriol - pharmacology Carrier Proteins Cells, Cultured Cyclic AMP-Dependent Protein Kinases - physiology Cytokines - biosynthesis glycoprotein gp130 Glycoproteins - pharmacology Interleukin-11 - pharmacology Membrane Glycoproteins - biosynthesis Mice Mice, Inbred C57BL Osteoblasts - drug effects osteoclast differentiation factor Osteoclasts - drug effects Osteoclasts - metabolism Osteoprotegerin Parathyroid Hormone - pharmacology RANK Ligand Receptor Activator of Nuclear Factor-kappa B Receptors, Calcitriol - physiology Receptors, Cytoplasmic and Nuclear Receptors, Tumor Necrosis Factor Reverse Transcriptase Polymerase Chain Reaction Signal Transduction - drug effects Space life sciences Stromal Cells - drug effects |
title | Osteotropic agents regulate the expression of osteoclast differentiation factor and osteoprotegerin in osteoblastic stromal cells |
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