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Blood, 1 April 2005, Vol. 105, No. 7, pp. 2787-2792.
Prepublished online as a Blood First Edition Paper on December 14, 2004; DOI 10.1182/blood-2004-09-3388.


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IMMUNOBIOLOGY

Ly49Q defines 2 pDC subsets in mice

Yumiko Kamogawa-Schifter, Jun Ohkawa, Sahori Namiki, Naoko Arai, Ken-ichi Arai, and YongJun Liu

From the Department of Immunobiology, Ginkgo Biomedical Research Institute, Tokyo, Japan; Department of Molecular and Developmental Biology, Institute of Medical Science, University of Tokyo, Tokyo, Japan; Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan; and Department of Immunology, MD Anderson Cancer Center, University of Texas, Houston, TX.

Plasmacytoid dendritic cells (pDCs) play an important primary role for antiviral innate immunity by rapidly producing large amounts of type 1 interferon (IFN) upon viral infection. To study pDC biology, we generated a monoclonal antibody, termed 2E6, that recognizes pDCs. Molecular cloning of a cDNA encoding the 2E6 antigen revealed that it is a type II C-type lectin, Ly49Q, that consists of 247 amino acids with high homology to the natural killer (NK) receptor family Ly49, with an immunoreceptor tyrosine-based inhibitory motif in the cytoplasmic domain. Ly49Q is expressed on pDCs but not on NK cells or myeloid dendritic cells. B220+, CD11c+, CD11b pDCs in bone marrow were divided into Ly49Q+ and Ly49Q subsets. While both subsets produced IFN-{alpha} upon cytosine-phosphate-guanosine (CpG) and herpes simplex virus stimulation, Ly49Q pDCs responded poorly to influenza virus. In addition, Ly49Q pDCs produced inflammatory cytokines such as interleukin 6 (IL-6), IL-12, and tumor necrosis factor {alpha} (TNF-{alpha}) upon stimulation at lower levels than those produced by Ly49Q+ pDCs. In contrast to bone marrow, Ly49Q+ pDCs were only found in peripheral blood, lymph nodes, and spleen. These results indicate that Ly49Q is a specific marker for peripheral pDCs and that expression of Ly49Q defines 2 subsets of pDCs in bone marrow.


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