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CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response

CD4(+) T cell help to CD8(+) T cell responses requires that CD4(+) and CD8(+) T cells interact with the same antigen presenting dendritic cell (Ag(+)DC), but it remains controversial whether helper signals are delivered indirectly through a licensed DC and/or involve direct CD4(+)/CD8(+) T cell cont...

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Autores principales: Barinov, Aleksandr, Galgano, Alessia, Krenn, Gerald, Tanchot, Corinne, Vasseur, Florence, Rocha, Benedita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501581/
https://www.ncbi.nlm.nih.gov/pubmed/28686740
http://dx.doi.org/10.1371/journal.pone.0180644
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author Barinov, Aleksandr
Galgano, Alessia
Krenn, Gerald
Tanchot, Corinne
Vasseur, Florence
Rocha, Benedita
author_facet Barinov, Aleksandr
Galgano, Alessia
Krenn, Gerald
Tanchot, Corinne
Vasseur, Florence
Rocha, Benedita
author_sort Barinov, Aleksandr
collection PubMed
description CD4(+) T cell help to CD8(+) T cell responses requires that CD4(+) and CD8(+) T cells interact with the same antigen presenting dendritic cell (Ag(+)DC), but it remains controversial whether helper signals are delivered indirectly through a licensed DC and/or involve direct CD4(+)/CD8(+) T cell contacts and/or the formation of ternary complexes. We here describe the first in vivo imaging of the intact spleen, aiming to evaluate the first interactions between antigen-specific CD4(+), CD8(+) T cells and Ag(+)DCs. We show that in contrast to CD4(+) T cells which form transient contacts with Ag(+)DC, CD8(+) T cells form immediate stable contacts and activate the Ag(+)DC, acquire fragments of the DC membranes by trogocytosis, leading to their acquisition of some of the DC properties. They express MHC class II, and become able to present the specific Marilyn peptide to naïve Marilyn CD4(+) T cells, inducing their extensive division. In vivo, these CD8(+) T cells form direct stable contacts with motile naïve CD4(+) T cells, recruiting them to Ag(+)DC binding and to the formation of ternary complexes, where CD4(+) and CD8(+) T cells interact with the DC and with one another. The presence of CD8(+) T cells during in vivo immune responses leads to the early activation and up-regulation of multiple functions by CD4(+) T lymphocytes. Thus, while CD4(+) T cell help is important to CD8(+) T cell responses, CD8(+) T cells can interact directly with naïve CD4(+) T cells impacting their recruitment and differentiation.
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spelling pubmed-55015812017-07-25 CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response Barinov, Aleksandr Galgano, Alessia Krenn, Gerald Tanchot, Corinne Vasseur, Florence Rocha, Benedita PLoS One Research Article CD4(+) T cell help to CD8(+) T cell responses requires that CD4(+) and CD8(+) T cells interact with the same antigen presenting dendritic cell (Ag(+)DC), but it remains controversial whether helper signals are delivered indirectly through a licensed DC and/or involve direct CD4(+)/CD8(+) T cell contacts and/or the formation of ternary complexes. We here describe the first in vivo imaging of the intact spleen, aiming to evaluate the first interactions between antigen-specific CD4(+), CD8(+) T cells and Ag(+)DCs. We show that in contrast to CD4(+) T cells which form transient contacts with Ag(+)DC, CD8(+) T cells form immediate stable contacts and activate the Ag(+)DC, acquire fragments of the DC membranes by trogocytosis, leading to their acquisition of some of the DC properties. They express MHC class II, and become able to present the specific Marilyn peptide to naïve Marilyn CD4(+) T cells, inducing their extensive division. In vivo, these CD8(+) T cells form direct stable contacts with motile naïve CD4(+) T cells, recruiting them to Ag(+)DC binding and to the formation of ternary complexes, where CD4(+) and CD8(+) T cells interact with the DC and with one another. The presence of CD8(+) T cells during in vivo immune responses leads to the early activation and up-regulation of multiple functions by CD4(+) T lymphocytes. Thus, while CD4(+) T cell help is important to CD8(+) T cell responses, CD8(+) T cells can interact directly with naïve CD4(+) T cells impacting their recruitment and differentiation. Public Library of Science 2017-07-07 /pmc/articles/PMC5501581/ /pubmed/28686740 http://dx.doi.org/10.1371/journal.pone.0180644 Text en © 2017 Barinov et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Barinov, Aleksandr
Galgano, Alessia
Krenn, Gerald
Tanchot, Corinne
Vasseur, Florence
Rocha, Benedita
CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title_full CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title_fullStr CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title_full_unstemmed CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title_short CD4/CD8/Dendritic cell complexes in the spleen: CD8(+) T cells can directly bind CD4(+) T cells and modulate their response
title_sort cd4/cd8/dendritic cell complexes in the spleen: cd8(+) t cells can directly bind cd4(+) t cells and modulate their response
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501581/
https://www.ncbi.nlm.nih.gov/pubmed/28686740
http://dx.doi.org/10.1371/journal.pone.0180644
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