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Prepublished online as a Blood First Edition Paper on May 24, 2002; DOI 10.1182/blood-2002-01-0214.

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2002-01-0214v1
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Submitted January 28, 2002
Accepted December 31, 1969

Mouse CD11c+ B220+ Gr1+ plasmacytoid dendritic cells develop independently of the T cell lineage

Isabel Ferrero, Werner Held, Anne Wilson, Fabienne Tacchini-Cottier, Freddy Radtke, and H R MacDonald*

Ludwig Institute for Cancer Research, Lausanne Branch, Lausanne Branch, University of Lausanne, Epalinges, Switzerland
WHO Immunology Research and Training Center, Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland

* Corresponding author; email: Hughrobson.Macdonald{at}isrec.unil.ch.

The developmental origin of dendritic cells (DC) is controversial. In the mouse CD8{alpha}+ and CD8{alpha}- DC subsets are often considered to be of lymphoid and myeloid origin respectively, although evidence on this point is conflicting. Very recently a novel CD11c+ B220+ DC subset has been identified that appears to be the murine counterpart to IFN{alpha}-producing human plasmacytoid DC (PDC). We show here that CD11c+ B220+ mouse PDC, like human PDC, are present in the thymus and express T lineage markers such as CD8{alpha} and CD4. However the intrathymic development of PDC can be completely dissociated from immature T lineage cells in mixed chimeras established with bone marrow cells from mice deficient for either Notch1 or T cell factor 1, two independent mutations that severely block early T cell development. Our data indicate that thymic PDC do not arise from a bipotential T/DC precursor.


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