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The quest for a biomarker of circulating osteoclast precursors
Osteoclast precursors arise from the CD14+ CD16- population in controls but details about cell surface marker expression and functional characteristics of these cells is unknown, particularly in patients with inflammatory arthritis. In a recent issue of Arthritis, Research and Therapy, Lari and coll...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714124/ https://www.ncbi.nlm.nih.gov/pubmed/19591635 http://dx.doi.org/10.1186/ar2707 |
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author | Ritchlin, Christopher |
author_facet | Ritchlin, Christopher |
author_sort | Ritchlin, Christopher |
collection | PubMed |
description | Osteoclast precursors arise from the CD14+ CD16- population in controls but details about cell surface marker expression and functional characteristics of these cells is unknown, particularly in patients with inflammatory arthritis. In a recent issue of Arthritis, Research and Therapy, Lari and colleagues found that osteoclasts developed from a proliferative CD14+ CD16- subset in healthy controls. These cells took on the morphology of osteoclasts, expressed mRNA for osteoclast-related genes and excavated pits on bone wafers. These findings provide new insights into monocyte diversity and provide evidence that osteoclast precursors arise from a small proliferating monocyte population in controls. Additional studies are needed in patients with inflammatory arthritis |
format | Text |
id | pubmed-2714124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27141242009-07-22 The quest for a biomarker of circulating osteoclast precursors Ritchlin, Christopher Arthritis Res Ther Editorial Osteoclast precursors arise from the CD14+ CD16- population in controls but details about cell surface marker expression and functional characteristics of these cells is unknown, particularly in patients with inflammatory arthritis. In a recent issue of Arthritis, Research and Therapy, Lari and colleagues found that osteoclasts developed from a proliferative CD14+ CD16- subset in healthy controls. These cells took on the morphology of osteoclasts, expressed mRNA for osteoclast-related genes and excavated pits on bone wafers. These findings provide new insights into monocyte diversity and provide evidence that osteoclast precursors arise from a small proliferating monocyte population in controls. Additional studies are needed in patients with inflammatory arthritis BioMed Central 2009 2009-06-17 /pmc/articles/PMC2714124/ /pubmed/19591635 http://dx.doi.org/10.1186/ar2707 Text en Copyright © 2009 BioMed Central Ltd |
spellingShingle | Editorial Ritchlin, Christopher The quest for a biomarker of circulating osteoclast precursors |
title | The quest for a biomarker of circulating osteoclast precursors |
title_full | The quest for a biomarker of circulating osteoclast precursors |
title_fullStr | The quest for a biomarker of circulating osteoclast precursors |
title_full_unstemmed | The quest for a biomarker of circulating osteoclast precursors |
title_short | The quest for a biomarker of circulating osteoclast precursors |
title_sort | quest for a biomarker of circulating osteoclast precursors |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714124/ https://www.ncbi.nlm.nih.gov/pubmed/19591635 http://dx.doi.org/10.1186/ar2707 |
work_keys_str_mv | AT ritchlinchristopher thequestforabiomarkerofcirculatingosteoclastprecursors AT ritchlinchristopher questforabiomarkerofcirculatingosteoclastprecursors |