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Characterization of the effect of LPS on dendritic cell subset discrimination in spleen

The Gram-negative bacterial endotoxin lipopolysaccharide (LPS) is a potent inflammatory mediator and a leading cause of bacterial sepsis. While LPS is known to activate antigen-presenting cells, here we find that LPS down-regulates expression of CD11c and CD11b on splenic dendritic cell subsets, thu...

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Detalles Bibliográficos
Autores principales: Griffiths, Kristin L, Tan, Jonathan KH, O'Neill, Helen C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196665/
https://www.ncbi.nlm.nih.gov/pubmed/24913604
http://dx.doi.org/10.1111/jcmm.12332
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author Griffiths, Kristin L
Tan, Jonathan KH
O'Neill, Helen C
author_facet Griffiths, Kristin L
Tan, Jonathan KH
O'Neill, Helen C
author_sort Griffiths, Kristin L
collection PubMed
description The Gram-negative bacterial endotoxin lipopolysaccharide (LPS) is a potent inflammatory mediator and a leading cause of bacterial sepsis. While LPS is known to activate antigen-presenting cells, here we find that LPS down-regulates expression of CD11c and CD11b on splenic dendritic cell subsets, thus confounding the ability to identify these subsets following treatment. This has implications with regard to tracking the response to LPS in terms of the cell subsets involved, and should be considered whenever such studies are undertaken.
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spelling pubmed-41966652014-12-03 Characterization of the effect of LPS on dendritic cell subset discrimination in spleen Griffiths, Kristin L Tan, Jonathan KH O'Neill, Helen C J Cell Mol Med Short Communication The Gram-negative bacterial endotoxin lipopolysaccharide (LPS) is a potent inflammatory mediator and a leading cause of bacterial sepsis. While LPS is known to activate antigen-presenting cells, here we find that LPS down-regulates expression of CD11c and CD11b on splenic dendritic cell subsets, thus confounding the ability to identify these subsets following treatment. This has implications with regard to tracking the response to LPS in terms of the cell subsets involved, and should be considered whenever such studies are undertaken. Blackwell Publishing Ltd 2014-09 2014-06-10 /pmc/articles/PMC4196665/ /pubmed/24913604 http://dx.doi.org/10.1111/jcmm.12332 Text en © 2014 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Griffiths, Kristin L
Tan, Jonathan KH
O'Neill, Helen C
Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title_full Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title_fullStr Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title_full_unstemmed Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title_short Characterization of the effect of LPS on dendritic cell subset discrimination in spleen
title_sort characterization of the effect of lps on dendritic cell subset discrimination in spleen
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4196665/
https://www.ncbi.nlm.nih.gov/pubmed/24913604
http://dx.doi.org/10.1111/jcmm.12332
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