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Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node

Lymph nodes (LNs) contain innate-like lymphocytes that survey the subcapsular sinus (SCS) and associated macrophages for pathogen entry. The factors promoting this surveillance behavior have not been defined. Here, we report that IL7R(hi)Ccr6(+) lymphocytes in mouse LNs rapidly produce IL17 upon bac...

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Autores principales: Zhang, Yang, Roth, Theodore L, Gray, Elizabeth E, Chen, Hsin, Rodda, Lauren B, Liang, Yin, Ventura, Patrick, Villeda, Saul, Crocker, Paul R, Cyster, Jason G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017864/
https://www.ncbi.nlm.nih.gov/pubmed/27487469
http://dx.doi.org/10.7554/eLife.18156
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author Zhang, Yang
Roth, Theodore L
Gray, Elizabeth E
Chen, Hsin
Rodda, Lauren B
Liang, Yin
Ventura, Patrick
Villeda, Saul
Crocker, Paul R
Cyster, Jason G
author_facet Zhang, Yang
Roth, Theodore L
Gray, Elizabeth E
Chen, Hsin
Rodda, Lauren B
Liang, Yin
Ventura, Patrick
Villeda, Saul
Crocker, Paul R
Cyster, Jason G
author_sort Zhang, Yang
collection PubMed
description Lymph nodes (LNs) contain innate-like lymphocytes that survey the subcapsular sinus (SCS) and associated macrophages for pathogen entry. The factors promoting this surveillance behavior have not been defined. Here, we report that IL7R(hi)Ccr6(+) lymphocytes in mouse LNs rapidly produce IL17 upon bacterial and fungal challenge. We show that these innate-like lymphocytes are mostly LN resident. Ccr6 is required for their accumulation near the SCS and for efficient IL17 induction. Migration into the SCS intrinsically requires S1pr1, whereas movement from the sinus into the parenchyma involves the integrin LFA1 and its ligand ICAM1. CD169, a sialic acid-binding lectin, helps retain the cells within the sinus, preventing their loss in lymph flow. These findings establish a role for Ccr6 in augmenting innate-like lymphocyte responses to lymph-borne pathogens, and they define requirements for cell movement between parenchyma and SCS in what we speculate is a program of immune surveillance that helps achieve LN barrier immunity. DOI: http://dx.doi.org/10.7554/eLife.18156.001
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spelling pubmed-50178642016-09-12 Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node Zhang, Yang Roth, Theodore L Gray, Elizabeth E Chen, Hsin Rodda, Lauren B Liang, Yin Ventura, Patrick Villeda, Saul Crocker, Paul R Cyster, Jason G eLife Immunology Lymph nodes (LNs) contain innate-like lymphocytes that survey the subcapsular sinus (SCS) and associated macrophages for pathogen entry. The factors promoting this surveillance behavior have not been defined. Here, we report that IL7R(hi)Ccr6(+) lymphocytes in mouse LNs rapidly produce IL17 upon bacterial and fungal challenge. We show that these innate-like lymphocytes are mostly LN resident. Ccr6 is required for their accumulation near the SCS and for efficient IL17 induction. Migration into the SCS intrinsically requires S1pr1, whereas movement from the sinus into the parenchyma involves the integrin LFA1 and its ligand ICAM1. CD169, a sialic acid-binding lectin, helps retain the cells within the sinus, preventing their loss in lymph flow. These findings establish a role for Ccr6 in augmenting innate-like lymphocyte responses to lymph-borne pathogens, and they define requirements for cell movement between parenchyma and SCS in what we speculate is a program of immune surveillance that helps achieve LN barrier immunity. DOI: http://dx.doi.org/10.7554/eLife.18156.001 eLife Sciences Publications, Ltd 2016-08-03 /pmc/articles/PMC5017864/ /pubmed/27487469 http://dx.doi.org/10.7554/eLife.18156 Text en © 2016, Zhang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Immunology
Zhang, Yang
Roth, Theodore L
Gray, Elizabeth E
Chen, Hsin
Rodda, Lauren B
Liang, Yin
Ventura, Patrick
Villeda, Saul
Crocker, Paul R
Cyster, Jason G
Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title_full Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title_fullStr Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title_full_unstemmed Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title_short Migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
title_sort migratory and adhesive cues controlling innate-like lymphocyte surveillance of the pathogen-exposed surface of the lymph node
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5017864/
https://www.ncbi.nlm.nih.gov/pubmed/27487469
http://dx.doi.org/10.7554/eLife.18156
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