CD1d-expressing dendritic cells but not thymic epithelial cells can mediate negative selection of NKT cells

被引:118
作者
Chun, T
Page, MJ
Gapin, L
Matsuda, JL
Xu, HL
Nguyen, H
Kang, HS
Stanic, AK
Joyce, S
Koltun, WA
Chorney, MJ
Kronenberg, M
Wang, CR
机构
[1] Univ Chicago, Gwen Knapp Ctr Lupus & Immunol Res, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[4] Penn State Univ, Coll Med, Dept Surg, Hershey, PA 17033 USA
[5] La Jolla Inst Allergy & Immunol, San Diego, CA 92121 USA
[6] Vanderbilt Univ, Dept Microbiol & Immunol, Sch Med, Nashville, TN 37232 USA
关键词
NKT cells; CD1; negative selection; avidity model; lipid antigen;
D O I
10.1084/jem.20021366
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer T (NKT) cells are a unique immunoregulatory T cell population that is positively selected by CD1d-expressing thymocytes. Previous studies have shown that NKT cells exhibit autoreactivity, which raises the question of whether they are subject to negative selection. Here, we report that the addition of agonist glycolipid alpha-galactosylceramide (alpha-GalCer) to a fetal thymic organ culture (FTOC) induces a dose-dependent disappearance of NKT cells, suggesting that NKT cells are susceptible to negative selection. Overexpression of CD1d in transgenic (Tg) mice results in reduced numbers of NKT cells, and the residual NKT cells in CD1d-Tg mice exhibit both an altered Vbeta usage and a reduced sensitivity to antigen. Furthermore, bone marrow (BM) chimeras between Tg and WT mice reveal that CD1d-expressing BM-derived dendritic cells, but not thymic epithelial cells, mediate the efficient negative selection of NKT cells. Thus, our data suggest that NKT cells developmentally undergo negative selection when engaged by high-avidity antigen or abundant self-antigen.
引用
收藏
页码:907 / 918
页数:12
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