Down-regulation of the invariant Vα14 antigen receptor in NKT cells upon activation

被引:123
作者
Harada, M
Seino, K
Wakao, H
Sakata, S
Ishizuka, Y
Ito, T
Kojo, S
Nakayama, T
Taniguchi, M
机构
[1] Chiba Univ, Grad Sch Med, Dept Mol Immunol, RIKEN Res Ctr Allergy & Immunol,Chuo Ku, Chiba 2608670, Japan
[2] JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
[3] Chiba Univ, Grad Sch Med, Dept Med Immunol, Chiba 2608670, Japan
关键词
alpha-galactosylceramide; apoptosis; CD1d tetramer; cDNA array; cytokine production;
D O I
10.1093/intimm/dxh023
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NKT cells expressing the invariant Valpha14 antigen receptor constitute a novel lymphocyte subpopulation with immunoregulatory functions. Stimulation via their invariant Valpha14 receptor with anti-CD3 or a ligand, alpha-galactosylceramide (alpha-GalCer), triggers activation of Valpha14 NKT cells, resulting in a rapid cytokine production such as IFN-gamma and IL-4. Soon after their receptor activation, Valpha14 NKT cells disappeared as judged by staining with CD1d tetramer loaded with alpha-GalCer (alpha-GalCer/CD1d tetramer), which has been believed to be due to apoptotic cell death. Here we show that such a disappearance was largely attributed to down-regulation of the Valpha14 receptor. In fact, Valpha14 NKT cells were relatively resistant to apoptosis compared to the conventional T cells as evidenced by less staining with Annexin-V, a limited DNA fragmentation, and their preferential expression of anti-apoptotic genes such as NAIP and MyD118. Furthermore, they did not become tolerant, and maintained their proliferative capacity and cytokine production even after their receptor down-regulation. These as yet unrecognized facets of Valpha14 NKT cells are discussed in relation to their regulatory functions.
引用
收藏
页码:241 / 247
页数:7
相关论文
共 23 条
[1]   Modulation of Fas-dependent apoptosis: A dynamic process controlling both the persistence and death of CD4 regulatory T cells and effector T cells [J].
Banz, A ;
Pontoux, C ;
Papiernik, M .
JOURNAL OF IMMUNOLOGY, 2002, 169 (02) :750-757
[2]   CD1 RECOGNITION BY MOUSE NK1(+) T-LYMPHOCYTES [J].
BENDELAC, A ;
LANTZ, O ;
QUIMBY, ME ;
YEWDELL, JW ;
BENNINK, JR ;
BRUTKIEWICZ, RR .
SCIENCE, 1995, 268 (5212) :863-865
[3]  
Chen YR, 2000, INT J ONCOL, V16, P651
[4]   Requirement for V(alpha)14 NKT cells in IL-12-mediated rejection of tumors [J].
Cui, JQ ;
Shin, T ;
Kawano, T ;
Sato, H ;
Kondo, E ;
Toura, I ;
Kaneko, Y ;
Koseki, H ;
Kanno, M ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1623-1626
[5]   Induction of gadd45β by NF-κB downregulates pro-apoptotic JNK signalling [J].
De Smaele, E ;
Zazzeroni, F ;
Papa, S ;
Nguyen, DU ;
Jin, RG ;
Jones, J ;
Cong, R ;
Franzoso, G .
NATURE, 2001, 414 (6861) :308-313
[6]   Rapid death and regeneration of NKT cells in anti-CD3ε- or IL-12-treated mice:: A major role for bone marrow in NKT cell homeostasis [J].
Eberl, G ;
MacDonald, HR .
IMMUNITY, 1998, 9 (03) :345-353
[7]   Prolonged IFN-γ-producing NKT response induced with α-galactosylceramide-loaded DCs [J].
Fujii, S ;
Shimizu, K ;
Kronenberg, M ;
Steinman, RM .
NATURE IMMUNOLOGY, 2002, 3 (09) :867-+
[8]   The neuronal apoptosis inhibitory protein suppresses neuronal differentiation and apoptosis in PC12 cells [J].
Götz, R ;
Karch, C ;
Digby, MR ;
Troppmair, J ;
Rapp, UR ;
Sendtner, M .
HUMAN MOLECULAR GENETICS, 2000, 9 (17) :2479-2489
[9]   Augmentation of Vα14 NKT cell-mediated cytotoxicity by interleukin 4 in an autocrine mechanism resulting in the development of concanavalin A-induced hepatitis [J].
Kaneko, Y ;
Harada, M ;
Kawano, T ;
Yamashita, M ;
Shibata, Y ;
Gejyo, F ;
Nakayama, T ;
Taniguchi, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (01) :105-114
[10]   CD1d-restricted and TCR-mediated activation of V(alpha)14 NKT cells by glycosylceramides [J].
Kawano, T ;
Cui, JQ ;
Koezuka, Y ;
Toura, I ;
Kaneko, Y ;
Motoki, K ;
Ueno, H ;
Nakagawa, R ;
Sato, H ;
Kondo, E ;
Koseki, H ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1626-1629