Macrophages and dendritic cells (DCs) are crucial for immune and inflammatory responses and belong to a network of cells that has been termed the mononuclear phagocyte system (MPS). However, the origin and lineage of these cells remain poorly understood. Here, we describe the isolation and clonal analysis of a mouse bone marrow progenitor that is specific for monocytes, several macrophage subsets, and resident spleen DCs in vivo. It was also possible to recapitulate this differentiation in vitro by using treatment with the cytokines macrophage colony-stimulating factor and granulocyte-macrophage colony-stimulating factor. Thus, macrophages and DCs appear to renew from a common progenitor, providing a cellular and molecular basis for the concept of the MPS.
Journal article
A clonogenic bone harrow progenitor specific for macrophages and dendritic cells
Science, Vol.311(5757), pp.83-87
06/Jan/2006
PMID: 16322423
Abstract
Details
- Title
- A clonogenic bone harrow progenitor specific for macrophages and dendritic cells
- Creators
- Darin K. Fogg (null) - Necker-Enfants Malades Hospital (France, Paris)Claire Sibon (null) - Necker-Enfants Malades Hospital (France, Paris)Chaouki Miled (null) - Necker-Enfants Malades Hospital (France, Paris)Steffen Jung (null) - 972WIS_INST___120Pierre Aucouturier (null) - InsermDan R. Littman (null) - NYU Langone HealthAna Cumano (null) - InsermFrederic Geissmann (Corresponding Author) - Necker-Enfants Malades Hospital (France, Paris)
- Resource Type
- Journal article
- Publication Details
- Science, Vol.311(5757), pp.83-87; 06/Jan/2006
- Number of pages
- 5
- Language
- English
- DOI
- https://doi.org/10.1126/science.1117729
- PMID
- 16322423
- Grant note
- The authors thank P. Leenen and B. Rocha for the kind gift of antibodies; J. Megret and C. Cordier for expert help with cell sorting; the members of the Geissmann lab for helpful discussions and critical analysis of the experiments and of the manuscript; and P. Kelly, N. Brousse, P. Berche, and J. L. Casanova for support. D.K.F. was supported by the INSERM (poste vert), C.S. was supported by the Fondation pour la Recherche Medicale (FRM) and the Fond d'Etude et de Recherche du Corps Médical des Hôpitaux de Paris, C.M. by the Fondation Schlumberger, and D.R.L. by NIH grant A133856. F.G. was supported by young investigator awards from INSERM (Avenir award), the City of Paris, the FRM, the Fondation de France, and the Fondation Schlumberger.
- Record Identifier
- 993267811203596
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