Characterization of circulating osteoblast lineage cells in humans

Abstract We recently identified circulating osteoblastic cells using antibodies to osteocalcin (OCN) or alkaline phosphatase (AP). We now provide a more detailed characterization of these cells. Specifically, we demonstrate that 46% of OCN positive (OCNpos ) cells express AP, and 37% also express th...

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Veröffentlicht in:Bone (New York, N.Y.) N.Y.), 2007-05, Vol.40 (5), p.1370-1377
Hauptverfasser: Eghbali-Fatourechi, Guiti Z, Mödder, Ulrike I.L, Charatcharoenwitthaya, Natthinee, Sanyal, Arunik, Undale, Anita H, Clowes, Jackie A, Tarara, James E, Khosla, Sundeep
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container_end_page 1377
container_issue 5
container_start_page 1370
container_title Bone (New York, N.Y.)
container_volume 40
creator Eghbali-Fatourechi, Guiti Z
Mödder, Ulrike I.L
Charatcharoenwitthaya, Natthinee
Sanyal, Arunik
Undale, Anita H
Clowes, Jackie A
Tarara, James E
Khosla, Sundeep
description Abstract We recently identified circulating osteoblastic cells using antibodies to osteocalcin (OCN) or alkaline phosphatase (AP). We now provide a more detailed characterization of these cells. Specifically, we demonstrate that 46% of OCN positive (OCNpos ) cells express AP, and 37% also express the hematopoietic/endothelial marker CD34. Using two different anti-OCN antibodies and forward/side light scatter characteristics by flow cytometry, we find that OCNpos cells consist of two distinct populations: one population exhibits low forward/side scatter, consistent with a small cell phenotype with low granularity, and a second population has higher forward/side scatter (larger and more granular cell). The smaller, low granularity population also co-expresses CD34, whereas the larger, more granular cells are CD34 negative. Using samples from 26 male subjects aged 28 to 68 years, we demonstrate that the concentration of circulating OCNpos cells increases as a function of age ( R = 0.59, P = 0.002). By contrast, CD34pos cells tend to decrease with age ( R = − 0.31, P = 0.18); as a consequence, the ratio of OCNpos :CD34pos cells also increase significantly with age ( R = 0.54, P = 0.022). These findings suggest significant overlap between circulating cells expressing OCN and those expressing the hematopoietic/endothelial marker CD34. Further studies are needed to define the precise role of circulating OCNpos cells not only in bone remodeling but rather also potentially in the response to vascular injury.
doi_str_mv 10.1016/j.bone.2006.12.064
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Psychology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunophenotyping</topic><topic>Male</topic><topic>Mesenchymal</topic><topic>Middle Aged</topic><topic>Orthopedics</topic><topic>Osteoblasts - cytology</topic><topic>Osteoblasts - metabolism</topic><topic>Osteocalcin</topic><topic>Osteocalcin - immunology</topic><topic>Osteocalcin - metabolism</topic><topic>Phenotype</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eghbali-Fatourechi, Guiti Z</creatorcontrib><creatorcontrib>Mödder, Ulrike I.L</creatorcontrib><creatorcontrib>Charatcharoenwitthaya, Natthinee</creatorcontrib><creatorcontrib>Sanyal, Arunik</creatorcontrib><creatorcontrib>Undale, Anita H</creatorcontrib><creatorcontrib>Clowes, Jackie A</creatorcontrib><creatorcontrib>Tarara, James E</creatorcontrib><creatorcontrib>Khosla, Sundeep</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eghbali-Fatourechi, Guiti Z</au><au>Mödder, Ulrike I.L</au><au>Charatcharoenwitthaya, Natthinee</au><au>Sanyal, Arunik</au><au>Undale, Anita H</au><au>Clowes, Jackie A</au><au>Tarara, James E</au><au>Khosla, Sundeep</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of circulating osteoblast lineage cells in humans</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>2007-05-01</date><risdate>2007</risdate><volume>40</volume><issue>5</issue><spage>1370</spage><epage>1377</epage><pages>1370-1377</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>Abstract We recently identified circulating osteoblastic cells using antibodies to osteocalcin (OCN) or alkaline phosphatase (AP). 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ispartof Bone (New York, N.Y.), 2007-05, Vol.40 (5), p.1370-1377
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Age Distribution
Aged
Antibodies
Biological and medical sciences
Biomarkers
Cell Lineage
Cell Separation
Circulating
Fundamental and applied biological sciences. Psychology
Humans
Immunohistochemistry
Immunophenotyping
Male
Mesenchymal
Middle Aged
Orthopedics
Osteoblasts - cytology
Osteoblasts - metabolism
Osteocalcin
Osteocalcin - immunology
Osteocalcin - metabolism
Phenotype
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Characterization of circulating osteoblast lineage cells in humans
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