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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
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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. |
format | Online Article Text |
id | pubmed-3822631 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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