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Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes
Although effector CD4(+) T cells readily respond to antigen outside the vasculature, how they respond to intravascular antigens is unknown. Here we show the process of intravascular antigen recognition using intravital multiphoton microscopy of glomeruli. CD4(+) T cells undergo intravascular migrati...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821889/ https://www.ncbi.nlm.nih.gov/pubmed/29467472 http://dx.doi.org/10.1038/s41467-018-03181-4 |
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author | Westhorpe, Clare L. V. Norman, M. Ursula Hall, Pam Snelgrove, Sarah L. Finsterbusch, Michaela Li, Anqi Lo, Camden Tan, Zhe Hao Li, Songhui Nilsson, Susan K. Kitching, A. Richard Hickey, Michael J. |
author_facet | Westhorpe, Clare L. V. Norman, M. Ursula Hall, Pam Snelgrove, Sarah L. Finsterbusch, Michaela Li, Anqi Lo, Camden Tan, Zhe Hao Li, Songhui Nilsson, Susan K. Kitching, A. Richard Hickey, Michael J. |
author_sort | Westhorpe, Clare L. V. |
collection | PubMed |
description | Although effector CD4(+) T cells readily respond to antigen outside the vasculature, how they respond to intravascular antigens is unknown. Here we show the process of intravascular antigen recognition using intravital multiphoton microscopy of glomeruli. CD4(+) T cells undergo intravascular migration within uninflamed glomeruli. Similarly, while MHCII is not expressed by intrinsic glomerular cells, intravascular MHCII-expressing immune cells patrol glomerular capillaries, interacting with CD4(+) T cells. Following intravascular deposition of antigen in glomeruli, effector CD4(+) T-cell responses, including NFAT1 nuclear translocation and decreased migration, are consistent with antigen recognition. Of the MHCII(+) immune cells adherent in glomerular capillaries, only monocytes are retained for prolonged durations. These cells can also induce T-cell proliferation in vitro. Moreover, monocyte depletion reduces CD4(+) T-cell-dependent glomerular inflammation. These findings indicate that MHCII(+) monocytes patrolling the glomerular microvasculature can present intravascular antigen to CD4(+) T cells within glomerular capillaries, leading to antigen-dependent inflammation. |
format | Online Article Text |
id | pubmed-5821889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58218892018-02-23 Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes Westhorpe, Clare L. V. Norman, M. Ursula Hall, Pam Snelgrove, Sarah L. Finsterbusch, Michaela Li, Anqi Lo, Camden Tan, Zhe Hao Li, Songhui Nilsson, Susan K. Kitching, A. Richard Hickey, Michael J. Nat Commun Article Although effector CD4(+) T cells readily respond to antigen outside the vasculature, how they respond to intravascular antigens is unknown. Here we show the process of intravascular antigen recognition using intravital multiphoton microscopy of glomeruli. CD4(+) T cells undergo intravascular migration within uninflamed glomeruli. Similarly, while MHCII is not expressed by intrinsic glomerular cells, intravascular MHCII-expressing immune cells patrol glomerular capillaries, interacting with CD4(+) T cells. Following intravascular deposition of antigen in glomeruli, effector CD4(+) T-cell responses, including NFAT1 nuclear translocation and decreased migration, are consistent with antigen recognition. Of the MHCII(+) immune cells adherent in glomerular capillaries, only monocytes are retained for prolonged durations. These cells can also induce T-cell proliferation in vitro. Moreover, monocyte depletion reduces CD4(+) T-cell-dependent glomerular inflammation. These findings indicate that MHCII(+) monocytes patrolling the glomerular microvasculature can present intravascular antigen to CD4(+) T cells within glomerular capillaries, leading to antigen-dependent inflammation. Nature Publishing Group UK 2018-02-21 /pmc/articles/PMC5821889/ /pubmed/29467472 http://dx.doi.org/10.1038/s41467-018-03181-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Westhorpe, Clare L. V. Norman, M. Ursula Hall, Pam Snelgrove, Sarah L. Finsterbusch, Michaela Li, Anqi Lo, Camden Tan, Zhe Hao Li, Songhui Nilsson, Susan K. Kitching, A. Richard Hickey, Michael J. Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title | Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title_full | Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title_fullStr | Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title_full_unstemmed | Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title_short | Effector CD4(+) T cells recognize intravascular antigen presented by patrolling monocytes |
title_sort | effector cd4(+) t cells recognize intravascular antigen presented by patrolling monocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5821889/ https://www.ncbi.nlm.nih.gov/pubmed/29467472 http://dx.doi.org/10.1038/s41467-018-03181-4 |
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