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
[51]   Molecular and immunological basis of X-linked lymphoproliferative disease [J].
Latour, S ;
Veillette, A .
IMMUNOLOGICAL REVIEWS, 2003, 192 (01) :212-224
[52]   Binding of SAP SH2 domain to FynT SH3 domain reveals a novel mechanism of receptor signalling in immune regulation [J].
Latour, S ;
Roncagalli, R ;
Chen, RY ;
Bakinowski, M ;
Shi, XC ;
Schwartzberg, PL ;
Davidson, D ;
Veillette, A .
NATURE CELL BIOLOGY, 2003, 5 (02) :149-154
[53]   Regulation of SLAM-mediated signal transduction by SAP, the X-linked lymphoproliferative gene product [J].
Latour, S ;
Gish, G ;
Helgason, CD ;
Humphries, RK ;
Pawson, T ;
Veillette, A .
NATURE IMMUNOLOGY, 2001, 2 (08) :681-690
[54]   Requirement of homotypic NK-cell interactions through 2B4(CD244)/CD48 in the generation of NK effector functions [J].
Lee, KM ;
Forman, JP ;
McNerney, ME ;
Stepp, S ;
Kuppireddi, S ;
Guzior, D ;
Latchman, YE ;
Sayegh, MH ;
Yagita, H ;
Park, CK ;
Oh, SB ;
Wülfing, C ;
Schatzle, J ;
Mathew, PA ;
Sharpe, AH ;
Kumar, V .
BLOOD, 2006, 107 (08) :3181-3188
[55]   2B4 acts as a non-major histocompatibility complex binding inhibitory receptor on mouse natural killer cells [J].
Lee, KM ;
McNerney, ME ;
Stepp, SE ;
Mathew, PA ;
Schatzle, JD ;
Bennett, M ;
Kumar, V .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (09) :1245-1254
[56]   The SLAM-Associated protein signaling pathway is required for development of CD4+ T cells selected by homotypic thymocyte interaction [J].
Li, Wei ;
Sofi, M. Hanief ;
Rietdijk, Svend ;
Wang, Ninghai ;
Terhorst, Cox ;
Chang, Cheong-Hee .
IMMUNITY, 2007, 27 (05) :763-774
[57]   The flying height analysis of patterned sliders in magnetic hard disk drives [J].
Li, WL ;
Lee, SC ;
Chen, CW ;
Tsai, FR ;
Chen, MD ;
Chien, WT .
MICROSYSTEM TECHNOLOGIES-MICRO-AND NANOSYSTEMS-INFORMATION STORAGE AND PROCESSING SYSTEMS, 2005, 11 (01) :23-31
[58]   Regulation of cellular and humoral immune responses by the SLAM and SAP families of molecules [J].
Ma, Cindy S. ;
Nichols, Kim E. ;
Tangye, Stuart G. .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :337-379
[59]   Impaired humoral immunity in X-linked lymphoproliferative disease is associated with defective IL-10 production by CD4+ T cells [J].
Ma, CS ;
Hare, NJ ;
Nichols, KE ;
Dupré, L ;
Andolfi, G ;
Roncarolo, MG ;
Adelstein, S ;
Hodgkin, PD ;
Tangye, SG .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (04) :1049-1059
[60]   CD84 functions as a homophilic adhesion molecule and enhances IFN-γ secretion:: Adhesion is mediated by Ig-like domain 1 [J].
Martin, M ;
Romero, X ;
de la Fuente, MA ;
Tovar, V ;
Zapater, N ;
Esplugues, E ;
Pizcueta, P ;
Bosch, J ;
Engel, P .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3668-3676