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Body barrier surveillance by epidermal gammadelta TCR
The surveillance of body barriers relies on resident T cells whose repertoires are biased toward particular γδ T cell receptor lineages according to location. These γδ TCRs were shown to recognize stress-emergent ligands. Using intravital dynamics-immunosignal correlative microscopy, we report that...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288780/ https://www.ncbi.nlm.nih.gov/pubmed/22327568 http://dx.doi.org/10.1038/ni.2240 |
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author | Chodaczek, Grzegorz Papanna, Veena Zal, M. Anna Zal, Tomasz |
author_facet | Chodaczek, Grzegorz Papanna, Veena Zal, M. Anna Zal, Tomasz |
author_sort | Chodaczek, Grzegorz |
collection | PubMed |
description | The surveillance of body barriers relies on resident T cells whose repertoires are biased toward particular γδ T cell receptor lineages according to location. These γδ TCRs were shown to recognize stress-emergent ligands. Using intravital dynamics-immunosignal correlative microscopy, we report that epidermal T cell-expressed Vγ5 TCRs were constitutively clustered and functionally activated in vivo at steady-state, forming bona-fide immunological synapses that polarized and anchored T cell projections at squamous keratinocyte tight junctions. This synaptogenesis depended on TCR variable domains, Lck and αE(CD103)β7-integrin, but not the γδ lineage or NKG2D. In response to tissue stress, TCR-proximal signals did not increase significantly but underwent stress mode-dependent re-localization. Thus, the γδ TCR orchestrates barrier surveillance pro-actively, presumably by recognizing steady-state-expressed tissue ligands. |
format | Online Article Text |
id | pubmed-3288780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
spelling | pubmed-32887802012-09-01 Body barrier surveillance by epidermal gammadelta TCR Chodaczek, Grzegorz Papanna, Veena Zal, M. Anna Zal, Tomasz Nat Immunol Article The surveillance of body barriers relies on resident T cells whose repertoires are biased toward particular γδ T cell receptor lineages according to location. These γδ TCRs were shown to recognize stress-emergent ligands. Using intravital dynamics-immunosignal correlative microscopy, we report that epidermal T cell-expressed Vγ5 TCRs were constitutively clustered and functionally activated in vivo at steady-state, forming bona-fide immunological synapses that polarized and anchored T cell projections at squamous keratinocyte tight junctions. This synaptogenesis depended on TCR variable domains, Lck and αE(CD103)β7-integrin, but not the γδ lineage or NKG2D. In response to tissue stress, TCR-proximal signals did not increase significantly but underwent stress mode-dependent re-localization. Thus, the γδ TCR orchestrates barrier surveillance pro-actively, presumably by recognizing steady-state-expressed tissue ligands. 2012-02-12 /pmc/articles/PMC3288780/ /pubmed/22327568 http://dx.doi.org/10.1038/ni.2240 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Chodaczek, Grzegorz Papanna, Veena Zal, M. Anna Zal, Tomasz Body barrier surveillance by epidermal gammadelta TCR |
title | Body barrier surveillance by epidermal gammadelta TCR |
title_full | Body barrier surveillance by epidermal gammadelta TCR |
title_fullStr | Body barrier surveillance by epidermal gammadelta TCR |
title_full_unstemmed | Body barrier surveillance by epidermal gammadelta TCR |
title_short | Body barrier surveillance by epidermal gammadelta TCR |
title_sort | body barrier surveillance by epidermal gammadelta tcr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288780/ https://www.ncbi.nlm.nih.gov/pubmed/22327568 http://dx.doi.org/10.1038/ni.2240 |
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