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

被引:38
作者
Ferrero, I
Held, W
Wilson, A
Tacchini-Cottier, F
Radtke, F
MacDonald, HR [1 ]
机构
[1] Univ Lausanne, Ludwig Inst Canc Res, Lausanne Branch, CH-1066 Epalinges, Switzerland
[2] Univ Lausanne, WHO, Immunol Res & Training Ctr, Inst Biochem, CH-1066 Epalinges, Switzerland
关键词
D O I
10.1182/blood-2002-01-0214
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The developmental origin of dendritic cells (DCs) is controversial. In the mouse CD8alpha(+) and CD8alpha(-) 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 interferon alpha (IFNalpha)-producing human plasmacytoid DCs (PDCs). We show here that CD11c(+) B220(+) mouse PDCs, like human PDCs, are present in the thymus and express T lineage markers such as CD8alpha and CD4. However, the intrathymic development of PDCs can be completely dissociated from immature T lineage cells in mixed chimeras established with bone marrow cells from mice deficient for either Notch-1 or T-cell factor 1, two independent mutations that severely block early T-cell development. Our data indicate that thymic PDCs do not arise from a bipotential T/DC precursor.
引用
收藏
页码:2852 / 2857
页数:6
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