Function of NKG2D in natural killer cell-mediated rejection of mouse bone marrow grafts

被引:134
作者
Ogasawara, K
Benjamin, J
Takaki, R
Phillips, JH
Lanier, LL [1 ]
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
[3] Int Med Ctr Japan, Res Inst, Div Clin Immunol, Dept Intractable Dis,Shinjuku Ku, Tokyo 1628655, Japan
[4] Univ Calif San Francisco, Biomed Sci Grad Program, San Francisco, CA 94143 USA
[5] Schering Plough BioPharma, Palo Alto, CA 94304 USA
关键词
D O I
10.1038/ni1236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Irradiation- resistant natural killer ( NK) cells in an F-1 recipient can reject parental bone marrow, and host NK cells can also prevent engraftment of allogeneic bone marrow. We show here that repopulating bone marrow cells in certain mouse strains expressed retinoic acid early inducible 1 proteins, which are ligands for the activating NKG2D NK cell receptor. Treatment with a neutralizing antibody to NKG2D prevented rejection of parental BALB/ c bone marrow in ( C57BL/ 6 x BALB/ c) F1 recipients and allowed engraftment of allogeneic BALB. B bone marrow in C57BL/ 6 recipients. Additionally, bone marrow from C57BL/ 6 mice transgenic for retinoic acid early inducible 1 epsilon was rejected by syngeneic mice but was accepted after treatment with antibody to NKG2D. If other stem cells or tissues upregulate expression of NKG2D ligands after transplantation, NKG2D may contribute to graft rejection in immunocompetent hosts.
引用
收藏
页码:938 / 945
页数:8
相关论文
共 40 条
[1]   Hematopoietic stem cells are not direct cytotoxic targets of natural killer cells [J].
Aguila, HL ;
Weissman, IL .
BLOOD, 1996, 87 (04) :1225-1231
[2]   DAP12-deficient mice fail to develop autoimmunity due to impaired antigen priming [J].
Bakker, ABH ;
Hoek, RM ;
Cerwenka, A ;
Blom, B ;
Lucian, L ;
McNeil, T ;
Murray, R ;
Phillips, JH ;
Sedgwick, JD ;
Lanier, LL .
IMMUNITY, 2000, 13 (03) :345-353
[3]   REJECTION OF CLASS-I MHC-DEFICIENT HEMATOPOIETIC-CELLS BY IRRADIATED MHC-MATCHED MICE [J].
BIX, M ;
LIAO, NS ;
ZIJLSTRA, M ;
LORING, J ;
JAENISCH, R ;
RAULET, D .
NATURE, 1991, 349 (6307) :329-331
[4]   Cutting edge: Murine UL16-binding protein-like transcript 1: A newly described transcript encoding a high-affinity ligand for marine NKG2D [J].
Carayannopoulos, LN ;
Naidenko, OV ;
Fremont, DH ;
Yokoyama, WM .
JOURNAL OF IMMUNOLOGY, 2002, 169 (08) :4079-4083
[5]   Retinoic acid early inducible genes define a ligand family for the activating NKG2D receptor in mice [J].
Cerwenka, A ;
Bakker, ABH ;
McClanahan, T ;
Wagner, J ;
Wu, J ;
Phillips, JH ;
Lanier, LL .
IMMUNITY, 2000, 12 (06) :721-727
[6]   NKG2D ligands: unconventional MHC class I-like molecules exploited by viruses and cancer [J].
Cerwenka, A ;
Lanier, LL .
TISSUE ANTIGENS, 2003, 61 (05) :335-343
[7]   INDUCTION OF IMMUNITY + OF UNRESPONSIVENESS TO PARENTAL MARROW GRAFTS IN ADULT F1 HYBRID MICE [J].
CUDKOWICZ, G ;
STIMPFLING, JH .
NATURE, 1964, 204 (495) :450-&
[8]   PECULIAR IMMUNOBIOLOGY OF BONE MARROW ALLOGRAFTS .2. REJECTION OF PARENTAL GRAFTS BY RESISTANT F1 HYBRID MICE [J].
CUDKOWICZ, G ;
BENNETT, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1971, 134 (06) :1513-+
[9]   Ligands for the murine NKG2D receptor: expression by tumor cells and activation of NK cells and macrophages [J].
Diefenbach, A ;
Jamieson, AM ;
Liu, SD ;
Shastri, N ;
Raulet, DH .
NATURE IMMUNOLOGY, 2000, 1 (02) :119-126
[10]   Selective associations with signaling proteins determine stimulatory versus costimulatory activity of NKG2D [J].
Diefenbach, A ;
Tomasello, E ;
Lucas, M ;
Jamieson, AM ;
Hsia, JK ;
Vivier, E ;
Raulet, DH .
NATURE IMMUNOLOGY, 2002, 3 (12) :1142-1149