In Vivo Analysis of Dendritic Cell Development and Homeostasis

Author:

Liu Kang1234,Victora Gabriel D.1234,Schwickert Tanja A.1234,Guermonprez Pierre1234,Meredith Matthew M.1234,Yao Kaihui1234,Chu Fei-Fan1234,Randolph Gwendalyn J.1234,Rudensky Alexander Y.1234,Nussenzweig Michel1234

Affiliation:

1. Laboratory of Molecular Immunology, Rockefeller University, New York, NY 10065, USA.

2. Department of Gene and Cell Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA.

3. Department of Immunology and Howard Hughes Medical Institute (HHMI), University of Washington, Seattle, WA 98195, USA.

4. HHMI, Rockefeller University, New York, NY 10021, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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