Experimental models linking dendritic cell lineage, phenotype and function
One of the important issues in dendritic cell (DC) biology today is how DC control the fate of T cells. Our data suggest that an important branch point in determining T cell fate is the decision between deletion and memory. We have previously hypothesized that this binary decision is determined by c...
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Veröffentlicht in: | Immunology and cell biology 2002-10, Vol.80 (5), p.469-476 |
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description | One of the important issues in dendritic cell (DC) biology today is how DC control the fate of T cells. Our data suggest that an important branch point in determining T cell fate is the decision between deletion and memory. We have previously hypothesized that this binary decision is determined by contact with DC derived from lymphoid‐ versus myeloid‐restricted progenitors. However, the false attribution of CD8α expression as a reliable marker of lymphoid origin has underpinned a number of studies in which DC expressing CD8α did not induce deletion, thereby clouding the issue of whether deletion is indeed a function of lymphoid DC. By returning to basics, that is, functional testing of the progeny of lymphoid‐ and myeloid‐restricted progenitors in vivo, we hope to provide clear evidence of the in vivo roles of lymphoid and myeloid DC subsets, independent of assumptions about the surface phenotypes they can assume. |
doi_str_mv | 10.1046/j.1440-1711.2002.01117.x |
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Our data suggest that an important branch point in determining T cell fate is the decision between deletion and memory. We have previously hypothesized that this binary decision is determined by contact with DC derived from lymphoid‐ versus myeloid‐restricted progenitors. However, the false attribution of CD8α expression as a reliable marker of lymphoid origin has underpinned a number of studies in which DC expressing CD8α did not induce deletion, thereby clouding the issue of whether deletion is indeed a function of lymphoid DC. By returning to basics, that is, functional testing of the progeny of lymphoid‐ and myeloid‐restricted progenitors in vivo, we hope to provide clear evidence of the in vivo roles of lymphoid and myeloid DC subsets, independent of assumptions about the surface phenotypes they can assume.</description><identifier>ISSN: 0818-9641</identifier><identifier>EISSN: 1440-1711</identifier><identifier>DOI: 10.1046/j.1440-1711.2002.01117.x</identifier><identifier>PMID: 12225383</identifier><language>eng</language><publisher>United States: Nature Publishing Group</publisher><subject>Animals ; Antigen Presentation - immunology ; Biological Evolution ; CD8 Antigens - analysis ; Cell Lineage ; Clonal Deletion ; dendritic cells ; Dendritic Cells - classification ; Dendritic Cells - immunology ; Dendritic Cells - transplantation ; haemopoietic lineage ; Histocompatibility Antigens Class II - immunology ; Immune Tolerance - immunology ; Immunologic Memory ; Immunophenotyping ; Lymphocytes - cytology ; Lymphocytes - immunology ; Mice ; Mice, Transgenic ; Myeloid Cells - cytology ; Myeloid Cells - immunology ; Spleen - cytology ; Spleen - immunology ; T-Lymphocyte Subsets - cytology ; T-Lymphocyte Subsets - immunology ; tolerance ; transgenic mice ; Vertebrates - immunology</subject><ispartof>Immunology and cell biology, 2002-10, Vol.80 (5), p.469-476</ispartof><rights>2002 Australasian Society for Immunology Inc.</rights><rights>Copyright Nature Publishing Group Oct 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4515-96d849416b4070eaaa9ebd7b122f4961ed2fd1da64f924034ce463b8361e26553</citedby><cites>FETCH-LOGICAL-c4515-96d849416b4070eaaa9ebd7b122f4961ed2fd1da64f924034ce463b8361e26553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1440-1711.2002.01117.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1440-1711.2002.01117.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12225383$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fazekas De St Groth, Barbara</creatorcontrib><creatorcontrib>Smith, Adrian L</creatorcontrib><creatorcontrib>Bosco, Julian</creatorcontrib><creatorcontrib>Sze, Daniel M‐Y</creatorcontrib><creatorcontrib>Power, Carl A</creatorcontrib><creatorcontrib>Austen, Felicity I</creatorcontrib><title>Experimental models linking dendritic cell lineage, phenotype and function</title><title>Immunology and cell biology</title><addtitle>Immunol Cell Biol</addtitle><description>One of the important issues in dendritic cell (DC) biology today is how DC control the fate of T cells. Our data suggest that an important branch point in determining T cell fate is the decision between deletion and memory. We have previously hypothesized that this binary decision is determined by contact with DC derived from lymphoid‐ versus myeloid‐restricted progenitors. However, the false attribution of CD8α expression as a reliable marker of lymphoid origin has underpinned a number of studies in which DC expressing CD8α did not induce deletion, thereby clouding the issue of whether deletion is indeed a function of lymphoid DC. 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Smith, Adrian L ; Bosco, Julian ; Sze, Daniel M‐Y ; Power, Carl A ; Austen, Felicity I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4515-96d849416b4070eaaa9ebd7b122f4961ed2fd1da64f924034ce463b8361e26553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Antigen Presentation - immunology</topic><topic>Biological Evolution</topic><topic>CD8 Antigens - analysis</topic><topic>Cell Lineage</topic><topic>Clonal Deletion</topic><topic>dendritic cells</topic><topic>Dendritic Cells - classification</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - transplantation</topic><topic>haemopoietic lineage</topic><topic>Histocompatibility Antigens Class II - immunology</topic><topic>Immune Tolerance - immunology</topic><topic>Immunologic Memory</topic><topic>Immunophenotyping</topic><topic>Lymphocytes - cytology</topic><topic>Lymphocytes - immunology</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Myeloid Cells - cytology</topic><topic>Myeloid Cells - immunology</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>T-Lymphocyte Subsets - cytology</topic><topic>T-Lymphocyte Subsets - immunology</topic><topic>tolerance</topic><topic>transgenic mice</topic><topic>Vertebrates - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fazekas De St Groth, Barbara</creatorcontrib><creatorcontrib>Smith, Adrian L</creatorcontrib><creatorcontrib>Bosco, Julian</creatorcontrib><creatorcontrib>Sze, Daniel M‐Y</creatorcontrib><creatorcontrib>Power, Carl A</creatorcontrib><creatorcontrib>Austen, Felicity I</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>Health & Medical Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</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>Biological Science Database</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunology and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fazekas De St Groth, Barbara</au><au>Smith, Adrian L</au><au>Bosco, Julian</au><au>Sze, Daniel M‐Y</au><au>Power, Carl A</au><au>Austen, Felicity I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental models linking dendritic cell lineage, phenotype and function</atitle><jtitle>Immunology and cell biology</jtitle><addtitle>Immunol Cell Biol</addtitle><date>2002-10</date><risdate>2002</risdate><volume>80</volume><issue>5</issue><spage>469</spage><epage>476</epage><pages>469-476</pages><issn>0818-9641</issn><eissn>1440-1711</eissn><abstract>One of the important issues in dendritic cell (DC) biology today is how DC control the fate of T cells. Our data suggest that an important branch point in determining T cell fate is the decision between deletion and memory. We have previously hypothesized that this binary decision is determined by contact with DC derived from lymphoid‐ versus myeloid‐restricted progenitors. However, the false attribution of CD8α expression as a reliable marker of lymphoid origin has underpinned a number of studies in which DC expressing CD8α did not induce deletion, thereby clouding the issue of whether deletion is indeed a function of lymphoid DC. 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subjects | Animals Antigen Presentation - immunology Biological Evolution CD8 Antigens - analysis Cell Lineage Clonal Deletion dendritic cells Dendritic Cells - classification Dendritic Cells - immunology Dendritic Cells - transplantation haemopoietic lineage Histocompatibility Antigens Class II - immunology Immune Tolerance - immunology Immunologic Memory Immunophenotyping Lymphocytes - cytology Lymphocytes - immunology Mice Mice, Transgenic Myeloid Cells - cytology Myeloid Cells - immunology Spleen - cytology Spleen - immunology T-Lymphocyte Subsets - cytology T-Lymphocyte Subsets - immunology tolerance transgenic mice Vertebrates - immunology |
title | Experimental models linking dendritic cell lineage, phenotype and function |
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