Interferon-producing killer dendritic cells (IKDCs) are a recently described subset of CD11cloB220+ cells that share phenotypic and functional properties of DCs and natural killer (NK) cells (Chan, C.W., E. Crafton, H.N. Fan, J. Flook, K. Yoshimura, M. Skarica, D. Brockstedt, T.W. Dubensky, M.F. Stins, L.L. Lanier, et al. 2006. Nat. Med. 12:207–213; Taieb, J., N. Chaput, C. Menard, L. Apetoh, E. Ullrich, M. Bonmort, M. Pequignot, N. Casares, M. Terme, C. Flament, et al. 2006. Nat. Med. 12:214–219). IKDC development appears unusual in that cytokines using the interleukin (IL)-2 receptor β (IL-2Rβ) chain but not those using the common γ chain (γc) are necessary for their generation. By directly comparing Rag2−/−γc−/y, Rag2−/−IL-2Rβ−/−, Rag2−/−IL-15−/−, and Rag2−/−IL-2−/− mice, we demonstrate that IKDC development parallels NK cell development in its strict IL-15 dependence. Moreover, IKDCs uniformly express NK-specific Ncr-1 transcripts (encoding NKp46), whereas NKp46+ cells are absent in Ncr1gfp/+γc−/y mice. Distinguishing features of IKDCs (CD11cloB220+MHC-II+) were carefully examined on developing NK cells in the bone marrow and on peripheral NK cells. As B220 expression was heterogeneous, defining B220lo versus B220hi NK1.1+ NK cells could be considered as arbitrary, and few phenotypic differences were noted between NK1.1+ NK cells bearing different levels of B220. CD11c expression did not correlate with B220 or major histocompatibility complex (MHC) class II (MHC-II) expression, and most MHC-II+ NK1.1+ cells did not express B220 and were thus not IKDCs. Finally, CD11c, MHC-II, and B220 levels were up-regulated on NK1.1+ cells upon activation in vitro or in vivo in a proliferation-dependent fashion. Our data suggest that the majority of CD11cloB220+ “IKDC-like” cells represent activated NK cells.
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29 October 2007
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October 08 2007
CD11cloB220+ interferon-producing killer dendritic cells are activated natural killer cells
Christian A.J. Vosshenrich,
Christian A.J. Vosshenrich
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Sarah Lesjean-Pottier,
Sarah Lesjean-Pottier
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Milena Hasan,
Milena Hasan
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Odile Richard-Le Goff,
Odile Richard-Le Goff
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Erwan Corcuff,
Erwan Corcuff
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Ofer Mandelboim,
Ofer Mandelboim
3The Lautenberg Center for General and Tumor Immunology, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel
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James P. Di Santo
James P. Di Santo
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
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Christian A.J. Vosshenrich
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
Sarah Lesjean-Pottier
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
Milena Hasan
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
Odile Richard-Le Goff
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
Erwan Corcuff
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
Ofer Mandelboim
3The Lautenberg Center for General and Tumor Immunology, The Hebrew University-Hadassah Medical School, Jerusalem 91120, Israel
James P. Di Santo
1Unité des Cytokines et Développement Lymphoide, Institut Pasteur, 75015 Paris, France
2Institut National de la Santé et de la Recherche Médicale U668, 75015 Paris, France
CORRESPONDENCE James P. Di Santo: [email protected]
Received:
July 13 2007
Accepted:
September 24 2007
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2007
J Exp Med (2007) 204 (11): 2569–2578.
Article history
Received:
July 13 2007
Accepted:
September 24 2007
Citation
Christian A.J. Vosshenrich, Sarah Lesjean-Pottier, Milena Hasan, Odile Richard-Le Goff, Erwan Corcuff, Ofer Mandelboim, James P. Di Santo; CD11cloB220+ interferon-producing killer dendritic cells are activated natural killer cells . J Exp Med 29 October 2007; 204 (11): 2569–2578. doi: https://doi.org/10.1084/jem.20071451
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