TY - JOUR
T1 - CD1d-expressing dendritic cells but not thymic epithelial cells can mediate negative selection of NKT cells
AU - Chun, Taehoon
AU - Page, Michael J.
AU - Gapin, Laurent
AU - Matsuda, Jennifer L.
AU - Xu, Honglin
AU - Nguyen, Hanh
AU - Kang, Hyung Sik
AU - Stanic, Aleksandar K.
AU - Joyce, Sebastian
AU - Koltun, Walter A.
AU - Chorney, Michael J.
AU - Kronenberg, Mitchell
AU - Wang, Chyung Ru
PY - 2003/4
Y1 - 2003/4
N2 - 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 α-galactosylceramide (α-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 Vβ 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.
AB - 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 α-galactosylceramide (α-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 Vβ 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.
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U2 - 10.1084/jem.20021366
DO - 10.1084/jem.20021366
M3 - Article
C2 - 12682110
AN - SCOPUS:0344837838
SN - 0022-1007
VL - 197
SP - 907
EP - 918
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 7
ER -