Differential production of inflammatory chemokines by murine dendritic cell subsets.

Dendritic cells (DC) are efficient antigen presenting cells with the ability to activate naïve T cells. Murine DC represent a heterogeneous population that can be subdivided into distinct subsets, including the conventional DC (cDC) which are either CD4(-)CD8(-) (DN), CD4(+)CD8(-) (CD4+) or CD4(-)CD...

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Main Authors: Proietto, A, O'Keeffe, M, Gartlan, K, Wright, MD, Shortman, K, Wu, L, Lahoud, M
Format: Journal article
Language:English
Published: 2004
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author Proietto, A
O'Keeffe, M
Gartlan, K
Wright, MD
Shortman, K
Wu, L
Lahoud, M
author_facet Proietto, A
O'Keeffe, M
Gartlan, K
Wright, MD
Shortman, K
Wu, L
Lahoud, M
author_sort Proietto, A
collection OXFORD
description Dendritic cells (DC) are efficient antigen presenting cells with the ability to activate naïve T cells. Murine DC represent a heterogeneous population that can be subdivided into distinct subsets, including the conventional DC (cDC) which are either CD4(-)CD8(-) (DN), CD4(+)CD8(-) (CD4+) or CD4(-)CD8(+) (CD8+) subsets and the plasmacytoid DC (pDC), which have different immune regulatory functions. In this study, we investigated the differential expression of genes encoding the inflammatory chemokines Mip-1alpha, Mip-1beta and Rantes, and the secretion of these chemokines, among splenic DC subsets. These chemokine genes were expressed at higher levels by the splenic CD4+ and DN cDC subsets compared with the CD8+ cDC, in both the resting and activated states in vivo. Both the pDC and cDC subsets displayed increases in chemokine secretion in response to a range of toll-like receptor (TLR) stimuli in vitro. Whilst the pDC were the highest producers of Mip-1alpha and Mip-1beta in response to some TLR stimuli, the DN and CD4+ cDC subsets were the superior producers of Rantes. Overall, of the cDC, the CD4+ cDC produced all chemokines most efficiently, both at a basal level, and in response to most TLR stimuli. Thus, we report a new functional difference between the murine splenic cDC subsets, with the CD4+ cDC demonstrating the most efficient production of the inflammatory chemokines Mip-1alpha, Mip-1beta and Rantes.
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spelling oxford-uuid:f5c01b4b-d915-4b82-8407-b615b17b4d9e2022-03-27T12:29:38ZDifferential production of inflammatory chemokines by murine dendritic cell subsets.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:f5c01b4b-d915-4b82-8407-b615b17b4d9eEnglishSymplectic Elements at Oxford2004Proietto, AO'Keeffe, MGartlan, KWright, MDShortman, KWu, LLahoud, MDendritic cells (DC) are efficient antigen presenting cells with the ability to activate naïve T cells. Murine DC represent a heterogeneous population that can be subdivided into distinct subsets, including the conventional DC (cDC) which are either CD4(-)CD8(-) (DN), CD4(+)CD8(-) (CD4+) or CD4(-)CD8(+) (CD8+) subsets and the plasmacytoid DC (pDC), which have different immune regulatory functions. In this study, we investigated the differential expression of genes encoding the inflammatory chemokines Mip-1alpha, Mip-1beta and Rantes, and the secretion of these chemokines, among splenic DC subsets. These chemokine genes were expressed at higher levels by the splenic CD4+ and DN cDC subsets compared with the CD8+ cDC, in both the resting and activated states in vivo. Both the pDC and cDC subsets displayed increases in chemokine secretion in response to a range of toll-like receptor (TLR) stimuli in vitro. Whilst the pDC were the highest producers of Mip-1alpha and Mip-1beta in response to some TLR stimuli, the DN and CD4+ cDC subsets were the superior producers of Rantes. Overall, of the cDC, the CD4+ cDC produced all chemokines most efficiently, both at a basal level, and in response to most TLR stimuli. Thus, we report a new functional difference between the murine splenic cDC subsets, with the CD4+ cDC demonstrating the most efficient production of the inflammatory chemokines Mip-1alpha, Mip-1beta and Rantes.
spellingShingle Proietto, A
O'Keeffe, M
Gartlan, K
Wright, MD
Shortman, K
Wu, L
Lahoud, M
Differential production of inflammatory chemokines by murine dendritic cell subsets.
title Differential production of inflammatory chemokines by murine dendritic cell subsets.
title_full Differential production of inflammatory chemokines by murine dendritic cell subsets.
title_fullStr Differential production of inflammatory chemokines by murine dendritic cell subsets.
title_full_unstemmed Differential production of inflammatory chemokines by murine dendritic cell subsets.
title_short Differential production of inflammatory chemokines by murine dendritic cell subsets.
title_sort differential production of inflammatory chemokines by murine dendritic cell subsets
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