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Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes
Subcapsular sinus macrophages (SSMs) in lymph nodes are rapidly exposed to antigens arriving in afferent lymph and have a role in their capture and display to B cells. In tissue sections SSMs exhibit long cellular processes and express high amounts of CD169. Here, we show that many of the cells pres...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365896/ https://www.ncbi.nlm.nih.gov/pubmed/22675532 http://dx.doi.org/10.1371/journal.pone.0038258 |
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author | Gray, Elizabeth E. Friend, Sherree Suzuki, Kazuhiro Phan, Tri Giang Cyster, Jason G. |
author_facet | Gray, Elizabeth E. Friend, Sherree Suzuki, Kazuhiro Phan, Tri Giang Cyster, Jason G. |
author_sort | Gray, Elizabeth E. |
collection | PubMed |
description | Subcapsular sinus macrophages (SSMs) in lymph nodes are rapidly exposed to antigens arriving in afferent lymph and have a role in their capture and display to B cells. In tissue sections SSMs exhibit long cellular processes and express high amounts of CD169. Here, we show that many of the cells present in lymph node cell suspensions that stain for CD169 are not macrophages but lymphocytes that have acquired SSM-derived membrane blebs. The CD169 bleb(+) lymphocytes are enriched for IL-17 committed IL-7Rα(hi)CCR6(+) T cells and NK cells. In addition, the CD169 staining detected on small numbers of CD11c(hi) dendritic cells is frequently associated with membrane blebs. Counter intuitively the CD169 bleb(+) lymphocytes are mostly CD4 and CD8 negative whereas many SSMs express CD4. In situ, many IL-7Rα(hi) cells are present at the subcapsular sinus and interfollicular regions and migrate in close association with CD169(+) macrophages. These findings suggest SSMs undergo fragmentation during tissue preparation and release blebs that are acquired by closely associated cells. They also suggest an intimate crosstalk between SSMs and IL-17 committed innate-like lymphocytes that may help provide early protection of the lymph node against lymph-borne invaders. |
format | Online Article Text |
id | pubmed-3365896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33658962012-06-06 Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes Gray, Elizabeth E. Friend, Sherree Suzuki, Kazuhiro Phan, Tri Giang Cyster, Jason G. PLoS One Research Article Subcapsular sinus macrophages (SSMs) in lymph nodes are rapidly exposed to antigens arriving in afferent lymph and have a role in their capture and display to B cells. In tissue sections SSMs exhibit long cellular processes and express high amounts of CD169. Here, we show that many of the cells present in lymph node cell suspensions that stain for CD169 are not macrophages but lymphocytes that have acquired SSM-derived membrane blebs. The CD169 bleb(+) lymphocytes are enriched for IL-17 committed IL-7Rα(hi)CCR6(+) T cells and NK cells. In addition, the CD169 staining detected on small numbers of CD11c(hi) dendritic cells is frequently associated with membrane blebs. Counter intuitively the CD169 bleb(+) lymphocytes are mostly CD4 and CD8 negative whereas many SSMs express CD4. In situ, many IL-7Rα(hi) cells are present at the subcapsular sinus and interfollicular regions and migrate in close association with CD169(+) macrophages. These findings suggest SSMs undergo fragmentation during tissue preparation and release blebs that are acquired by closely associated cells. They also suggest an intimate crosstalk between SSMs and IL-17 committed innate-like lymphocytes that may help provide early protection of the lymph node against lymph-borne invaders. Public Library of Science 2012-06-01 /pmc/articles/PMC3365896/ /pubmed/22675532 http://dx.doi.org/10.1371/journal.pone.0038258 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Gray, Elizabeth E. Friend, Sherree Suzuki, Kazuhiro Phan, Tri Giang Cyster, Jason G. Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title | Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title_full | Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title_fullStr | Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title_full_unstemmed | Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title_short | Subcapsular Sinus Macrophage Fragmentation and CD169(+) Bleb Acquisition by Closely Associated IL-17-Committed Innate-Like Lymphocytes |
title_sort | subcapsular sinus macrophage fragmentation and cd169(+) bleb acquisition by closely associated il-17-committed innate-like lymphocytes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365896/ https://www.ncbi.nlm.nih.gov/pubmed/22675532 http://dx.doi.org/10.1371/journal.pone.0038258 |
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