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Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers

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 hamper...

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Autores principales: Matsuda, Jennifer L., Naidenko, Olga V., Gapin, Laurent, Nakayama, Toshinori, Taniguchi, Masaru, Wang, Chyung-Ru, Koezuka, Yasuhiko, Kronenberg, Mitchell
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193268/
https://www.ncbi.nlm.nih.gov/pubmed/10974039
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author Matsuda, Jennifer L.
Naidenko, Olga V.
Gapin, Laurent
Nakayama, Toshinori
Taniguchi, Masaru
Wang, Chyung-Ru
Koezuka, Yasuhiko
Kronenberg, Mitchell
author_facet Matsuda, Jennifer L.
Naidenko, Olga V.
Gapin, Laurent
Nakayama, Toshinori
Taniguchi, Masaru
Wang, Chyung-Ru
Koezuka, Yasuhiko
Kronenberg, Mitchell
author_sort Matsuda, Jennifer L.
collection PubMed
description 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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spelling pubmed-21932682008-04-16 Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers Matsuda, Jennifer L. Naidenko, Olga V. Gapin, Laurent Nakayama, Toshinori Taniguchi, Masaru Wang, Chyung-Ru Koezuka, Yasuhiko Kronenberg, Mitchell J Exp Med Original Article 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. The Rockefeller University Press 2000-09-05 /pmc/articles/PMC2193268/ /pubmed/10974039 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Original Article
Matsuda, Jennifer L.
Naidenko, Olga V.
Gapin, Laurent
Nakayama, Toshinori
Taniguchi, Masaru
Wang, Chyung-Ru
Koezuka, Yasuhiko
Kronenberg, Mitchell
Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title_full Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title_fullStr Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title_full_unstemmed Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title_short Tracking the Response of Natural Killer T Cells to a Glycolipid Antigen Using Cd1d Tetramers
title_sort tracking the response of natural killer t cells to a glycolipid antigen using cd1d tetramers
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2193268/
https://www.ncbi.nlm.nih.gov/pubmed/10974039
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