Identification of self through two-dimensional chemistry and synapses

被引:128
作者
Dustin, ML
Bromley, SK
Davis, MM
Zhu, C
机构
[1] NYU, Sch Med, Skirball Inst Mol Med, New York, NY 10016 USA
[2] Washington Univ, Sch Med, Grad Program Immunol, St Louis, MO 63110 USA
[3] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[5] Georgia Inst Technol, Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[6] Georgia Inst Technol, Georgia Tech Emory Dept Biomed Engn, Atlanta, GA 30332 USA
关键词
affinity; kinetics; adhesion; T cell activation; synapses;
D O I
10.1146/annurev.cellbio.17.1.133
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cells in the immune and nervous systems communicate through informational synapses. The two-dimensional chemistry underlying the process of synapse formation is beginning to be explored using fluorescence imaging and mechanical techniques. Early analysis of two-dimensional kinetic rates (k(on) and k(off)) and equilibrium constants (K-d) provides a number of biological insights. First, there are two regimes for adhesion-one disordered with slow k(on) and the other self-ordered with 10(4)-fold faster k(on). Despite huge variation in two-dimensional k(on), the two-dimensional k(off) is like k(off) in solution, and two-dimensional k(off) is more closely related to intrinsic properties of the interaction than the two-dimensional k(on). Thus difference in k(off) can be used to set signaling thresholds. Early signaling complexes are compartmentalized to generate synergistic signaling domains. Immune antigen receptor components have a role in neural synapse editing. This suggests significant parallels in informational synapse formation based on common two-dimensional chemistry and signaling strategies.
引用
收藏
页码:133 / 157
页数:27
相关论文
共 114 条
[41]   Functional requirement for class I MHC in CNS development and plasticity [J].
Huh, GS ;
Boulanger, LM ;
Du, HP ;
Riquelme, PA ;
Brotz, TM ;
Shatz, CJ .
SCIENCE, 2000, 290 (5499) :2155-2159
[42]   CD45 is a JAK phosphatase and negatively regulates cytokine receptor signalling [J].
Irie-Sasaki, J ;
Sasaki, T ;
Matsumoto, W ;
Opavsky, A ;
Cheng, M ;
Welstead, G ;
Griffiths, E ;
Krawczyk, C ;
Richardson, CD ;
Aitken, K ;
Iscove, N ;
Koretzky, G ;
Johnson, P ;
Liu, P ;
Rothstein, DM ;
Penninger, JM .
NATURE, 2001, 409 (6818) :349-354
[43]  
IZZARD CS, 1976, J CELL SCI, V21, P129
[44]   A supramolecular basis for CD45 tyrosine phosphatase regulation in sustained T cell activation [J].
Johnson, KG ;
Bromley, SK ;
Dustin, ML ;
Thomas, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (18) :10138-10143
[45]  
Johnson KG, 1999, J IMMUNOL, V162, P3802
[46]   GRANULOCYTE ENDOTHELIUM INITIAL ADHESION - ANALYSIS OF TRANSIENT BINDING EVENTS MEDIATED BY E-SELECTIN IN A LAMINAR SHEAR-FLOW [J].
KAPLANSKI, G ;
FARNARIER, C ;
TISSOT, O ;
PIERRES, A ;
BENOLIEL, AM ;
ALESSI, MC ;
KAPLANSKI, S ;
BONGRAND, P .
BIOPHYSICAL JOURNAL, 1993, 64 (06) :1922-1933
[47]   Rap1 is a potent activation signal for leukocyte function-associated antigen 1 distinct from protein kinase C and phosphatidylinositol-3-OH kinase [J].
Katagiri, K ;
Hattori, M ;
Minato, N ;
Irie, S ;
Takatsu, K ;
Kinashi, T .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (06) :1956-1969
[48]   Fidelity of T cell activation through multistep T cell receptor ζ phosphorylation [J].
Kersh, EN ;
Shaw, AS ;
Allen, PM .
SCIENCE, 1998, 281 (5376) :572-575
[49]   High- and low-potency ligands with similar affinities for the TCR: The importance of kinetics in TCR signaling [J].
Kersh, GJ ;
Kersh, EN ;
Fremont, DH ;
Allen, PM .
IMMUNITY, 1998, 9 (06) :817-826
[50]   MHC CLASS-II INTERACTION WITH CD4 MEDIATED BY A REGION ANALOGOUS TO THE MHC CLASS-I BINDING-SITE FOR CD8 [J].
KONIG, R ;
HUANG, LY ;
GERMAIN, RN .
NATURE, 1992, 356 (6372) :796-798