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 |
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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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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.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/j.bone.2006.12.064</identifier><identifier>PMID: 17320497</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>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</subject><ispartof>Bone (New York, N.Y.), 2007-05, Vol.40 (5), p.1370-1377</ispartof><rights>Elsevier Inc.</rights><rights>2007 Elsevier Inc.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c635t-3e2b52d3fb1b28a72c98a77f20283e7334770b0db02fffae48d3452f7a21af743</citedby><cites>FETCH-LOGICAL-c635t-3e2b52d3fb1b28a72c98a77f20283e7334770b0db02fffae48d3452f7a21af743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S8756328206009525$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18739948$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17320497$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Characterization of circulating osteoblast lineage cells in humans</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><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.</description><subject>Adult</subject><subject>Age Distribution</subject><subject>Aged</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Biomarkers</subject><subject>Cell Lineage</subject><subject>Cell Separation</subject><subject>Circulating</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunophenotyping</subject><subject>Male</subject><subject>Mesenchymal</subject><subject>Middle Aged</subject><subject>Orthopedics</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>Osteocalcin</subject><subject>Osteocalcin - immunology</subject><subject>Osteocalcin - metabolism</subject><subject>Phenotype</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFu1DAQQC0EotvCD3BAucAty3icxImEKsGKAlIlDsDZcpzxrpesXeykUvl6HO2KAge42LL8ZjzjN4w947DmwJtX-3UfPK0RoFlzXENTPWAr3kpRomzEQ7ZqZd2UAls8Y-cp7QFAdJI_ZmdcCoSqkyv2drPTUZuJovuhJxd8EWxhXDTzmI9-W4Q0UehHnaZidJ70lgpD45gK54vdfNA-PWGPrB4TPT3tF-zr1bsvmw_l9af3HzdvrkvTiHoqBWFf4yBsz3tstUTT5VVaBGwFSSEqKaGHoQe01mqq2kFUNVqpkWsrK3HBLo95b-b-QIMhP0U9qpvoDjreqaCd-vPGu53ahlvFO4S64jnBy1OCGL7PlCZ1cGlpRnsKc1IShGyQ439B3jWSixoyiEfQxJBSJPurGg5qcaT2anGkFkeKo8qOctDz3_u4DzlJycCLE6CT0aON2huX7rlsuOuqNnOvjxzlX791FFUyjryhwUUykxqC-3cdl3-Fm2zY5Re_0R2lfZijzz4VVykHqM_LNC3DBA1AV2MtfgJzScWh</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Eghbali-Fatourechi, Guiti Z</creator><creator>Mödder, Ulrike I.L</creator><creator>Charatcharoenwitthaya, Natthinee</creator><creator>Sanyal, Arunik</creator><creator>Undale, Anita H</creator><creator>Clowes, Jackie A</creator><creator>Tarara, James E</creator><creator>Khosla, Sundeep</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20070501</creationdate><title>Characterization of circulating osteoblast lineage cells in humans</title><author>Eghbali-Fatourechi, Guiti Z ; Mödder, Ulrike I.L ; Charatcharoenwitthaya, Natthinee ; Sanyal, Arunik ; Undale, Anita H ; Clowes, Jackie A ; Tarara, James E ; Khosla, Sundeep</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c635t-3e2b52d3fb1b28a72c98a77f20283e7334770b0db02fffae48d3452f7a21af743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Age Distribution</topic><topic>Aged</topic><topic>Antibodies</topic><topic>Biological and medical sciences</topic><topic>Biomarkers</topic><topic>Cell Lineage</topic><topic>Cell Separation</topic><topic>Circulating</topic><topic>Fundamental and applied biological sciences. 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 & 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). 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.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>17320497</pmid><doi>10.1016/j.bone.2006.12.064</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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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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