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Differential production of inflammatory chemokines by murine dendritic cell subsets.

Abstract:
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.
Publication status:
Published

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Publisher copy:
10.1016/j.imbio.2004.03.002

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
Pathology Dunn School
Role:
Author


Journal:
Immunobiology More from this journal
Volume:
209
Issue:
1-2
Pages:
163-172
Publication date:
2004-01-01
DOI:
EISSN:
1878-3279
ISSN:
0171-2985


Language:
English
Keywords:
Pubs id:
pubs:55296
UUID:
uuid:f5c01b4b-d915-4b82-8407-b615b17b4d9e
Local pid:
pubs:55296
Source identifiers:
55296
Deposit date:
2012-12-19
ARK identifier:

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