Loading…
Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line
We have previously shown that xenogeneic stromal cell stimulation of naïve T cells resulted in the generation of a new type of regulatory T (Treg) cell termed HOZOT, which has multifunctional properties and a CD4/CD8 double‐positive phenotype. Even after the establishment of HOZOT, stromal cells can...
Saved in:
Published in: | Immunology and cell biology 2011-02, Vol.89 (2), p.246-254 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183 |
---|---|
cites | cdi_FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183 |
container_end_page | 254 |
container_issue | 2 |
container_start_page | 246 |
container_title | Immunology and cell biology |
container_volume | 89 |
creator | Otani, Takeshi Tsuji‐Takayama, Kazue Okochi, Ayumi Yamamoto, Mayuko Takeuchi, Makoto Yamasaki, Fumiyuki Nakamura, Shuji Kibata, Masayoshi |
description | We have previously shown that xenogeneic stromal cell stimulation of naïve T cells resulted in the generation of a new type of regulatory T (Treg) cell termed HOZOT, which has multifunctional properties and a CD4/CD8 double‐positive phenotype. Even after the establishment of HOZOT, stromal cells can function as an antigen‐presenting cell (APC) by inducing these cells to produce interleukin (IL)‐10. When compared with other stimuli, stromal cells showed an IL‐10‐producing ability comparable to anti‐CD3 antibody (Ab) stimulation, and much greater than dendritic cell (DC) stimulation. Distinct from professional APCs, stromal cells express only major histocompatibility complex (MHC) class I and B7‐1 costimulatory molecules, and not MHC class II or other costimulatory molecules, such as ICOSL (CD275), PD‐L1 (CD274), PD‐L2 (CD273), CD40, OX40L (CD252) and 4‐1BBL (CD137L) in the absence of stimulation. Blocking experiments revealed that, in addition to anti‐H‐2Kd Ab and anti‐human CD8 Ab, anti‐mouse B7‐1 Ab could effectively block IL‐10 production, indicating a key role of the B7‐1/CD28 pathway. Using stromal cells expressing different levels of B7‐1, IL‐10 production correlated with the levels of B7‐1 expression. Distinct from ICOSL or PD‐L1 expressed on DCs (which are regarded as IL‐10‐inducing costimulatory molecules), this study showed that B7‐1 on stromal cells is a key molecule regulating IL‐10 production by multifunctional Treg cells, HOZOT. |
doi_str_mv | 10.1038/icb.2010.87 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_852901951</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4043938441</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183</originalsourceid><addsrcrecordid>eNp9kTFP3TAQx62qqDxop-7IUocOEHp2nNgZyxMtSKA39E1dLD_HQQYnpnasKhtzJ9Z-PT5JHR4wdEAefCf_7n93_iP0kcAxgVJ8sXpzTCFngr9BC8IYFIQT8hYtQBBRNDUju2gvxmsA4FSU79AuhToHvFygPz_G4HvlsDbOxYe7v_iEP9zdE2wjVvjGTDiOtk9OjT5MuPfO6OQM7nzAdhhNcCbd2GGuAHwbfJv0aP2ANxM-W_1crY-ySK4ebZeGx5fcKZirZ711LpwbY2cH8x7tdMpF8-Hp3kfrb6fr5Vlxsfp-vvx6UeiyBl5owkpG8mEsrwG0aTuqNjXvmNJ1VbdaNyWDzlCmq6ZqW0ObCoBSEKDyf5T76PNWNo_7K5k4yt7GeQg1GJ-iFBVtgDQVyeSn_8hrn0JeIUrCRV2JWlRNpg63lA4-xmA6eRtsr8IkCcjZIJkNkrNBUvBMHzxppk1v2hf22ZEMlFvgt3Vmek1Lnl8uT-Y4y_4DMWueIQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1786586859</pqid></control><display><type>article</type><title>Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line</title><source>Wiley</source><creator>Otani, Takeshi ; Tsuji‐Takayama, Kazue ; Okochi, Ayumi ; Yamamoto, Mayuko ; Takeuchi, Makoto ; Yamasaki, Fumiyuki ; Nakamura, Shuji ; Kibata, Masayoshi</creator><creatorcontrib>Otani, Takeshi ; Tsuji‐Takayama, Kazue ; Okochi, Ayumi ; Yamamoto, Mayuko ; Takeuchi, Makoto ; Yamasaki, Fumiyuki ; Nakamura, Shuji ; Kibata, Masayoshi</creatorcontrib><description>We have previously shown that xenogeneic stromal cell stimulation of naïve T cells resulted in the generation of a new type of regulatory T (Treg) cell termed HOZOT, which has multifunctional properties and a CD4/CD8 double‐positive phenotype. Even after the establishment of HOZOT, stromal cells can function as an antigen‐presenting cell (APC) by inducing these cells to produce interleukin (IL)‐10. When compared with other stimuli, stromal cells showed an IL‐10‐producing ability comparable to anti‐CD3 antibody (Ab) stimulation, and much greater than dendritic cell (DC) stimulation. Distinct from professional APCs, stromal cells express only major histocompatibility complex (MHC) class I and B7‐1 costimulatory molecules, and not MHC class II or other costimulatory molecules, such as ICOSL (CD275), PD‐L1 (CD274), PD‐L2 (CD273), CD40, OX40L (CD252) and 4‐1BBL (CD137L) in the absence of stimulation. Blocking experiments revealed that, in addition to anti‐H‐2Kd Ab and anti‐human CD8 Ab, anti‐mouse B7‐1 Ab could effectively block IL‐10 production, indicating a key role of the B7‐1/CD28 pathway. Using stromal cells expressing different levels of B7‐1, IL‐10 production correlated with the levels of B7‐1 expression. Distinct from ICOSL or PD‐L1 expressed on DCs (which are regarded as IL‐10‐inducing costimulatory molecules), this study showed that B7‐1 on stromal cells is a key molecule regulating IL‐10 production by multifunctional Treg cells, HOZOT.</description><identifier>ISSN: 0818-9641</identifier><identifier>EISSN: 1440-1711</identifier><identifier>DOI: 10.1038/icb.2010.87</identifier><identifier>PMID: 20628373</identifier><language>eng</language><publisher>United States: Nature Publishing Group</publisher><subject>Animals ; Antibodies, Monoclonal - biosynthesis ; antigen‐presenting cell ; B7-1 Antigen - immunology ; B7‐1 ; CD8 Antigens - metabolism ; Cell Line ; Dendritic Cells - cytology ; Dendritic Cells - immunology ; Histocompatibility Antigens Class I - immunology ; Humans ; IL‐10 production ; Interleukin-10 - biosynthesis ; Mice ; Phenotype ; regulatory T cell ; stormal cell ; Stromal Cells - cytology ; Stromal Cells - immunology ; T-Lymphocytes, Regulatory - cytology ; T-Lymphocytes, Regulatory - immunology</subject><ispartof>Immunology and cell biology, 2011-02, Vol.89 (2), p.246-254</ispartof><rights>2011 Australasian Society for Immunology Inc.</rights><rights>Copyright Nature Publishing Group Feb 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183</citedby><cites>FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183</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/20628373$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Otani, Takeshi</creatorcontrib><creatorcontrib>Tsuji‐Takayama, Kazue</creatorcontrib><creatorcontrib>Okochi, Ayumi</creatorcontrib><creatorcontrib>Yamamoto, Mayuko</creatorcontrib><creatorcontrib>Takeuchi, Makoto</creatorcontrib><creatorcontrib>Yamasaki, Fumiyuki</creatorcontrib><creatorcontrib>Nakamura, Shuji</creatorcontrib><creatorcontrib>Kibata, Masayoshi</creatorcontrib><title>Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line</title><title>Immunology and cell biology</title><addtitle>Immunol Cell Biol</addtitle><description>We have previously shown that xenogeneic stromal cell stimulation of naïve T cells resulted in the generation of a new type of regulatory T (Treg) cell termed HOZOT, which has multifunctional properties and a CD4/CD8 double‐positive phenotype. Even after the establishment of HOZOT, stromal cells can function as an antigen‐presenting cell (APC) by inducing these cells to produce interleukin (IL)‐10. When compared with other stimuli, stromal cells showed an IL‐10‐producing ability comparable to anti‐CD3 antibody (Ab) stimulation, and much greater than dendritic cell (DC) stimulation. Distinct from professional APCs, stromal cells express only major histocompatibility complex (MHC) class I and B7‐1 costimulatory molecules, and not MHC class II or other costimulatory molecules, such as ICOSL (CD275), PD‐L1 (CD274), PD‐L2 (CD273), CD40, OX40L (CD252) and 4‐1BBL (CD137L) in the absence of stimulation. Blocking experiments revealed that, in addition to anti‐H‐2Kd Ab and anti‐human CD8 Ab, anti‐mouse B7‐1 Ab could effectively block IL‐10 production, indicating a key role of the B7‐1/CD28 pathway. Using stromal cells expressing different levels of B7‐1, IL‐10 production correlated with the levels of B7‐1 expression. Distinct from ICOSL or PD‐L1 expressed on DCs (which are regarded as IL‐10‐inducing costimulatory molecules), this study showed that B7‐1 on stromal cells is a key molecule regulating IL‐10 production by multifunctional Treg cells, HOZOT.</description><subject>Animals</subject><subject>Antibodies, Monoclonal - biosynthesis</subject><subject>antigen‐presenting cell</subject><subject>B7-1 Antigen - immunology</subject><subject>B7‐1</subject><subject>CD8 Antigens - metabolism</subject><subject>Cell Line</subject><subject>Dendritic Cells - cytology</subject><subject>Dendritic Cells - immunology</subject><subject>Histocompatibility Antigens Class I - immunology</subject><subject>Humans</subject><subject>IL‐10 production</subject><subject>Interleukin-10 - biosynthesis</subject><subject>Mice</subject><subject>Phenotype</subject><subject>regulatory T cell</subject><subject>stormal cell</subject><subject>Stromal Cells - cytology</subject><subject>Stromal Cells - immunology</subject><subject>T-Lymphocytes, Regulatory - cytology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><issn>0818-9641</issn><issn>1440-1711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kTFP3TAQx62qqDxop-7IUocOEHp2nNgZyxMtSKA39E1dLD_HQQYnpnasKhtzJ9Z-PT5JHR4wdEAefCf_7n93_iP0kcAxgVJ8sXpzTCFngr9BC8IYFIQT8hYtQBBRNDUju2gvxmsA4FSU79AuhToHvFygPz_G4HvlsDbOxYe7v_iEP9zdE2wjVvjGTDiOtk9OjT5MuPfO6OQM7nzAdhhNcCbd2GGuAHwbfJv0aP2ANxM-W_1crY-ySK4ebZeGx5fcKZirZ711LpwbY2cH8x7tdMpF8-Hp3kfrb6fr5Vlxsfp-vvx6UeiyBl5owkpG8mEsrwG0aTuqNjXvmNJ1VbdaNyWDzlCmq6ZqW0ObCoBSEKDyf5T76PNWNo_7K5k4yt7GeQg1GJ-iFBVtgDQVyeSn_8hrn0JeIUrCRV2JWlRNpg63lA4-xmA6eRtsr8IkCcjZIJkNkrNBUvBMHzxppk1v2hf22ZEMlFvgt3Vmek1Lnl8uT-Y4y_4DMWueIQ</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Otani, Takeshi</creator><creator>Tsuji‐Takayama, Kazue</creator><creator>Okochi, Ayumi</creator><creator>Yamamoto, Mayuko</creator><creator>Takeuchi, Makoto</creator><creator>Yamasaki, Fumiyuki</creator><creator>Nakamura, Shuji</creator><creator>Kibata, Masayoshi</creator><general>Nature Publishing Group</general><general>Blackwell Science 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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>201102</creationdate><title>Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line</title><author>Otani, Takeshi ; Tsuji‐Takayama, Kazue ; Okochi, Ayumi ; Yamamoto, Mayuko ; Takeuchi, Makoto ; Yamasaki, Fumiyuki ; Nakamura, Shuji ; Kibata, Masayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Antibodies, Monoclonal - biosynthesis</topic><topic>antigen‐presenting cell</topic><topic>B7-1 Antigen - immunology</topic><topic>B7‐1</topic><topic>CD8 Antigens - metabolism</topic><topic>Cell Line</topic><topic>Dendritic Cells - cytology</topic><topic>Dendritic Cells - immunology</topic><topic>Histocompatibility Antigens Class I - immunology</topic><topic>Humans</topic><topic>IL‐10 production</topic><topic>Interleukin-10 - biosynthesis</topic><topic>Mice</topic><topic>Phenotype</topic><topic>regulatory T cell</topic><topic>stormal cell</topic><topic>Stromal Cells - cytology</topic><topic>Stromal Cells - immunology</topic><topic>T-Lymphocytes, Regulatory - cytology</topic><topic>T-Lymphocytes, Regulatory - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Otani, Takeshi</creatorcontrib><creatorcontrib>Tsuji‐Takayama, Kazue</creatorcontrib><creatorcontrib>Okochi, Ayumi</creatorcontrib><creatorcontrib>Yamamoto, Mayuko</creatorcontrib><creatorcontrib>Takeuchi, Makoto</creatorcontrib><creatorcontrib>Yamasaki, Fumiyuki</creatorcontrib><creatorcontrib>Nakamura, Shuji</creatorcontrib><creatorcontrib>Kibata, Masayoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Immunology and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Otani, Takeshi</au><au>Tsuji‐Takayama, Kazue</au><au>Okochi, Ayumi</au><au>Yamamoto, Mayuko</au><au>Takeuchi, Makoto</au><au>Yamasaki, Fumiyuki</au><au>Nakamura, Shuji</au><au>Kibata, Masayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line</atitle><jtitle>Immunology and cell biology</jtitle><addtitle>Immunol Cell Biol</addtitle><date>2011-02</date><risdate>2011</risdate><volume>89</volume><issue>2</issue><spage>246</spage><epage>254</epage><pages>246-254</pages><issn>0818-9641</issn><eissn>1440-1711</eissn><abstract>We have previously shown that xenogeneic stromal cell stimulation of naïve T cells resulted in the generation of a new type of regulatory T (Treg) cell termed HOZOT, which has multifunctional properties and a CD4/CD8 double‐positive phenotype. Even after the establishment of HOZOT, stromal cells can function as an antigen‐presenting cell (APC) by inducing these cells to produce interleukin (IL)‐10. When compared with other stimuli, stromal cells showed an IL‐10‐producing ability comparable to anti‐CD3 antibody (Ab) stimulation, and much greater than dendritic cell (DC) stimulation. Distinct from professional APCs, stromal cells express only major histocompatibility complex (MHC) class I and B7‐1 costimulatory molecules, and not MHC class II or other costimulatory molecules, such as ICOSL (CD275), PD‐L1 (CD274), PD‐L2 (CD273), CD40, OX40L (CD252) and 4‐1BBL (CD137L) in the absence of stimulation. Blocking experiments revealed that, in addition to anti‐H‐2Kd Ab and anti‐human CD8 Ab, anti‐mouse B7‐1 Ab could effectively block IL‐10 production, indicating a key role of the B7‐1/CD28 pathway. Using stromal cells expressing different levels of B7‐1, IL‐10 production correlated with the levels of B7‐1 expression. Distinct from ICOSL or PD‐L1 expressed on DCs (which are regarded as IL‐10‐inducing costimulatory molecules), this study showed that B7‐1 on stromal cells is a key molecule regulating IL‐10 production by multifunctional Treg cells, HOZOT.</abstract><cop>United States</cop><pub>Nature Publishing Group</pub><pmid>20628373</pmid><doi>10.1038/icb.2010.87</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0818-9641 |
ispartof | Immunology and cell biology, 2011-02, Vol.89 (2), p.246-254 |
issn | 0818-9641 1440-1711 |
language | eng |
recordid | cdi_proquest_miscellaneous_852901951 |
source | Wiley |
subjects | Animals Antibodies, Monoclonal - biosynthesis antigen‐presenting cell B7-1 Antigen - immunology B7‐1 CD8 Antigens - metabolism Cell Line Dendritic Cells - cytology Dendritic Cells - immunology Histocompatibility Antigens Class I - immunology Humans IL‐10 production Interleukin-10 - biosynthesis Mice Phenotype regulatory T cell stormal cell Stromal Cells - cytology Stromal Cells - immunology T-Lymphocytes, Regulatory - cytology T-Lymphocytes, Regulatory - immunology |
title | Stromal cells’ B7‐1 is a key stimulatory molecule for interleukin‐10 production by HOZOT, a multifunctional regulatory T‐cell line |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T13%3A02%3A42IST&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=Stromal%20cells%E2%80%99%20B7%E2%80%901%20is%20a%20key%20stimulatory%20molecule%20for%20interleukin%E2%80%9010%20production%20by%20HOZOT,%20a%20multifunctional%20regulatory%20T%E2%80%90cell%20line&rft.jtitle=Immunology%20and%20cell%20biology&rft.au=Otani,%20Takeshi&rft.date=2011-02&rft.volume=89&rft.issue=2&rft.spage=246&rft.epage=254&rft.pages=246-254&rft.issn=0818-9641&rft.eissn=1440-1711&rft_id=info:doi/10.1038/icb.2010.87&rft_dat=%3Cproquest_cross%3E4043938441%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3607-c1434141444206029df2ab67f4ac656dcc9340fe24c595dde2950022080a8183%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1786586859&rft_id=info:pmid/20628373&rfr_iscdi=true |