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* Immunology Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia; and
INSERM Unité 932, Institut Curie, Paris, France
Mouse lymphoid organs contain two major subsets of dendritic cells (DC) that differ in their phenotype and functions: conventional DC (cDC) and plasmacytoid DC (pDC). Recently, it has been proposed that differential expression of CCR9 could distinguish functionally distinct pDC subsets. We show that B220+CCR9– DC do not express classical pDC markers and have a developmental origin different from that of pDC. Furthermore, B220+CCR9– DC do not secrete IFN-
in response to CpG and, unlike pDC, can efficiently present exogenous Ags. Our results demonstrate that B220+CCR9– DC do not represent a subset of pDC. After in vivo transfer, these cells down-regulate B220 expression and convert into the two major cDC subsets, showing that they are a developmental stage of cDC differentiation.
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1 This work was supported by the National Health and Medical Research Council of Australia (to J.A.V.), the Leukemia and Lymphoma Society (to J.A.V.), and Marie Curie Fellowships from the European Commission (to E.S.).
2 Address correspondence and reprint requests to Dr. José A. Villadangos and Dr. Elodie Segura, Immunology Division, Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, Victoria 3050, Australia. E-mail addresses: villadangos{at}wehi.edu.au and segura{at}wehi.edu.au
3 Abbreviations used in this paper: DC, dendritic cell; cDC, conventional DC; Ftl3L, Fms-like tyrosine kinase 3 ligand; int, intermediate; pDC, plasmacytoid DC; Flt3L.
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