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        <title>Article Comments - 'The Quest for a Biomarker of Circulating Osteoclast Precursors'</title>
        <link>http://arthritis-research.com/content/11/3/113/comments</link>
        <description>The latest comments on the article 'The Quest for a Biomarker of Circulating Osteoclast Precursors'</description>
        <dc:date>2009-07-22T14:30:34Z</dc:date>
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        <title>Response to   Editorial by C Ritchlin...</title>
        <link>http://arthritis-research.com/content/11/3/113/comments#362641</link>
        <description>&lt;p&gt;We agree with Dr. Ritchlin that our in vitro demonstration that human osteoclast precursors are within the proliferative monocyte subpopulation must be interpreted with caution; we also support his comments that the importance of the proliferative subset in rheumatoid and psoriatic arthritis should be examined.  As a point of clarification,  the presence and surface phenotyping of this immature proliferative subset in the blood of many donors, as well as the suggestion of its possible relevance to inflammatory/autoimmune conditions, have been reported in a number of previous publications from our laboratory [1-5].  Also, those interested are referred to a recent publication where human osteoclasts could be generated, and potentially in large numbers, from a precursor population derived in turn from hemopoietic stem cells [6]. &lt;br/&gt; &lt;br/&gt;Dr Ritchlin also raises important questions as to whether the proliferative monocyte subpopulation expresses higher cell surface levels of c-Fms to account for the increased proliferative capacity and whether it expresses a unique surface marker(s).  We have not been able to observe any differential expression of c-Fms and no unique surface marker has yet been found, although there is evidence that the subpopulation has altered expression of certain myeloid markers compared with other monocyte populations [5].  As Dr. Ritchlin states, the quest for such a marker(s) on osteoclast precursors should continue so that they can be better characterized. &lt;br/&gt; &lt;br/&gt;1.	Cheung DL, Hamilton JA: Regulation of human monocyte DNA synthesis by colony-stimulating factors, cytokines, and cyclic adenosine monophosphate. Blood 1992, 79(8):1972-1981. &lt;br/&gt;2.	Finnin M, Hamilton JA, Moss ST: Characterization of a CSF-induced proliferating subpopulation of human peripheral blood monocytes by surface marker expression and cytokine production. J Leukoc Biol 1999, 66(6):953-960. &lt;br/&gt;3.	Finnin M, Hamilton JA, Moss ST: Direct comparison of the effects of CSF-1 (M-CSF) and GM-CSF on human monocyte DNA synthesis and CSF receptor expression. J Interferon Cytokine Res 1999, 19(4):417-423. &lt;br/&gt;4.	Moss ST, Hamilton JA: Proliferation of a subpopulation of human peripheral blood monocytes in the presence of colony stimulating factors may contribute to the inflammatory process in diseases such as rheumatoid arthritis. Immunobiology 2000, 202(1):18-25. &lt;br/&gt;5.	Clanchy FI, Holloway AC, Lari R, Cameron PU, Hamilton JA: Detection and properties of the human proliferative monocyte subpopulation. J Leukoc Biol 2006, 79(4):757-766. &lt;br/&gt;6.	Way KJ, Dinh H, Keene MR, White KE, Clanchy FI, Lusby P, Roiniotis J, Cook AD, Cassady AI, Curtis DJ et al: The generation and properties of human macrophage populations from hemopoietic stem cells. J Leukoc Biol 2009, 85(5):766-778.&lt;/p&gt;</description>
                <dc:creator>John Hamilton</dc:creator>
                <dc:date>2009-07-22T14:30:34Z</dc:date>
        <prism:references>http://arthritis-research.com/content/11/3/113</prism:references>
        <prism:person>Ritchlin</prism:person>
        <prism:publicationName>Arthritis Research &amp; Therapy</prism:publicationName>
        <prism:volume>11</prism:volume>
        <prism:startingPage>113</prism:startingPage>
        <prism:publicationDate>Wed Jun 17 00:00:00 BST 2009</prism:publicationDate>
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