Sin: good or bad? A T lymphocyte perspective

被引:20
作者
Alexandropoulos, K
Donlin, LT
Xing, LZ
Regelmann, AG
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pharmacol, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Integrated Program, New York, NY 10032 USA
关键词
D O I
10.1034/j.1600-065X.2003.00021.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
Stimulation of T cells through their antigen receptor induces a multitude of signaling networks that regulate T cell activation in the form of cytokine production and T cell proliferation. Multiple signal integration sites exist along these pathways in the form of multiprotein signaling complexes, the formation of which is facilitated by adapter and scaffold molecules. In recent years a number of adapter and scaffold molecules have been described in T cells and shown to play an integral part in T cell function. Among these molecules are proteins that function as positive or negative regulators of T cell activation downstream of the activated T cell receptor (TCR). Here, we discuss the role of a small family of multiadapter proteins on T cell activation, the p130Cas family, with emphasis on one of its members, Sin (Src-interacting protein). Our results suggest that Sin inhibits thymocyte development and T cell activation and is a novel negative regulator of T lymphocyte function.
引用
收藏
页码:181 / 195
页数:15
相关论文
共 91 条
[1]   PROLINE-RICH SEQUENCES THAT BIND TO SRC HOMOLOGY-3 DOMAINS WITH INDIVIDUAL SPECIFICITIES [J].
ALEXANDROPOULOS, K ;
CHENG, GH ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3110-3114
[2]   Coordinate activation of c-Src by SH3- and SH2-binding sites on a novel, p130(Cas)-related protein, Sin [J].
Alexandropoulos, K ;
Baltimore, D .
GENES & DEVELOPMENT, 1996, 10 (11) :1341-1355
[3]   DEFECTIVE T-CELL RECEPTOR SIGNALING IN MICE LACKING THE THYMIC ISOFORM OF P59(FYN) [J].
APPLEBY, MW ;
GROSS, JA ;
COOKE, MP ;
LEVIN, SD ;
QIAN, X ;
PERLMUTTER, RM .
CELL, 1992, 70 (05) :751-763
[4]   Grf40, a novel Grb2 family member, is involved in T cell signaling through interaction with SLP-76 and LAT [J].
Asada, H ;
Ishii, N ;
Sasaki, Y ;
Endo, K ;
Kasai, H ;
Tanaka, N ;
Takeshita, T ;
Tsuchiya, S ;
Konno, T ;
Sugamura, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (09) :1383-1390
[5]   Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b [J].
Bachmaier, K ;
Krawczyk, C ;
Kozieradzki, I ;
Kong, YY ;
Sasaki, T ;
Oliveira-dos-Santos, A ;
Mariathasan, S ;
Bouchard, D ;
Wakeham, A ;
Itie, A ;
Le, J ;
Ohashi, PS ;
Sarosi, I ;
Nishina, H ;
Lipkowitz, S ;
Penninger, JM .
NATURE, 2000, 403 (6766) :211-216
[6]   Mona, a novel hematopoietic-specific adaptor interacting with the macrophage colony-stimulating factor receptor, is implicated in monocyte/macrophage development [J].
Bourette, RP ;
Arnaud, S ;
Myles, GM ;
Blanchet, JP ;
Rohrschneider, LR ;
Mouchiroud, G .
EMBO JOURNAL, 1998, 17 (24) :7273-7281
[7]   Maintenance of human T cell anergy: Blocking of IL-2 gene transcription by activated Rap1 [J].
Boussiotis, VA ;
Freeman, GJ ;
Berezovskaya, A ;
Barber, DL ;
Nadler, LM .
SCIENCE, 1997, 278 (5335) :124-128
[8]   Phosphoprotein associated with glycosphingolipid-enriched microdomains (PAG), a novel ubiquitously expressed transmembrane adaptor protein, binds the protein tyrosine kinase Csk and is involved in regulation of T cell activation [J].
Brdicka, T ;
Pavilstová, D ;
Leo, A ;
Bruyns, E ;
Korínek, V ;
Angelisová, P ;
Scherer, J ;
Shevchenko, A ;
Shevchenko, A ;
Hilgert, I ;
Cerny, J ;
Drbal, K ;
Kuramitsu, Y ;
Kornacker, B ;
Horejsí, V ;
Schraven, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (09) :1591-1604
[9]   Signal transduction: hanging on a scaffold [J].
Burack, WR ;
Shaw, AS .
CURRENT OPINION IN CELL BIOLOGY, 2000, 12 (02) :211-216
[10]   Scaffolds, adaptors and linkers of TCR signaling: theory and practice [J].
Burack, WR ;
Cheng, AM ;
Shaw, AS .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (03) :312-316