Known and potential functions for the SLP-76 adapter protein in regulating T-cell activation and development

被引:18
作者
Clements, JL [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Immunol, Buffalo, NY 14263 USA
关键词
D O I
10.1034/j.1600-065X.2003.00002.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The hematopoietic adapter protein SLP-76 is a critical component of multiple biochemical signaling 'circuits' in T cells that integrate proximal signaling events initiated by ligation of the T-cell receptor (TCR) into more distal pathways. Given the important role ascribed to TCR signaling in directing the outcome of thymocyte selection, it seems likely that SLP-76 may also function in signaling pathways that ultimately impact the establishment of the peripheral T-cell repertoire. It is generally accepted that the peripheral T-cell repertoire is selected in large part during T-cell development in the thymus. Molecular interactions between the TCR and self-peptide/major histocompatibility complexes expressed on thymic stromal elements dictate the fate of developing thymocytes. Thymocyte survival and further maturation (positive selection) require an active signal delivered to the cell as a consequence of TCR ligation. This raises the intriguing question of how a thymocyte can, for a narrow window of developmental time, obtain responsiveness to self while maintaining tolerance to these same determinants upon export to the periphery. This article reviews the current literature describing SLP-76-dependent signaling pathways in mature T cells and developing thymocytes. A potential role for this critical signaling intermediate in integrating signals leading to positive and negative selection of the peripheral T-cell repertoire is also discussed.
引用
收藏
页码:211 / 219
页数:9
相关论文
共 69 条
[1]   Induction of T helper type 2 immunity by a point mutation in the LAT adaptor [J].
Aguado, E ;
Richelme, S ;
Nuñez-Cruz, S ;
Miazek, A ;
Mura, AM ;
Richelme, M ;
Guo, XJ ;
Sainty, D ;
He, HT ;
Malissen, B ;
Malissen, M .
SCIENCE, 2002, 296 (5575) :2036-2040
[2]   Allelic exclusion of the T cell receptor β locus requires the SH2 domain-containing leukocyte protein (SLP)-76 adaptor protein [J].
Aifantis, I ;
Pivniouk, VI ;
Gärtner, F ;
Feinberg, J ;
Swat, W ;
Alt, FW ;
von Boehmer, H ;
Geha, RS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (08) :1093-1102
[3]   The Wiskott-Aldrich syndrome protein-interacting protein (WIP) binds to the adaptor protein Nck [J].
Anton, IM ;
Lu, WG ;
Mayer, BJ ;
Ramesh, N ;
Geha, RS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (33) :20992-20995
[4]   Recruitment of SLP-76 to the membrane and glycolipid-enriched membrane microdomains replaces the requirement for linker for activation of T cells in T cell receptor signaling [J].
Boerth, NJ ;
Sadler, JJ ;
Bauer, DE ;
Clements, JL ;
Gheith, SM ;
Koretzky, GA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) :1047-1058
[5]   Interaction of the Nck adapter protein with p21-activated kinase (PAK1) [J].
Bokoch, GM ;
Wang, Y ;
Bohl, BP ;
Sells, MA ;
Quilliam, LA ;
Knaus, UG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :25746-25749
[6]  
BUDAY L, 1994, J BIOL CHEM, V269, P9019
[7]   EPIDERMAL GROWTH-FACTOR REGULATES P21(RAS) THROUGH THE FORMATION OF A COMPLEX OF RECEPTOR, GRB2 ADAPTER PROTEIN, AND SOS NUCLEOTIDE EXCHANGE FACTOR [J].
BUDAY, L ;
DOWNWARD, J .
CELL, 1993, 73 (03) :611-620
[8]   Biochemical interactions integrating Itk with the T cell receptor-initiated signaling cascade [J].
Bunnell, SC ;
Diehn, M ;
Yaffe, MB ;
Findell, PR ;
Cantley, LC ;
Berg, LJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (03) :2219-2230
[9]   HUMAN SOS1 - A GUANINE-NUCLEOTIDE EXCHANGE FACTOR FOR RAS THAT BINDS TO GRB2 [J].
CHARDIN, P ;
CAMONIS, JH ;
GALE, NW ;
VANAELST, L ;
SCHLESSINGER, J ;
WIGLER, MH ;
BARSAGI, D .
SCIENCE, 1993, 260 (5112) :1338-1343
[10]  
Clements JL, 1998, J IMMUNOL, V161, P3880