In Vivo Analysis of Dendritic Cell Development and Homeostasis

Kang Liu(Howard Hughes Medical Institute), Gabriel D. Victora(Howard Hughes Medical Institute), Tanja A. Schwickert(Howard Hughes Medical Institute), Pierre Guermonprez(Howard Hughes Medical Institute), Matthew M. Meredith(Howard Hughes Medical Institute), Kai-Hui Yao(Howard Hughes Medical Institute), Fei-Fan Chu(Howard Hughes Medical Institute), Gwendalyn J. Randolph(Howard Hughes Medical Institute), Alexander Y. Rudensky(Howard Hughes Medical Institute), Michel C. Nussenzweig(Howard Hughes Medical Institute)
Science
March 13, 2009
Cited by 915Open Access
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Abstract

Dendritic cells (DCs) in lymphoid tissue arise from precursors that also produce monocytes and plasmacytoid DCs (pDCs). Where DC and monocyte lineage commitment occurs and the nature of the DC precursor that migrates from the bone marrow to peripheral lymphoid organs are unknown. We show that DC development progresses from the macrophage and DC precursor to common DC precursors that give rise to pDCs and classical spleen DCs (cDCs), but not monocytes, and finally to committed precursors of cDCs (pre-cDCs). Pre-cDCs enter lymph nodes through and migrate along high endothelial venules and later disperse and integrate into the DC network. Further cDC development involves cell division, which is controlled in part by regulatory T cells and fms-like tyrosine kinase receptor-3.


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