The CD45RAhiCD11cint plasmacytoid predendritic cells (p-preDCs) of mouse lymphoid organs, when stimulated in culture with CpG or influenza virus, produce large amounts of type I interferons and transform without division into CD8+CD205− DCs. P-preDCs express CIRE, the murine equivalent of DC-specific intercellular adhesion molecule 3 grabbing nonintegrin (DC-SIGN). P-preDCs are divisible by CD4 expression into two subgroups differing in turnover rate and in response to Staphylococcus aureus. The kinetics of bromodeoxyuridine labeling and the results of transfer to normal recipient mice indicate that CD4− p-preDCs are the immediate precursors of CD4+ p-preDCs. Similar experiments indicate that p-preDCs are normally long lived and are not the precursors of the short-lived steady-state conventional DCs. However, in line with the culture studies on transfer to influenza virus-stimulated mice the p-preDCs transform into CD8+CD205− DCs, distinct from conventional CD8+CD205+ DCs. Hence as well as activating preexistant DCs, microbial infection induces a wave of production of a new DC subtype. The functional implications of this shift in the DC network remain to be determined.
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18 November 2002
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November 18 2002
Mouse Plasmacytoid Cells : Long-lived Cells, Heterogeneous in Surface Phenotype and Function, that Differentiate Into CD8+ Dendritic Cells Only after Microbial Stimulus
Meredith O'Keeffe,
Meredith O'Keeffe
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Hubertus Hochrein,
Hubertus Hochrein
2Institute of Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany
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David Vremec,
David Vremec
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Irina Caminschi,
Irina Caminschi
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Joanna L. Miller,
Joanna L. Miller
3Department of Microbiology and Immunology, The University of Melbourne, Victoria 3010, Australia
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E. Margot Anders,
E. Margot Anders
3Department of Microbiology and Immunology, The University of Melbourne, Victoria 3010, Australia
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Li Wu,
Li Wu
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Mireille H. Lahoud,
Mireille H. Lahoud
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Sandrine Henri,
Sandrine Henri
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Bernadette Scott,
Bernadette Scott
5Centre for Functional Genomics and Human Disease, Monash Institute of Reproduction and Development, Clayton, Victoria 3168, Australia
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Paul Hertzog,
Paul Hertzog
5Centre for Functional Genomics and Human Disease, Monash Institute of Reproduction and Development, Clayton, Victoria 3168, Australia
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Lilliana Tatarczuch,
Lilliana Tatarczuch
4Department of Veterinary Science, The University of Melbourne, Victoria 3010, Australia
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Ken Shortman
Ken Shortman
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
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Meredith O'Keeffe
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Hubertus Hochrein
2Institute of Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Munich, Germany
David Vremec
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Irina Caminschi
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Joanna L. Miller
3Department of Microbiology and Immunology, The University of Melbourne, Victoria 3010, Australia
E. Margot Anders
3Department of Microbiology and Immunology, The University of Melbourne, Victoria 3010, Australia
Li Wu
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Mireille H. Lahoud
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Sandrine Henri
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Bernadette Scott
5Centre for Functional Genomics and Human Disease, Monash Institute of Reproduction and Development, Clayton, Victoria 3168, Australia
Paul Hertzog
5Centre for Functional Genomics and Human Disease, Monash Institute of Reproduction and Development, Clayton, Victoria 3168, Australia
Lilliana Tatarczuch
4Department of Veterinary Science, The University of Melbourne, Victoria 3010, Australia
Ken Shortman
1The Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria 3050, Australia
Address correspondence to Dr. Meredith O'Keeffe, The Walter and Eliza Hall Institute of Medical Research, P.O. Royal Melbourne Hospital, Victoria 3050, Australia. Phone: 61-3-9345-2533; Fax: 61-3-9347-0852; E-mail: [email protected]
*
Abbreviations used in this paper: DC, dendritic cell; p-preDC, plasmacytoid preDC; PI, propidium iodide; SAC, Staphylococcus aureus.
Received:
June 21 2002
Accepted:
September 17 2002
Revision Received:
October 07 2002
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2002
J Exp Med (2002) 196 (10): 1307–1319.
Article history
Received:
June 21 2002
Accepted:
September 17 2002
Revision Received:
October 07 2002
Citation
Meredith O'Keeffe, Hubertus Hochrein, David Vremec, Irina Caminschi, Joanna L. Miller, E. Margot Anders, Li Wu, Mireille H. Lahoud, Sandrine Henri, Bernadette Scott, Paul Hertzog, Lilliana Tatarczuch, Ken Shortman; Mouse Plasmacytoid Cells : Long-lived Cells, Heterogeneous in Surface Phenotype and Function, that Differentiate Into CD8+ Dendritic Cells Only after Microbial Stimulus . J Exp Med 18 November 2002; 196 (10): 1307–1319. doi: https://doi.org/10.1084/jem.20021031
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