SLP76 and SLP65: complex regulation of signalling in lymphocytes and beyond

被引:214
作者
Koretzky, GA [1 ]
Abtahian, F [1 ]
Silverman, MA [1 ]
机构
[1] Univ Penn, Abramson Family Canc Res Inst, Dept Med, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
D O I
10.1038/nri1750
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
SLP76 and SLP65 are adaptor proteins that lack intrinsic enzymatic activity but contain multiple protein-binding domains. These proteins are essential for signalling downstream of integrins and receptors that contain immunoreceptor tyrosine-based activation motifs. The absence of these adaptor proteins profoundly affects various lineages in the haematopoietic compartment and severely compromises vascular development, highlighting their importance as regulators of signalling cascades. In this Review, we discuss the role of SLP76 and SLP65 in several signalling pathways in haematopoietic cells, with an emphasis on recent studies that provide insight into their mechanisms of action.
引用
收藏
页码:67 / 78
页数:12
相关论文
共 134 条
[1]   Timeline - Jurkat T cells and development of the T-cell receptor signalling paradigm [J].
Abraham, RT ;
Weiss, A .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (04) :301-308
[2]   Regulation of blood and lymphatic vascular separation by signaling proteins SLP-76 and Syk [J].
Abtahian, F ;
Guerriero, A ;
Sebzda, E ;
Lu, MM ;
Zhou, R ;
Mocsai, A ;
Myers, EE ;
Huang, B ;
Jackson, DG ;
Ferrari, VA ;
Tybulewicz, V ;
Lowell, CA ;
Lepore, JJ ;
Koretzky, GA ;
Kahn, ML .
SCIENCE, 2003, 299 (5604) :247-251
[3]   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
[4]   A high-affinity Arg-X-X-Lys SH3 binding motif confers specificity for the interaction between gads and SLP-76 in T cell signaling [J].
Berry, DM ;
Nash, P ;
Liu, SKW ;
Pawson, T ;
McGlade, CJ .
CURRENT BIOLOGY, 2002, 12 (15) :1336-1341
[5]  
Berton G, 1999, Curr Opin Hematol, V6, P51, DOI 10.1097/00062752-199901000-00009
[6]   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
[7]   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
[8]   Adapter proteins SLP-76 and BLNK both are expressed by murine macrophages and are linked to signaling via Fcγ receptors I and II/III [J].
Bonilla, FA ;
Fujita, RM ;
Pivniouk, VI ;
Chan, AC ;
Geha, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1725-1730
[9]   Non-T cell activation linker (NTAL):: A transmembrane adaptor protein involved in immunoreceptor signaling [J].
Brdicka, T ;
Imrich, M ;
Angelisová, P ;
Brdicková, N ;
Horváth, O ;
Spicka, J ;
Hilgert, I ;
Lusková, P ;
Dráber, P ;
Novák, P ;
Engels, N ;
Wienands, J ;
Simeoni, L ;
Österreicher, J ;
Aguado, E ;
Malissen, M ;
Schraven, B ;
Horejsí, V .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (12) :1617-1626
[10]   T cell receptor ligation induces the formation of dynamically regulated signaling assemblies [J].
Bunnell, SC ;
Hong, DI ;
Kardon, JR ;
Yamazaki, T ;
McGlade, CJ ;
Barr, VA ;
Samelson, LE .
JOURNAL OF CELL BIOLOGY, 2002, 158 (07) :1263-1275