A major group of natural killer (NK) T cells express an invariant Vα14+ T cell receptor (TCR) specific for the lipoglycan α-galactosylceramide (α-GalCer), which is presented by CD1d. These cells may have an important immune regulatory function, but an understanding of their biology has been hampered by the lack of suitable reagents for tracking them in vivo. Here we show that tetramers of mouse CD1d loaded with α-GalCer are a sensitive and highly specific reagent for identifying Vα14+ NK T cells. Using these tetramers, we find that α-GalCer–specific T lymphocytes are more widely distributed than was previously appreciated, with populations of largely NK1.1− but tetramer-binding T cells present in the lymph nodes and the intestine. Injection of α-GalCer leads to the production of both interferon γ and interleukin 4 by nearly all NK T cells in the liver and the majority of the spleen within 2 h. These cells mostly disappear by 5 h, and they do not reappear after 1 wk. Curiously, tetramer-positive thymocytes do not rapidly synthesize cytokines, nor do they undergo decreases in cell number after lipid antigen stimulation, although they express equivalent TCR levels. In summary, the data presented here demonstrate that α-GalCer–specific NK T cells undergo a unique and highly compartmentalized response to antigenic stimulation.
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5 September 2000
Article|
September 05 2000
Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
Jennifer L. Matsuda,
Jennifer L. Matsuda
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
bDepartment of Biology, University of California at San Diego, San Diego, California 92093
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Olga V. Naidenko,
Olga V. Naidenko
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
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Laurent Gapin,
Laurent Gapin
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
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Toshinori Nakayama,
Toshinori Nakayama
cCREST (Core Research for Evolutional Science and Technology) and the Department of Molecular Immunology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan
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Masaru Taniguchi,
Masaru Taniguchi
cCREST (Core Research for Evolutional Science and Technology) and the Department of Molecular Immunology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan
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Chyung-Ru Wang,
Chyung-Ru Wang
dDepartment of Pathology, Gwenn Knapp Center For Lupus and Immunology Research, University of Chicago, Chicago, Illinois 60637
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Yasuhiko Koezuka,
Yasuhiko Koezuka
ePharmaceutical Research Laboratory, Kirin Brewery Company Limited, Gunma 370-12, Japan
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Mitchell Kronenberg
Mitchell Kronenberg
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
bDepartment of Biology, University of California at San Diego, San Diego, California 92093
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Jennifer L. Matsuda
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
bDepartment of Biology, University of California at San Diego, San Diego, California 92093
Olga V. Naidenko
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
Laurent Gapin
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
Toshinori Nakayama
cCREST (Core Research for Evolutional Science and Technology) and the Department of Molecular Immunology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan
Masaru Taniguchi
cCREST (Core Research for Evolutional Science and Technology) and the Department of Molecular Immunology, Chiba University Graduate School of Medicine, Chiba 260-8670, Japan
Chyung-Ru Wang
dDepartment of Pathology, Gwenn Knapp Center For Lupus and Immunology Research, University of Chicago, Chicago, Illinois 60637
Yasuhiko Koezuka
ePharmaceutical Research Laboratory, Kirin Brewery Company Limited, Gunma 370-12, Japan
Mitchell Kronenberg
aLa Jolla Institute for Allergy and Immunology, San Diego, California 92121
bDepartment of Biology, University of California at San Diego, San Diego, California 92093
Abbreviations used in this paper: DN, double-negative; α-GalCer, α-galactosylceramide; IELs, intestinal intraepithelial lymphocytes; LAK, lymphokine-activated killer.
J.L. Matsuda and O.V. Naidenko contributed equally to this work.
Received:
May 04 2000
Revision Requested:
June 14 2000
Accepted:
June 28 2000
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2000 The Rockefeller University Press
2000
The Rockefeller University Press
J Exp Med (2000) 192 (5): 741–754.
Article history
Received:
May 04 2000
Revision Requested:
June 14 2000
Accepted:
June 28 2000
Citation
Jennifer L. Matsuda, Olga V. Naidenko, Laurent Gapin, Toshinori Nakayama, Masaru Taniguchi, Chyung-Ru Wang, Yasuhiko Koezuka, Mitchell Kronenberg; Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers. J Exp Med 5 September 2000; 192 (5): 741–754. doi: https://doi.org/10.1084/jem.192.5.741
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