Consequence of the SLAM-SAP signaling pathway in innate-like and conventional lymphocytes

被引:98
作者
Veillette, Andre [1 ]
Dong, Zhongjun
Latour, Sylvain
机构
[1] Clin Res Inst Montreal, Mol Oncol Lab, Montreal, PQ H2W 1R7, Canada
[2] Univ Montreal, Dept Med, Montreal, PQ H2W 1R7, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H2W 1R7, Canada
关键词
D O I
10.1016/j.immuni.2007.11.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Signaling lymphocytic activation molecule (SLAM) family receptors mediate important regulatory signals in immune cells, as a result of their exquisite ability to associate with members of the SLAM-associated protein (SAP) family of adaptors. As discussed herein, recent findings show that the SLAM and SAP families carry out pivotal functions in innate-like and conventional lymphocytes. They are critically needed for the development of innate-like lymphocytes such as NKT cells. In addition, they influence several of the functions of conventional lymphocytes, including the ability of CD4(+) T cells to secrete certain cytokines and mediate B cell help; CD8(+) T cell proliferation and cytokine production; NK cell-mediated cytotoxicity; and B cell antibody production. These unique functional properties appear to be facilitated by the ability of SLAM-related receptors to serve as self-ligands during homotypic interactions between immune cells. The importance of the SLAM-SAP pathway in normal immunity is highlighted by the finding that SAP is mutated in humans suffering from the immunodeficiency X-linked lymphoproliferative disease.
引用
收藏
页码:698 / 710
页数:13
相关论文
共 96 条
[71]   X-linked lymphoproliferative disease: 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells [J].
Parolini, S ;
Bottino, C ;
Falco, M ;
Augugliaro, R ;
Giliani, S ;
Franceschini, R ;
Ochs, HD ;
Wolf, H ;
Bonnefoy, JY ;
Biassoni, R ;
Moretta, L ;
Notarangelo, LD ;
Moretta, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (03) :337-346
[72]   Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product [J].
Pasquier, B ;
Yin, L ;
Fondanèche, MC ;
Relouzat, F ;
Bloch-Queyrat, C ;
Lambert, N ;
Fischer, A ;
de Saint-Basile, G ;
Latour, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (05) :695-701
[73]   XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome [J].
Rigaud, Stephaine ;
Fondaneche, Marie-Claude ;
Lambert, Nathalie ;
Pasquier, Benoit ;
Mateo, Veronique ;
Soulas, Pauline ;
Galicier, Lionel ;
Le Deist, Francoise ;
Rieux-Laucat, Frederic ;
Revy, Patrick ;
Fischer, Alain ;
de Saint Basile, Genevieve ;
Latour, Sylvain .
NATURE, 2006, 444 (7115) :110-114
[74]   MHC class IB molecules bridge innate and acquired immunity [J].
Rodgers, JR ;
Cook, RG .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (06) :459-471
[75]   CD229 (Ly9) lymphocyte cell surface receptor interacts homophilically through its N-terminal domain and relocalizes to the immunological synapse [J].
Romero, X ;
Zapater, N ;
Calvo, M ;
Kalko, SG ;
de la Fuente, MA ;
Tovar, V ;
Ockeloen, C ;
Pizcueta, P ;
Engel, P .
JOURNAL OF IMMUNOLOGY, 2005, 174 (11) :7033-7042
[76]   Negative regulation of natural killer cell function by EAT-2, a SAP-related adaptor [J].
Roncagalli, R ;
Taylor, JER ;
Zhang, SH ;
Shi, XC ;
Chen, RY ;
Cruz-Munoz, ME ;
Yin, L ;
Latour, S ;
Veillette, A .
NATURE IMMUNOLOGY, 2005, 6 (10) :1002-1010
[77]   The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM [J].
Sayos, J ;
Wu, C ;
Morra, M ;
Wang, N ;
Zhang, X ;
Allen, D ;
van Schaik, S ;
Notarangelo, L ;
Geha, R ;
Roncarolo, MG ;
Oettgen, H ;
De Vries, JE ;
Aversa, G ;
Terhorst, C .
NATURE, 1998, 395 (6701) :462-469
[78]   Genome-wide screen for systemic lupus erythematosus susceptibility genes in multiplex families [J].
Shai, R ;
Quismorio, FP ;
Li, LL ;
Kwon, OJ ;
Morrison, J ;
Wallace, DJ ;
Neuwelt, CM ;
Brautbar, C ;
Gauderman, WJ ;
Jacob, CO .
HUMAN MOLECULAR GENETICS, 1999, 8 (04) :639-644
[79]   SAP increases FynT kinase activity and is required for phosphorylation of SLAM and Ly9 [J].
Simarro, M ;
Lanyi, A ;
Howie, D ;
Poy, F ;
Bruggeman, J ;
Choi, M ;
Sumegi, J ;
Eck, MJ ;
Terhorst, C .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (05) :727-736
[80]   PP59(FYN) MUTANT MICE DISPLAY DIFFERENTIAL SIGNALING IN THYMOCYTES AND PERIPHERAL T-CELLS [J].
STEIN, PL ;
LEE, HM ;
RICH, S ;
SORIANO, P .
CELL, 1992, 70 (05) :741-750