Journal article
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
- 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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- Copyright date:
- 2004
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