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
[1]   The kinetics of L-selectin tethers and the mechanics of selectin-mediated rolling [J].
Alon, R ;
Chen, SQ ;
Puri, KD ;
Finger, EB ;
Springer, TA .
JOURNAL OF CELL BIOLOGY, 1997, 138 (05) :1169-1180
[2]   LIFETIME OF THE P-SELECTIN-CARBOHYDRATE BOND AND ITS RESPONSE TO TENSILE FORCE IN HYDRODYNAMIC FLOW [J].
ALON, R ;
HAMMER, DA ;
SPRINGER, TA .
NATURE, 1995, 374 (6522) :539-542
[3]   Concentration of MHC class II molecules in lipid rafts facilitates antigen presentation [J].
Anderson, HA ;
Hiltbold, EM ;
Roche, PA .
NATURE IMMUNOLOGY, 2000, 1 (02) :156-162
[4]   T cell differentiation: a mechanistic view [J].
Avni, O ;
Rao, A .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (06) :654-659
[5]   CELL-ADHESION - COMPETITION BETWEEN NONSPECIFIC REPULSION AND SPECIFIC BONDING [J].
BELL, GI ;
DEMBO, M ;
BONGRAND, P .
BIOPHYSICAL JOURNAL, 1984, 45 (06) :1051-1064
[6]  
BELL GI, 1978, SCIENCE, V200, P618, DOI 10.1126/science.347575
[7]   ALPHA-4 INTEGRINS MEDIATE LYMPHOCYTE ATTACHMENT AND ROLLING UNDER PHYSIOLOGICAL FLOW [J].
BERLIN, C ;
BARGATZE, RF ;
CAMPBELL, JJ ;
VONANDRIAN, UH ;
SZABO, MC ;
HASSLEN, SR ;
NELSON, RD ;
BERG, EL ;
ERLANDSEN, SL ;
BUTCHER, EC .
CELL, 1995, 80 (03) :413-422
[8]   Integrin LFA-1 interacts with the transcriptional co-activator JAB1 to modulate AP-1 activity [J].
Bianchi, E ;
Denti, S ;
Granata, A ;
Bossi, G ;
Geginat, J ;
Villa, A ;
Rogge, L ;
Pardi, R .
NATURE, 2000, 404 (6778) :617-+
[9]   Sequential involvement of Lck and SHP-1 with MHC-recognizing receptors on NK cells inhibits FcR-initiated tyrosine kinase activation [J].
Binstadt, BA ;
Brumbaugh, KM ;
Dick, CJ ;
Scharenberg, AM ;
Williams, BL ;
Colonna, M ;
Lanier, LL ;
Kinet, JP ;
Abraham, RT ;
Leibson, PJ .
IMMUNITY, 1996, 5 (06) :629-638
[10]   Thermodynamics of T cell receptor binding to peptide-MHC: Evidence for a general mechanism of molecular scanning [J].
Boniface, JJ ;
Reich, Z ;
Lyons, DS ;
Davis, MM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11446-11451