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The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption

The contribution of osteoclasts to the process of bone loss in inflammatory arthritis has recently been demonstrated. Studies in osteoclast biology have led to the identification of factors responsible for the differentiation and activation of osteoclasts, the most important of which is the receptor...

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Detalles Bibliográficos
Autores principales: Gravallese, Ellen M, Galson, Deborah L, Goldring, Steven R, Auron, Philip E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC128878/
https://www.ncbi.nlm.nih.gov/pubmed/11178122
http://dx.doi.org/10.1186/ar134
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author Gravallese, Ellen M
Galson, Deborah L
Goldring, Steven R
Auron, Philip E
author_facet Gravallese, Ellen M
Galson, Deborah L
Goldring, Steven R
Auron, Philip E
author_sort Gravallese, Ellen M
collection PubMed
description The contribution of osteoclasts to the process of bone loss in inflammatory arthritis has recently been demonstrated. Studies in osteoclast biology have led to the identification of factors responsible for the differentiation and activation of osteoclasts, the most important of which is the receptor activator of NF-κB ligand/osteoclast differentiation factor (RANKL/ODF), a tumor necrosis factor (TNF)-like protein. The RANKL/ODF receptor, receptor activator of NF-κB (RANK), is a TNF-receptor family member present on both osteoclast precursors and mature osteoclasts. Like other TNF-family receptors and the IL-1 receptor, RANK mediates its signal transduction via TNF receptor-associated factor (TRAF) proteins, suggesting that the signaling pathways activated by RANK and other inflammatory cytokines involved in osteoclast differentiation and activation are interconnected.
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spelling pubmed-1288782002-10-28 The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption Gravallese, Ellen M Galson, Deborah L Goldring, Steven R Auron, Philip E Arthritis Res Review The contribution of osteoclasts to the process of bone loss in inflammatory arthritis has recently been demonstrated. Studies in osteoclast biology have led to the identification of factors responsible for the differentiation and activation of osteoclasts, the most important of which is the receptor activator of NF-κB ligand/osteoclast differentiation factor (RANKL/ODF), a tumor necrosis factor (TNF)-like protein. The RANKL/ODF receptor, receptor activator of NF-κB (RANK), is a TNF-receptor family member present on both osteoclast precursors and mature osteoclasts. Like other TNF-family receptors and the IL-1 receptor, RANK mediates its signal transduction via TNF receptor-associated factor (TRAF) proteins, suggesting that the signaling pathways activated by RANK and other inflammatory cytokines involved in osteoclast differentiation and activation are interconnected. BioMed Central 2001 2000-11-02 /pmc/articles/PMC128878/ /pubmed/11178122 http://dx.doi.org/10.1186/ar134 Text en Copyright © 2000 BioMed Central Ltd on behalf of the copyright holders
spellingShingle Review
Gravallese, Ellen M
Galson, Deborah L
Goldring, Steven R
Auron, Philip E
The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title_full The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title_fullStr The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title_full_unstemmed The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title_short The role of TNF-receptor family members and other TRAF-dependent receptors in bone resorption
title_sort role of tnf-receptor family members and other traf-dependent receptors in bone resorption
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC128878/
https://www.ncbi.nlm.nih.gov/pubmed/11178122
http://dx.doi.org/10.1186/ar134
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