Two lymph nodes draining the mouse liver are the preferential site of DC migration and T cell activation
Background & Aims Lymph nodes (LNs) play a critical role in host defence against pathogens. In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central...
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Veröffentlicht in: | Journal of hepatology 2012-08, Vol.57 (2), p.352-358 |
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description | Background & Aims Lymph nodes (LNs) play a critical role in host defence against pathogens. In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central importance to allow accurate characterization of immune responses to pathogens infecting the liver. It is also important for exploring immune responses in hepatic tumour models, and mechanisms underlying the relative tolerogenic properties of the liver. In this study, we used both anatomical and immunological approaches to identify the LN(s) draining the mouse liver. Methods Evans Blue and purified dendritic cells were directly injected into the hepatic parenchyma. Results Using Evans Blue, we identified three LNs adjacent to the liver that stained with the dye within the first 5 min, which we termed portal, coeliac, and first mesenteric LNs. We also provide evidence that dendritic cells (DCs) injected under the liver capsule preferentially migrate to the coeliac and portal nodes, leading to local activation of antigen-specific naïve CD8 and CD4 T cells, suggesting this is a route of lymphatic drainage from the liver. Consistent with this result, cell-associated antigen injected under the liver capsule was also cross-presented to CD8 T cells in these nodes. Conclusions These results suggest for the first time that the coeliac and portal nodes are the main LNs draining the liver, and that DCs exiting the liver can elicit primary T cell activation within these lymph nodes; first mesenteric nodes play a secondary role. We propose this nomenclature to be used as common designations for the observed structures. |
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In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central importance to allow accurate characterization of immune responses to pathogens infecting the liver. It is also important for exploring immune responses in hepatic tumour models, and mechanisms underlying the relative tolerogenic properties of the liver. In this study, we used both anatomical and immunological approaches to identify the LN(s) draining the mouse liver. Methods Evans Blue and purified dendritic cells were directly injected into the hepatic parenchyma. Results Using Evans Blue, we identified three LNs adjacent to the liver that stained with the dye within the first 5 min, which we termed portal, coeliac, and first mesenteric LNs. We also provide evidence that dendritic cells (DCs) injected under the liver capsule preferentially migrate to the coeliac and portal nodes, leading to local activation of antigen-specific naïve CD8 and CD4 T cells, suggesting this is a route of lymphatic drainage from the liver. Consistent with this result, cell-associated antigen injected under the liver capsule was also cross-presented to CD8 T cells in these nodes. Conclusions These results suggest for the first time that the coeliac and portal nodes are the main LNs draining the liver, and that DCs exiting the liver can elicit primary T cell activation within these lymph nodes; first mesenteric nodes play a secondary role. We propose this nomenclature to be used as common designations for the observed structures.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2012.03.023</identifier><identifier>PMID: 22542491</identifier><identifier>CODEN: JOHEEC</identifier><language>eng</language><publisher>Kidlington: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Cell Movement ; Dendritic cells ; Dendritic Cells - cytology ; Dendritic Cells - physiology ; Draining lymph nodes ; Gastroenterology and Hepatology ; Gastroenterology. Liver. Pancreas. Abdomen ; Liver ; Liver - immunology ; Lymph Nodes - immunology ; Lymphocyte Activation ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; T cells ; T-Lymphocytes - immunology ; Transgenic mice</subject><ispartof>Journal of hepatology, 2012-08, Vol.57 (2), p.352-358</ispartof><rights>European Association for the Study of the Liver</rights><rights>2012 European Association for the Study of the Liver</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-4484c2efcf86512917ea04c6dc0a52a062be06bedab601d2adcf7c5e2cbb62c43</citedby><cites>FETCH-LOGICAL-c441t-4484c2efcf86512917ea04c6dc0a52a062be06bedab601d2adcf7c5e2cbb62c43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jhep.2012.03.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26143710$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22542491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Barbier, Louise</creatorcontrib><creatorcontrib>Tay, Szun Szun</creatorcontrib><creatorcontrib>McGuffog, Claire</creatorcontrib><creatorcontrib>Triccas, James A</creatorcontrib><creatorcontrib>McCaughan, Geoffrey W</creatorcontrib><creatorcontrib>Bowen, David G</creatorcontrib><creatorcontrib>Bertolino, Patrick</creatorcontrib><title>Two lymph nodes draining the mouse liver are the preferential site of DC migration and T cell activation</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Background & Aims Lymph nodes (LNs) play a critical role in host defence against pathogens. In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central importance to allow accurate characterization of immune responses to pathogens infecting the liver. It is also important for exploring immune responses in hepatic tumour models, and mechanisms underlying the relative tolerogenic properties of the liver. In this study, we used both anatomical and immunological approaches to identify the LN(s) draining the mouse liver. Methods Evans Blue and purified dendritic cells were directly injected into the hepatic parenchyma. Results Using Evans Blue, we identified three LNs adjacent to the liver that stained with the dye within the first 5 min, which we termed portal, coeliac, and first mesenteric LNs. We also provide evidence that dendritic cells (DCs) injected under the liver capsule preferentially migrate to the coeliac and portal nodes, leading to local activation of antigen-specific naïve CD8 and CD4 T cells, suggesting this is a route of lymphatic drainage from the liver. Consistent with this result, cell-associated antigen injected under the liver capsule was also cross-presented to CD8 T cells in these nodes. Conclusions These results suggest for the first time that the coeliac and portal nodes are the main LNs draining the liver, and that DCs exiting the liver can elicit primary T cell activation within these lymph nodes; first mesenteric nodes play a secondary role. We propose this nomenclature to be used as common designations for the observed structures.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Movement</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - cytology</subject><subject>Dendritic Cells - physiology</subject><subject>Draining lymph nodes</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Liver</subject><subject>Liver - immunology</subject><subject>Lymph Nodes - immunology</subject><subject>Lymphocyte Activation</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>T cells</subject><subject>T-Lymphocytes - immunology</subject><subject>Transgenic mice</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kk2P0zAQhi0EYsvCH-CAfEHikjB2XCeVENKqfEorcaCcLceebB0SO9hpUf89zraAxIGTpdHzjmcem5DnDEoGTL7uy36PU8mB8RKqEnj1gKyYBChACvaQrDLUFA2vmyvyJKUeACrYiMfkivO14GLDVmS_-xnocBqnPfXBYqI2auedv6PzHukYDgnp4I4YqY54X5sidhjRz04PNLkZaejouy0d3V3Uswueam_pjhocBqrN7I731afkUaeHhM8u5zX59uH9bvupuP3y8fP25rYwQrC5EKIRhmNnukauGd-wGjUII60BveYaJG8RZItWtxKY5dqarjZr5KZtJTeiuiavzn2nGH4cMM1qdGmZRXvM2ygGXDZSAK8zys-oiSGlvJaaoht1PGVILYZVrxbDajGsoFLZcA69uPQ_tCPaP5HfSjPw8gLoZPTQRe2NS385yURVM8jcmzOH2cbRYVTJOPQGrYtoZmWD-_8cb_-JmyE_XL7xO54w9eEQffasmEo5o74uf2H5CoxD3r0R1S9Xnq8V</recordid><startdate>20120801</startdate><enddate>20120801</enddate><creator>Barbier, Louise</creator><creator>Tay, Szun Szun</creator><creator>McGuffog, Claire</creator><creator>Triccas, James A</creator><creator>McCaughan, Geoffrey W</creator><creator>Bowen, David G</creator><creator>Bertolino, Patrick</creator><general>Elsevier B.V</general><general>Elsevier</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></search><sort><creationdate>20120801</creationdate><title>Two lymph nodes draining the mouse liver are the preferential site of DC migration and T cell activation</title><author>Barbier, Louise ; Tay, Szun Szun ; McGuffog, Claire ; Triccas, James A ; McCaughan, Geoffrey W ; Bowen, David G ; Bertolino, Patrick</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-4484c2efcf86512917ea04c6dc0a52a062be06bedab601d2adcf7c5e2cbb62c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Movement</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - cytology</topic><topic>Dendritic Cells - physiology</topic><topic>Draining lymph nodes</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Liver</topic><topic>Liver - immunology</topic><topic>Lymph Nodes - immunology</topic><topic>Lymphocyte Activation</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>T cells</topic><topic>T-Lymphocytes - immunology</topic><topic>Transgenic mice</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barbier, Louise</creatorcontrib><creatorcontrib>Tay, Szun Szun</creatorcontrib><creatorcontrib>McGuffog, Claire</creatorcontrib><creatorcontrib>Triccas, James A</creatorcontrib><creatorcontrib>McCaughan, Geoffrey W</creatorcontrib><creatorcontrib>Bowen, David G</creatorcontrib><creatorcontrib>Bertolino, Patrick</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><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barbier, Louise</au><au>Tay, Szun Szun</au><au>McGuffog, Claire</au><au>Triccas, James A</au><au>McCaughan, Geoffrey W</au><au>Bowen, David G</au><au>Bertolino, Patrick</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two lymph nodes draining the mouse liver are the preferential site of DC migration and T cell activation</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2012-08-01</date><risdate>2012</risdate><volume>57</volume><issue>2</issue><spage>352</spage><epage>358</epage><pages>352-358</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><coden>JOHEEC</coden><abstract>Background & Aims Lymph nodes (LNs) play a critical role in host defence against pathogens. In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central importance to allow accurate characterization of immune responses to pathogens infecting the liver. It is also important for exploring immune responses in hepatic tumour models, and mechanisms underlying the relative tolerogenic properties of the liver. In this study, we used both anatomical and immunological approaches to identify the LN(s) draining the mouse liver. Methods Evans Blue and purified dendritic cells were directly injected into the hepatic parenchyma. Results Using Evans Blue, we identified three LNs adjacent to the liver that stained with the dye within the first 5 min, which we termed portal, coeliac, and first mesenteric LNs. We also provide evidence that dendritic cells (DCs) injected under the liver capsule preferentially migrate to the coeliac and portal nodes, leading to local activation of antigen-specific naïve CD8 and CD4 T cells, suggesting this is a route of lymphatic drainage from the liver. Consistent with this result, cell-associated antigen injected under the liver capsule was also cross-presented to CD8 T cells in these nodes. Conclusions These results suggest for the first time that the coeliac and portal nodes are the main LNs draining the liver, and that DCs exiting the liver can elicit primary T cell activation within these lymph nodes; first mesenteric nodes play a secondary role. We propose this nomenclature to be used as common designations for the observed structures.</abstract><cop>Kidlington</cop><pub>Elsevier B.V</pub><pmid>22542491</pmid><doi>10.1016/j.jhep.2012.03.023</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Movement Dendritic cells Dendritic Cells - cytology Dendritic Cells - physiology Draining lymph nodes Gastroenterology and Hepatology Gastroenterology. Liver. Pancreas. Abdomen Liver Liver - immunology Lymph Nodes - immunology Lymphocyte Activation Medical sciences Mice Mice, Inbred BALB C Mice, Inbred C57BL T cells T-Lymphocytes - immunology Transgenic mice |
title | Two lymph nodes draining the mouse liver are the preferential site of DC migration and T cell activation |
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