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Identification of a novel antigen cross-presenting cell type in spleen

Antigen-presenting cells (APC), like dendritic cells (DC), are essential for T-cell activation, leading to immunity or tolerance. Multiple DC subsets each play a unique role in the immune response. Here, a novel splenic dendritic-like APC has been characterized in mice that has immune function and c...

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Autores principales: Tan, Jonathan K H, Quah, Ben J C, Griffiths, Kristin L, Periasamy, Pravin, Hey, Ying-Ying, O’Neill, Helen C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822631/
https://www.ncbi.nlm.nih.gov/pubmed/20477902
http://dx.doi.org/10.1111/j.1582-4934.2010.01089.x
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author Tan, Jonathan K H
Quah, Ben J C
Griffiths, Kristin L
Periasamy, Pravin
Hey, Ying-Ying
O’Neill, Helen C
author_facet Tan, Jonathan K H
Quah, Ben J C
Griffiths, Kristin L
Periasamy, Pravin
Hey, Ying-Ying
O’Neill, Helen C
author_sort Tan, Jonathan K H
collection PubMed
description Antigen-presenting cells (APC), like dendritic cells (DC), are essential for T-cell activation, leading to immunity or tolerance. Multiple DC subsets each play a unique role in the immune response. Here, a novel splenic dendritic-like APC has been characterized in mice that has immune function and cell surface phenotype distinct from other, described DC subsets. These were identified as a cell type continuously produced in spleen long-term cultures (LTC) and have an in vivo equivalent cell type in mice, namely ‘L-DC’. This study characterizes LTC-DC in terms of marker phenotype and function, and compares them with L-DC and other known splenic DC and myeloid subsets. L-DC display a myeloid dendritic-like phenotype equivalent to LTC-DC as CD11c(lo)CD11b(hi)MHC-II(−)CD8α(−) cells, distinct by high accessibility and endocytic capacity for blood-borne antigen. Both LTC-DC and L-DC have strong antigen cross-presentation ability leading to strong activation of CD8(+) T cells, particularly after exposure to lipopolysaccharide. However, they have weak ability to stimulate CD4(+) T cells in antigen-specific responses. Evidence is presented here for a novel DC type produced by in vitro haematopoiesis which has distinct antigen-presenting potential and reflects a DC subset present also in vivo in spleen.
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spelling pubmed-38226312015-04-06 Identification of a novel antigen cross-presenting cell type in spleen Tan, Jonathan K H Quah, Ben J C Griffiths, Kristin L Periasamy, Pravin Hey, Ying-Ying O’Neill, Helen C J Cell Mol Med Articles Antigen-presenting cells (APC), like dendritic cells (DC), are essential for T-cell activation, leading to immunity or tolerance. Multiple DC subsets each play a unique role in the immune response. Here, a novel splenic dendritic-like APC has been characterized in mice that has immune function and cell surface phenotype distinct from other, described DC subsets. These were identified as a cell type continuously produced in spleen long-term cultures (LTC) and have an in vivo equivalent cell type in mice, namely ‘L-DC’. This study characterizes LTC-DC in terms of marker phenotype and function, and compares them with L-DC and other known splenic DC and myeloid subsets. L-DC display a myeloid dendritic-like phenotype equivalent to LTC-DC as CD11c(lo)CD11b(hi)MHC-II(−)CD8α(−) cells, distinct by high accessibility and endocytic capacity for blood-borne antigen. Both LTC-DC and L-DC have strong antigen cross-presentation ability leading to strong activation of CD8(+) T cells, particularly after exposure to lipopolysaccharide. However, they have weak ability to stimulate CD4(+) T cells in antigen-specific responses. Evidence is presented here for a novel DC type produced by in vitro haematopoiesis which has distinct antigen-presenting potential and reflects a DC subset present also in vivo in spleen. Blackwell Publishing Ltd 2011-05 2010-05-14 /pmc/articles/PMC3822631/ /pubmed/20477902 http://dx.doi.org/10.1111/j.1582-4934.2010.01089.x Text en © 2011 The Authors Journal of Cellular and Molecular Medicine © 2011 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Tan, Jonathan K H
Quah, Ben J C
Griffiths, Kristin L
Periasamy, Pravin
Hey, Ying-Ying
O’Neill, Helen C
Identification of a novel antigen cross-presenting cell type in spleen
title Identification of a novel antigen cross-presenting cell type in spleen
title_full Identification of a novel antigen cross-presenting cell type in spleen
title_fullStr Identification of a novel antigen cross-presenting cell type in spleen
title_full_unstemmed Identification of a novel antigen cross-presenting cell type in spleen
title_short Identification of a novel antigen cross-presenting cell type in spleen
title_sort identification of a novel antigen cross-presenting cell type in spleen
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822631/
https://www.ncbi.nlm.nih.gov/pubmed/20477902
http://dx.doi.org/10.1111/j.1582-4934.2010.01089.x
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