Glycolipid presentation to natural killer T cells differs in an organ-dependent fashion

被引:99
作者
Schmieg, J
Yang, GG
Franck, RW
Van Rooijen, N
Tsuji, M [1 ]
机构
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[2] CUNY Hunter Coll, Dept Chem, New York, NY 10021 USA
[3] Free Univ Amsterdam, Fac Med, Dept Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
[4] NYU, Sch Med, Dept Med & Mol Parasitol, New York, NY 10010 USA
关键词
dendritic cell; Kupffer cell;
D O I
10.1073/pnas.0408288102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
It has been shown that dendritic cells (DCs) are able to present glycolipids to natural killer (NK) T cells in vivo. However, the essential role of DCs, as well as the role of other cells in glycolipid presentation, is unknown. Here, we show that DCs are the crucial antigen-presenting cells (APCs) for splenic NK T cells, whereas Kupffer cells are the key APCs for hepatic NK T cells. Both cell types stimulate cytokine production by NK T cells within 2 h of glycolipid administration, but only DCs are involved in the systemic, downstream responses to glycolipid administration. More specifically, CD8alpha+ DCs produce IL-12 in response to glycolipid presentation, which stimulates secondary IFN-gamma production by NK cells in different organs. Different APCs participate in glycolipid presentation to NK T cells in vivo but differ in their involvement in the overall glycolipid response.
引用
收藏
页码:1127 / 1132
页数:6
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