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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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Detalles Bibliográficos
Autor principal: Ritchlin, Christopher
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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
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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
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