Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens
Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident...
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Veröffentlicht in: | Journal of the American Society of Nephrology 2013-04, Vol.24 (4), p.543-549 |
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creator | GOTTSCHALK, Catherine DAMUZZO, Vera GOTOT, Janine KROCZEK, Richard A YAGITA, Hideo MURPHY, Kenneth M KNOLLE, Percy A LUDWIG-PORTUGALL, Isis KURTS, Christian |
description | Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. In summary, these results clarify how the kidney/renal lymph node system tolerizes the immune system against circulating innocuous antigens. |
doi_str_mv | 10.1681/ASN.2012101022 |
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Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. In summary, these results clarify how the kidney/renal lymph node system tolerizes the immune system against circulating innocuous antigens.</description><identifier>ISSN: 1046-6673</identifier><identifier>EISSN: 1533-3450</identifier><identifier>DOI: 10.1681/ASN.2012101022</identifier><identifier>PMID: 23411785</identifier><identifier>CODEN: JASNEU</identifier><language>eng</language><publisher>Washington, DC: American Society of Nephrology</publisher><subject>Animals ; Antigens - blood ; Antigens - immunology ; Basic-Leucine Zipper Transcription Factors - genetics ; Basic-Leucine Zipper Transcription Factors - metabolism ; Biological and medical sciences ; Brief Communications ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Immune Tolerance - immunology ; Kidney - immunology ; Kidney - metabolism ; Lymph Nodes - immunology ; Lymph Nodes - metabolism ; Medical sciences ; Mice ; Mice, Mutant Strains ; Nephrology. 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Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. In summary, these results clarify how the kidney/renal lymph node system tolerizes the immune system against circulating innocuous antigens.</description><subject>Animals</subject><subject>Antigens - blood</subject><subject>Antigens - immunology</subject><subject>Basic-Leucine Zipper Transcription Factors - genetics</subject><subject>Basic-Leucine Zipper Transcription Factors - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brief Communications</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Immune Tolerance - immunology</subject><subject>Kidney - immunology</subject><subject>Kidney - metabolism</subject><subject>Lymph Nodes - immunology</subject><subject>Lymph Nodes - metabolism</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Mutant Strains</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Programmed Cell Death 1 Receptor - immunology</subject><subject>Programmed Cell Death 1 Receptor - metabolism</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>T-Lymphocytes, Cytotoxic - metabolism</subject><issn>1046-6673</issn><issn>1533-3450</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUFvGyEQhVHVqkncXnusuFTKZV0GWFgukRwnaSNZqdSmZ4RZsKnWrANspPz7EMVN2tOMNB9vhvcQ-gRkDqKDr4tfN3NKgAIBQukbdAwtYw3jLXlbe8JFI4RkR-gk5z-EQEulfI-OKOMAsmuPkTs3xbPmwu1d7F0s-KLWFEqweOmGIeMQcdk6_NNFM-DVw26_xTdj7_B17Cfr8O04uGRi7czGhJgLXoZkp8GUEDd4EUvYuJg_oHfeDNl9PNQZ-n11ebv83qx-fLteLlaN5ZSURtB1a71QRnVeefBWtlJAay1bK9ExJhkoA4oJ0ikl-851yghuOfieK8V7NkNnz7r7ab1zva0fSmbQ-xR2Jj3o0QT9_ySGrd6M97pKKuC0CpweBNJ4N7lc9C5kW40w0Y1T1sAolYySavIMzZ9Rm8ack_Mva4Dop2x0zUa_ZlMffP73uBf8bxgV-HIATLZm8E--hvzKSeh4C5Q9AoOTlo4</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>GOTTSCHALK, Catherine</creator><creator>DAMUZZO, Vera</creator><creator>GOTOT, Janine</creator><creator>KROCZEK, Richard A</creator><creator>YAGITA, Hideo</creator><creator>MURPHY, Kenneth M</creator><creator>KNOLLE, Percy A</creator><creator>LUDWIG-PORTUGALL, Isis</creator><creator>KURTS, Christian</creator><general>American Society of Nephrology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130401</creationdate><title>Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens</title><author>GOTTSCHALK, Catherine ; DAMUZZO, Vera ; GOTOT, Janine ; KROCZEK, Richard A ; YAGITA, Hideo ; MURPHY, Kenneth M ; KNOLLE, Percy A ; LUDWIG-PORTUGALL, Isis ; KURTS, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-62b5cf69a98f9f1fc757615cc3b968337319a193608997d8e89a64c41fd4994d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Antigens - blood</topic><topic>Antigens - immunology</topic><topic>Basic-Leucine Zipper Transcription Factors - genetics</topic><topic>Basic-Leucine Zipper Transcription Factors - metabolism</topic><topic>Biological and medical sciences</topic><topic>Brief Communications</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Immune Tolerance - immunology</topic><topic>Kidney - immunology</topic><topic>Kidney - metabolism</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - metabolism</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Mutant Strains</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Programmed Cell Death 1 Receptor - immunology</topic><topic>Programmed Cell Death 1 Receptor - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>T-Lymphocytes, Cytotoxic - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GOTTSCHALK, Catherine</creatorcontrib><creatorcontrib>DAMUZZO, Vera</creatorcontrib><creatorcontrib>GOTOT, Janine</creatorcontrib><creatorcontrib>KROCZEK, Richard A</creatorcontrib><creatorcontrib>YAGITA, Hideo</creatorcontrib><creatorcontrib>MURPHY, Kenneth M</creatorcontrib><creatorcontrib>KNOLLE, Percy A</creatorcontrib><creatorcontrib>LUDWIG-PORTUGALL, Isis</creatorcontrib><creatorcontrib>KURTS, Christian</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Society of Nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GOTTSCHALK, Catherine</au><au>DAMUZZO, Vera</au><au>GOTOT, Janine</au><au>KROCZEK, Richard A</au><au>YAGITA, Hideo</au><au>MURPHY, Kenneth M</au><au>KNOLLE, Percy A</au><au>LUDWIG-PORTUGALL, Isis</au><au>KURTS, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens</atitle><jtitle>Journal of the American Society of Nephrology</jtitle><addtitle>J Am Soc Nephrol</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>24</volume><issue>4</issue><spage>543</spage><epage>549</epage><pages>543-549</pages><issn>1046-6673</issn><eissn>1533-3450</eissn><coden>JASNEU</coden><abstract>Although the spleen is a major site where immune tolerance to circulating innocuous antigens occurs, the kidney also contributes. Circulating antigens smaller than albumin are constitutively filtered and concentrated in the kidney and reach the renal lymph node by lymphatic drainage, where resident dendritic cells (DCs) capture them and induce tolerance of specific cytotoxic T cells through unknown mechanisms. Here, we found that the coinhibitory cell surface receptor programmed death 1 (PD-1) on cytotoxic T cells mediates to their tolerance. Renal lymph node DCs of the CD8(+) XCR1(+) subset, which depend on the transcription factor Batf3, expressed the PD-1 cognate ligand PD-L1. Batf3-dependent DCs in the renal lymph node presented antigen that had been concentrated in the kidney and used PD-L1 to induce apoptosis of cytotoxic T cells. In contrast, T cell tolerance in the spleen was independent of PD-1, PD-L1, and Batf3. 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subjects | Animals Antigens - blood Antigens - immunology Basic-Leucine Zipper Transcription Factors - genetics Basic-Leucine Zipper Transcription Factors - metabolism Biological and medical sciences Brief Communications Dendritic Cells - immunology Dendritic Cells - metabolism Immune Tolerance - immunology Kidney - immunology Kidney - metabolism Lymph Nodes - immunology Lymph Nodes - metabolism Medical sciences Mice Mice, Mutant Strains Nephrology. Urinary tract diseases Programmed Cell Death 1 Receptor - immunology Programmed Cell Death 1 Receptor - metabolism Repressor Proteins - genetics Repressor Proteins - metabolism T-Lymphocytes, Cytotoxic - immunology T-Lymphocytes, Cytotoxic - metabolism |
title | Batf3-Dependent Dendritic Cells in the Renal Lymph Node Induce Tolerance against Circulating Antigens |
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