CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors

Mesenchymal progenitor cells (MPCs) exhibit fibroblast‐like morphology and are multipotent cells capable of differentiating into various mesenchymal tissues. Although MPCs have been found in adult bone marrow and umbilical cord blood, there is still controversy as to whether the MPCs are present in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Stem cells (Dayton, Ohio) Ohio), 2008-10, Vol.26 (10), p.2523-2530
Hauptverfasser: Chiba, Haruki, Ishii, Genicihro, Ito, Ta‐Kashi, Aoyagi, Kazuhiro, Sasaki, Hiroki, Nagai, Kanji, Ochiai, Atsushi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2530
container_issue 10
container_start_page 2523
container_title Stem cells (Dayton, Ohio)
container_volume 26
creator Chiba, Haruki
Ishii, Genicihro
Ito, Ta‐Kashi
Aoyagi, Kazuhiro
Sasaki, Hiroki
Nagai, Kanji
Ochiai, Atsushi
description Mesenchymal progenitor cells (MPCs) exhibit fibroblast‐like morphology and are multipotent cells capable of differentiating into various mesenchymal tissues. Although MPCs have been found in adult bone marrow and umbilical cord blood, there is still controversy as to whether the MPCs are present in adult human blood. To determine whether they are, we cultured mononuclear cells (MNCs) from the pulmonary arterial blood of lung cancer patients. In 94% (29 of 31) of the cases, fibroblasts were expanded ex vivo and were differentiated into an osteogenic lineage or an adipogenic lineage, depending on the specific inducing medium used. These results indicated that pulmonary arterial blood (PA) in the vicinity of lung cancers contains MPCs (PA‐MPCs). The cDNA profiles of PA‐MPCs, MPCs derived from bone marrow (BM‐MPCs), and lung tissue‐derived fibroblasts were clustered with a hierarchical classification algorithm. The expression profiles of PA‐MPCs (three cases) and BM‐MPCs were clearly separated from those of the tissue‐derived fibroblasts, and the profiles of the PA‐MPCs from the two patients were separated from those of the BM‐MPCs. To identify the source of the PA‐MPCs, the MNCs from pulmonary arterial blood were exposed to anti‐CD14, anti‐CD105, anti‐CD3, and anti‐CD20 antibodies. CD105+ MNCs generated MPCs in eight of eight cases (100%), whereas CD14+, CD3+, and CD20+ mononuclear cells generated MPCs in three of five cases (60%), two of five cases (40%), and zero of three cases (0%), respectively. These findings are the first clear proof that the CD105+ MNC fraction in the pulmonary arterial blood of adult lung cancer patients includes MPCs. Disclosure of potential conflicts of interest is found at the end of this article.
doi_str_mv 10.1634/stemcells.2008-0037
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69692741</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69692741</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4973-ca7e244746b1290b85e847eff92a4f5e03e56378e23df57c2db2e8d40ac94f6f3</originalsourceid><addsrcrecordid>eNqNkc1u1DAURi1ERUvhCZCQV4hNWv8nXg5poZWmYiTK2vI4N8XIsYudFM2OR-AZeRISzYjuUFf3Ls73XekehN5QckYVF-dlhMFBCOWMEdJUhPD6GTqhUuhKaNo8n3eiVCWJ1sfoZSnfCaFCNs0LdEwbpbSm_AQ9tBeUyD-_fm9S8aN_ANwuldhHvJnCkKLNO7zKI2RvA_4QUupw6vGqm8KIr6bBRrye4h1ubXSQ8caOHuJY8HV0YeoA30CB6L7thjm9yekOoh9TLq_QUW9DgdeHeYq-fry8ba-q9edP1-1qXTmha145WwMTohZqS5km20ZCI2roe82s6CUQDlLxugHGu17WjnVbBk0niHVa9Krnp-jdvvc-px8TlNEMvixPsxHSVIzSSrNa0Bl8_1-QSiI5l7UkM8r3qMuplAy9uc9-mP9kKDGLGfPPjFnMmMXMnHp7ODBtB-geMwcVM6D3wE8fYPeUTvPl9vKGScb5X2ntoBU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1505335750</pqid></control><display><type>article</type><title>CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Chiba, Haruki ; Ishii, Genicihro ; Ito, Ta‐Kashi ; Aoyagi, Kazuhiro ; Sasaki, Hiroki ; Nagai, Kanji ; Ochiai, Atsushi</creator><creatorcontrib>Chiba, Haruki ; Ishii, Genicihro ; Ito, Ta‐Kashi ; Aoyagi, Kazuhiro ; Sasaki, Hiroki ; Nagai, Kanji ; Ochiai, Atsushi</creatorcontrib><description>Mesenchymal progenitor cells (MPCs) exhibit fibroblast‐like morphology and are multipotent cells capable of differentiating into various mesenchymal tissues. Although MPCs have been found in adult bone marrow and umbilical cord blood, there is still controversy as to whether the MPCs are present in adult human blood. To determine whether they are, we cultured mononuclear cells (MNCs) from the pulmonary arterial blood of lung cancer patients. In 94% (29 of 31) of the cases, fibroblasts were expanded ex vivo and were differentiated into an osteogenic lineage or an adipogenic lineage, depending on the specific inducing medium used. These results indicated that pulmonary arterial blood (PA) in the vicinity of lung cancers contains MPCs (PA‐MPCs). The cDNA profiles of PA‐MPCs, MPCs derived from bone marrow (BM‐MPCs), and lung tissue‐derived fibroblasts were clustered with a hierarchical classification algorithm. The expression profiles of PA‐MPCs (three cases) and BM‐MPCs were clearly separated from those of the tissue‐derived fibroblasts, and the profiles of the PA‐MPCs from the two patients were separated from those of the BM‐MPCs. To identify the source of the PA‐MPCs, the MNCs from pulmonary arterial blood were exposed to anti‐CD14, anti‐CD105, anti‐CD3, and anti‐CD20 antibodies. CD105+ MNCs generated MPCs in eight of eight cases (100%), whereas CD14+, CD3+, and CD20+ mononuclear cells generated MPCs in three of five cases (60%), two of five cases (40%), and zero of three cases (0%), respectively. These findings are the first clear proof that the CD105+ MNC fraction in the pulmonary arterial blood of adult lung cancer patients includes MPCs. Disclosure of potential conflicts of interest is found at the end of this article.</description><identifier>ISSN: 1066-5099</identifier><identifier>EISSN: 1549-4918</identifier><identifier>DOI: 10.1634/stemcells.2008-0037</identifier><identifier>PMID: 18669913</identifier><language>eng</language><publisher>Bristol: John Wiley &amp; Sons, Ltd</publisher><subject>Adipogenesis ; Adult ; Algorithms ; Antigens, CD - metabolism ; Blood Cells - cytology ; Blood Cells - metabolism ; CD105 ; Cell Proliferation ; Cell Separation ; Endoglin ; Fibroblasts - cytology ; Gene Expression Profiling ; Humans ; Lipopolysaccharide Receptors - metabolism ; Lung cancer ; Lung Neoplasms - blood ; Lung Neoplasms - pathology ; Mesenchymal progenitor cell ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - metabolism ; Oligonucleotide Array Sequence Analysis ; Osteogenesis ; Peripheral blood ; Pulmonary Artery - cytology ; Receptors, Cell Surface - metabolism ; RNA, Messenger - genetics ; RNA, Messenger - metabolism</subject><ispartof>Stem cells (Dayton, Ohio), 2008-10, Vol.26 (10), p.2523-2530</ispartof><rights>Copyright © 2008 AlphaMed Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4973-ca7e244746b1290b85e847eff92a4f5e03e56378e23df57c2db2e8d40ac94f6f3</citedby><cites>FETCH-LOGICAL-c4973-ca7e244746b1290b85e847eff92a4f5e03e56378e23df57c2db2e8d40ac94f6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18669913$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiba, Haruki</creatorcontrib><creatorcontrib>Ishii, Genicihro</creatorcontrib><creatorcontrib>Ito, Ta‐Kashi</creatorcontrib><creatorcontrib>Aoyagi, Kazuhiro</creatorcontrib><creatorcontrib>Sasaki, Hiroki</creatorcontrib><creatorcontrib>Nagai, Kanji</creatorcontrib><creatorcontrib>Ochiai, Atsushi</creatorcontrib><title>CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors</title><title>Stem cells (Dayton, Ohio)</title><addtitle>Stem Cells</addtitle><description>Mesenchymal progenitor cells (MPCs) exhibit fibroblast‐like morphology and are multipotent cells capable of differentiating into various mesenchymal tissues. Although MPCs have been found in adult bone marrow and umbilical cord blood, there is still controversy as to whether the MPCs are present in adult human blood. To determine whether they are, we cultured mononuclear cells (MNCs) from the pulmonary arterial blood of lung cancer patients. In 94% (29 of 31) of the cases, fibroblasts were expanded ex vivo and were differentiated into an osteogenic lineage or an adipogenic lineage, depending on the specific inducing medium used. These results indicated that pulmonary arterial blood (PA) in the vicinity of lung cancers contains MPCs (PA‐MPCs). The cDNA profiles of PA‐MPCs, MPCs derived from bone marrow (BM‐MPCs), and lung tissue‐derived fibroblasts were clustered with a hierarchical classification algorithm. The expression profiles of PA‐MPCs (three cases) and BM‐MPCs were clearly separated from those of the tissue‐derived fibroblasts, and the profiles of the PA‐MPCs from the two patients were separated from those of the BM‐MPCs. To identify the source of the PA‐MPCs, the MNCs from pulmonary arterial blood were exposed to anti‐CD14, anti‐CD105, anti‐CD3, and anti‐CD20 antibodies. CD105+ MNCs generated MPCs in eight of eight cases (100%), whereas CD14+, CD3+, and CD20+ mononuclear cells generated MPCs in three of five cases (60%), two of five cases (40%), and zero of three cases (0%), respectively. These findings are the first clear proof that the CD105+ MNC fraction in the pulmonary arterial blood of adult lung cancer patients includes MPCs. Disclosure of potential conflicts of interest is found at the end of this article.</description><subject>Adipogenesis</subject><subject>Adult</subject><subject>Algorithms</subject><subject>Antigens, CD - metabolism</subject><subject>Blood Cells - cytology</subject><subject>Blood Cells - metabolism</subject><subject>CD105</subject><subject>Cell Proliferation</subject><subject>Cell Separation</subject><subject>Endoglin</subject><subject>Fibroblasts - cytology</subject><subject>Gene Expression Profiling</subject><subject>Humans</subject><subject>Lipopolysaccharide Receptors - metabolism</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - blood</subject><subject>Lung Neoplasms - pathology</subject><subject>Mesenchymal progenitor cell</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Oligonucleotide Array Sequence Analysis</subject><subject>Osteogenesis</subject><subject>Peripheral blood</subject><subject>Pulmonary Artery - cytology</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><issn>1066-5099</issn><issn>1549-4918</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURi1ERUvhCZCQV4hNWv8nXg5poZWmYiTK2vI4N8XIsYudFM2OR-AZeRISzYjuUFf3Ls73XekehN5QckYVF-dlhMFBCOWMEdJUhPD6GTqhUuhKaNo8n3eiVCWJ1sfoZSnfCaFCNs0LdEwbpbSm_AQ9tBeUyD-_fm9S8aN_ANwuldhHvJnCkKLNO7zKI2RvA_4QUupw6vGqm8KIr6bBRrye4h1ubXSQ8caOHuJY8HV0YeoA30CB6L7thjm9yekOoh9TLq_QUW9DgdeHeYq-fry8ba-q9edP1-1qXTmha145WwMTohZqS5km20ZCI2roe82s6CUQDlLxugHGu17WjnVbBk0niHVa9Krnp-jdvvc-px8TlNEMvixPsxHSVIzSSrNa0Bl8_1-QSiI5l7UkM8r3qMuplAy9uc9-mP9kKDGLGfPPjFnMmMXMnHp7ODBtB-geMwcVM6D3wE8fYPeUTvPl9vKGScb5X2ntoBU</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Chiba, Haruki</creator><creator>Ishii, Genicihro</creator><creator>Ito, Ta‐Kashi</creator><creator>Aoyagi, Kazuhiro</creator><creator>Sasaki, Hiroki</creator><creator>Nagai, Kanji</creator><creator>Ochiai, Atsushi</creator><general>John Wiley &amp; Sons, Ltd</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200810</creationdate><title>CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors</title><author>Chiba, Haruki ; Ishii, Genicihro ; Ito, Ta‐Kashi ; Aoyagi, Kazuhiro ; Sasaki, Hiroki ; Nagai, Kanji ; Ochiai, Atsushi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4973-ca7e244746b1290b85e847eff92a4f5e03e56378e23df57c2db2e8d40ac94f6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adipogenesis</topic><topic>Adult</topic><topic>Algorithms</topic><topic>Antigens, CD - metabolism</topic><topic>Blood Cells - cytology</topic><topic>Blood Cells - metabolism</topic><topic>CD105</topic><topic>Cell Proliferation</topic><topic>Cell Separation</topic><topic>Endoglin</topic><topic>Fibroblasts - cytology</topic><topic>Gene Expression Profiling</topic><topic>Humans</topic><topic>Lipopolysaccharide Receptors - metabolism</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - blood</topic><topic>Lung Neoplasms - pathology</topic><topic>Mesenchymal progenitor cell</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>Mesenchymal Stromal Cells - metabolism</topic><topic>Oligonucleotide Array Sequence Analysis</topic><topic>Osteogenesis</topic><topic>Peripheral blood</topic><topic>Pulmonary Artery - cytology</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiba, Haruki</creatorcontrib><creatorcontrib>Ishii, Genicihro</creatorcontrib><creatorcontrib>Ito, Ta‐Kashi</creatorcontrib><creatorcontrib>Aoyagi, Kazuhiro</creatorcontrib><creatorcontrib>Sasaki, Hiroki</creatorcontrib><creatorcontrib>Nagai, Kanji</creatorcontrib><creatorcontrib>Ochiai, Atsushi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Stem cells (Dayton, Ohio)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiba, Haruki</au><au>Ishii, Genicihro</au><au>Ito, Ta‐Kashi</au><au>Aoyagi, Kazuhiro</au><au>Sasaki, Hiroki</au><au>Nagai, Kanji</au><au>Ochiai, Atsushi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors</atitle><jtitle>Stem cells (Dayton, Ohio)</jtitle><addtitle>Stem Cells</addtitle><date>2008-10</date><risdate>2008</risdate><volume>26</volume><issue>10</issue><spage>2523</spage><epage>2530</epage><pages>2523-2530</pages><issn>1066-5099</issn><eissn>1549-4918</eissn><abstract>Mesenchymal progenitor cells (MPCs) exhibit fibroblast‐like morphology and are multipotent cells capable of differentiating into various mesenchymal tissues. Although MPCs have been found in adult bone marrow and umbilical cord blood, there is still controversy as to whether the MPCs are present in adult human blood. To determine whether they are, we cultured mononuclear cells (MNCs) from the pulmonary arterial blood of lung cancer patients. In 94% (29 of 31) of the cases, fibroblasts were expanded ex vivo and were differentiated into an osteogenic lineage or an adipogenic lineage, depending on the specific inducing medium used. These results indicated that pulmonary arterial blood (PA) in the vicinity of lung cancers contains MPCs (PA‐MPCs). The cDNA profiles of PA‐MPCs, MPCs derived from bone marrow (BM‐MPCs), and lung tissue‐derived fibroblasts were clustered with a hierarchical classification algorithm. The expression profiles of PA‐MPCs (three cases) and BM‐MPCs were clearly separated from those of the tissue‐derived fibroblasts, and the profiles of the PA‐MPCs from the two patients were separated from those of the BM‐MPCs. To identify the source of the PA‐MPCs, the MNCs from pulmonary arterial blood were exposed to anti‐CD14, anti‐CD105, anti‐CD3, and anti‐CD20 antibodies. CD105+ MNCs generated MPCs in eight of eight cases (100%), whereas CD14+, CD3+, and CD20+ mononuclear cells generated MPCs in three of five cases (60%), two of five cases (40%), and zero of three cases (0%), respectively. These findings are the first clear proof that the CD105+ MNC fraction in the pulmonary arterial blood of adult lung cancer patients includes MPCs. Disclosure of potential conflicts of interest is found at the end of this article.</abstract><cop>Bristol</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>18669913</pmid><doi>10.1634/stemcells.2008-0037</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1066-5099
ispartof Stem cells (Dayton, Ohio), 2008-10, Vol.26 (10), p.2523-2530
issn 1066-5099
1549-4918
language eng
recordid cdi_proquest_miscellaneous_69692741
source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adipogenesis
Adult
Algorithms
Antigens, CD - metabolism
Blood Cells - cytology
Blood Cells - metabolism
CD105
Cell Proliferation
Cell Separation
Endoglin
Fibroblasts - cytology
Gene Expression Profiling
Humans
Lipopolysaccharide Receptors - metabolism
Lung cancer
Lung Neoplasms - blood
Lung Neoplasms - pathology
Mesenchymal progenitor cell
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - metabolism
Oligonucleotide Array Sequence Analysis
Osteogenesis
Peripheral blood
Pulmonary Artery - cytology
Receptors, Cell Surface - metabolism
RNA, Messenger - genetics
RNA, Messenger - metabolism
title CD105‐Positive Cells in Pulmonary Arterial Blood of Adult Human Lung Cancer Patients Include Mesenchymal Progenitors
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T00%3A45%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=CD105%E2%80%90Positive%20Cells%20in%20Pulmonary%20Arterial%20Blood%20of%20Adult%20Human%20Lung%20Cancer%20Patients%20Include%20Mesenchymal%20Progenitors&rft.jtitle=Stem%20cells%20(Dayton,%20Ohio)&rft.au=Chiba,%20Haruki&rft.date=2008-10&rft.volume=26&rft.issue=10&rft.spage=2523&rft.epage=2530&rft.pages=2523-2530&rft.issn=1066-5099&rft.eissn=1549-4918&rft_id=info:doi/10.1634/stemcells.2008-0037&rft_dat=%3Cproquest_cross%3E69692741%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1505335750&rft_id=info:pmid/18669913&rfr_iscdi=true