Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input
Intrathymic deletion of immature thymocytes that express self-reactive TCR specificities is essential in the generation of self tolerance. Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue-restric...
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Veröffentlicht in: | European journal of immunology 2008-04, Vol.38 (4), p.942-947 |
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creator | White, Andrea J Withers, David R Parnell, Sonia M Scott, Hamish S Finke, Daniela Lane, Peter J.L Jenkinson, Eric J Anderson, Graham |
description | Intrathymic deletion of immature thymocytes that express self-reactive TCR specificities is essential in the generation of self tolerance. Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue-restricted antigens to ensure tolerance to peripheral tissues. Here, we have analysed the cellular and molecular requirements for the initial appearance of Aire⁺ mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis of thymic ontogeny shows that the emergence of embryonic Aire⁺ mTEC occurs prior to the appearance of mature thymocytes, and depends upon lymphoid tissue inducer cells expressing retinoic acid receptor-related orphan receptor γ. In the adult thymus, we show that Aire⁺ mTEC develop in the absence of thymocyte positive and negative selection and CD40 signalling, but are present at reduced frequency. Collectively these data support a model where the initial differentiation of Aire⁺ mTEC involves receptor activator of NF-κB (RANK)-RANKL interactions with lymphoid tissue inducer cells, with subsequent mTEC turnover and/or survival involving CD40-mediated signalling following interactions with mature CD4⁺ thymocytes that express CD40L. |
doi_str_mv | 10.1002/eji.200738052 |
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Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue-restricted antigens to ensure tolerance to peripheral tissues. Here, we have analysed the cellular and molecular requirements for the initial appearance of Aire⁺ mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis of thymic ontogeny shows that the emergence of embryonic Aire⁺ mTEC occurs prior to the appearance of mature thymocytes, and depends upon lymphoid tissue inducer cells expressing retinoic acid receptor-related orphan receptor γ. In the adult thymus, we show that Aire⁺ mTEC develop in the absence of thymocyte positive and negative selection and CD40 signalling, but are present at reduced frequency. Collectively these data support a model where the initial differentiation of Aire⁺ mTEC involves receptor activator of NF-κB (RANK)-RANKL interactions with lymphoid tissue inducer cells, with subsequent mTEC turnover and/or survival involving CD40-mediated signalling following interactions with mature CD4⁺ thymocytes that express CD40L.</description><identifier>ISSN: 0014-2980</identifier><identifier>EISSN: 1521-4141</identifier><identifier>DOI: 10.1002/eji.200738052</identifier><identifier>PMID: 18350550</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>AIRE Protein ; Animals ; CD40 Antigens - immunology ; CD40 Ligand - immunology ; Cell differentiation ; Cell Differentiation - immunology ; Epithelial Cells - cytology ; Epithelial Cells - immunology ; Epithelial Cells - metabolism ; Lymphoid organs ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Thymus ; Thymus Gland - cytology ; Thymus Gland - immunology ; Thymus Gland - metabolism ; Transcription Factors - metabolism</subject><ispartof>European journal of immunology, 2008-04, Vol.38 (4), p.942-947</ispartof><rights>Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. 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Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue-restricted antigens to ensure tolerance to peripheral tissues. Here, we have analysed the cellular and molecular requirements for the initial appearance of Aire⁺ mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis of thymic ontogeny shows that the emergence of embryonic Aire⁺ mTEC occurs prior to the appearance of mature thymocytes, and depends upon lymphoid tissue inducer cells expressing retinoic acid receptor-related orphan receptor γ. In the adult thymus, we show that Aire⁺ mTEC develop in the absence of thymocyte positive and negative selection and CD40 signalling, but are present at reduced frequency. Collectively these data support a model where the initial differentiation of Aire⁺ mTEC involves receptor activator of NF-κB (RANK)-RANKL interactions with lymphoid tissue inducer cells, with subsequent mTEC turnover and/or survival involving CD40-mediated signalling following interactions with mature CD4⁺ thymocytes that express CD40L.</description><subject>AIRE Protein</subject><subject>Animals</subject><subject>CD40 Antigens - immunology</subject><subject>CD40 Ligand - immunology</subject><subject>Cell differentiation</subject><subject>Cell Differentiation - immunology</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - immunology</subject><subject>Epithelial Cells - metabolism</subject><subject>Lymphoid organs</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Thymus</subject><subject>Thymus Gland - cytology</subject><subject>Thymus Gland - immunology</subject><subject>Thymus Gland - metabolism</subject><subject>Transcription Factors - metabolism</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtOxDAQRS0EguVR0kIqusDYjo1dIrS8hEQB1JadnYCR8yBOFvbv8bIroKKyNHPukecSckjhlAKwM3zzpwzgnCsQbINMqGA0L2hBN8kEgBY50wp2yG6MbwCgpdDbZIcqLkAImJDFI76P2Azehqx7tRFj5ptseMVshnMMbVenZdZW2YXvMcfPrscYffOS1TgbQ7D9IsGL2pcZdj7FwlJUYghLz7wN8yTycfBNOXyPxxRJm24c9slWZUPEg_W7R56vpk-XN_n9w_Xt5cV9XhZSsVy7wmoxc85WKNBxjU5IXilnJVrJnUNw2nKhCqFnJUqmpFSgSlnxxIqC75GTlbfr23RqHEzt4_IrtsF2jEbq1KP8BvMVWPZtjD1Wput9nS40FMyya5O6Nj9dJ_5oLR5dauOXXpebgPMV8OEDLv63mend7V_18SpZ2dbYl95H8_zIgHIApSTXjH8BamSW5w</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>White, Andrea J</creator><creator>Withers, David R</creator><creator>Parnell, Sonia M</creator><creator>Scott, Hamish S</creator><creator>Finke, Daniela</creator><creator>Lane, Peter J.L</creator><creator>Jenkinson, Eric J</creator><creator>Anderson, Graham</creator><general>Wiley-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</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>7X8</scope></search><sort><creationdate>200804</creationdate><title>Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input</title><author>White, Andrea J ; Withers, David R ; Parnell, Sonia M ; Scott, Hamish S ; Finke, Daniela ; Lane, Peter J.L ; Jenkinson, Eric J ; Anderson, Graham</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4682-9b4a95dbbafe5eb39eb563f8ba6ea63bbe0b9a358459dce62866808c6f339e543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>AIRE Protein</topic><topic>Animals</topic><topic>CD40 Antigens - immunology</topic><topic>CD40 Ligand - immunology</topic><topic>Cell differentiation</topic><topic>Cell Differentiation - immunology</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - immunology</topic><topic>Epithelial Cells - metabolism</topic><topic>Lymphoid organs</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Thymus</topic><topic>Thymus Gland - cytology</topic><topic>Thymus Gland - immunology</topic><topic>Thymus Gland - metabolism</topic><topic>Transcription Factors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>White, Andrea J</creatorcontrib><creatorcontrib>Withers, David R</creatorcontrib><creatorcontrib>Parnell, Sonia M</creatorcontrib><creatorcontrib>Scott, Hamish S</creatorcontrib><creatorcontrib>Finke, Daniela</creatorcontrib><creatorcontrib>Lane, Peter J.L</creatorcontrib><creatorcontrib>Jenkinson, Eric J</creatorcontrib><creatorcontrib>Anderson, Graham</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>White, Andrea J</au><au>Withers, David R</au><au>Parnell, Sonia M</au><au>Scott, Hamish S</au><au>Finke, Daniela</au><au>Lane, Peter J.L</au><au>Jenkinson, Eric J</au><au>Anderson, Graham</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>2008-04</date><risdate>2008</risdate><volume>38</volume><issue>4</issue><spage>942</spage><epage>947</epage><pages>942-947</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>Intrathymic deletion of immature thymocytes that express self-reactive TCR specificities is essential in the generation of self tolerance. Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue-restricted antigens to ensure tolerance to peripheral tissues. Here, we have analysed the cellular and molecular requirements for the initial appearance of Aire⁺ mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis of thymic ontogeny shows that the emergence of embryonic Aire⁺ mTEC occurs prior to the appearance of mature thymocytes, and depends upon lymphoid tissue inducer cells expressing retinoic acid receptor-related orphan receptor γ. In the adult thymus, we show that Aire⁺ mTEC develop in the absence of thymocyte positive and negative selection and CD40 signalling, but are present at reduced frequency. Collectively these data support a model where the initial differentiation of Aire⁺ mTEC involves receptor activator of NF-κB (RANK)-RANKL interactions with lymphoid tissue inducer cells, with subsequent mTEC turnover and/or survival involving CD40-mediated signalling following interactions with mature CD4⁺ thymocytes that express CD40L.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>18350550</pmid><doi>10.1002/eji.200738052</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AIRE Protein Animals CD40 Antigens - immunology CD40 Ligand - immunology Cell differentiation Cell Differentiation - immunology Epithelial Cells - cytology Epithelial Cells - immunology Epithelial Cells - metabolism Lymphoid organs Mice Mice, Inbred C57BL Mice, Knockout Thymus Thymus Gland - cytology Thymus Gland - immunology Thymus Gland - metabolism Transcription Factors - metabolism |
title | Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input |
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