New views of the immunological synapse: variations in assembly and function

被引:45
作者
Jacobelli, J [1 ]
Andres, PG [1 ]
Boisvert, J [1 ]
Krummel, MF [1 ]
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.coi.2004.03.008
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 interaction of T cells with antigen-presenting cells results in the formation of a contact face, termed the immunological synapse. The prototypical dynamics of this process are well established and involve cessation of crawling, a highly fluid 'immature' synapse phase during which signaling is initiated, and ultimately the formation of a 'mature' synapse characterized by centralized and peripheral supramolecular activating complexes. Ongoing research is directed towards defining how these supramolecular assemblies are formed and, more importantly, to what end. With regard to the former, progress has been made in defining the order in which various molecules are recruited to signaling centers in prototypical settings. With regard to the latter, however, the issue now appears more complex, as both developmental changes in T cells and variations in the environment appear to modulate features of mature synapse development. Although many details of the immunological synapse have been established, emerging evidence suggests a great variability in the ultimate form of these contacts and their effects on T-cell functions.
引用
收藏
页码:345 / 352
页数:8
相关论文
共 52 条
[1]  
ANDRES PG, 2004, IN PRESS J IMMUNOL
[2]   The Wiskott-Aldrich syndrome protein acts downstream of CD2 and the CD2AP and PSTPIP1 adaptors to promote formation of the immunological synapse [J].
Badour, K ;
Zhang, JY ;
Shi, F ;
McGavin, MKH ;
Rampersad, V ;
Hardy, LA ;
Field, D ;
Siminovitch, KA .
IMMUNITY, 2003, 18 (01) :141-154
[3]  
BOOTMAN MD, 1998, CELL, P367
[4]   Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes [J].
Bousso, P ;
Robey, E .
NATURE IMMUNOLOGY, 2003, 4 (06) :579-585
[5]   Cutting edge: Hierarchy of chemokine receptor and TCR signals regulating T cell migration and proliferation [J].
Bromley, SK ;
Peterson, DA ;
Gunn, MD ;
Dustin, ML .
JOURNAL OF IMMUNOLOGY, 2000, 165 (01) :15-19
[6]   The immunological synapse and CD28-CD80 interactions [J].
Bromley, SK ;
Iaboni, A ;
Davis, SJ ;
Whitty, A ;
Green, JM ;
Shaw, AS ;
Weiss, A ;
Dustin, ML .
NATURE IMMUNOLOGY, 2001, 2 (12) :1159-1166
[7]   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
[8]   Quantitative imaging of raft accumulation in the immunological synapse [J].
Burack, WR ;
Lee, KH ;
Holdorf, AD ;
Dustin, ML ;
Shaw, AS .
JOURNAL OF IMMUNOLOGY, 2002, 169 (06) :2837-2841
[9]   Negative regulation of T cell receptor-lipid raft interaction by cytotoxic T lymphocyte-associated antigen 4 [J].
Chikuma, S ;
Imboden, JB ;
Bluestone, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (01) :129-135
[10]   Surface cytotoxic T lymphocyte-associated antigen 4 partitions within lipid rafts and relocates to the immunological synapse under conditions of inhibition of T cell activation [J].
Darlington, PJ ;
Baroja, ML ;
Chau, TA ;
Siu, E ;
Ling, V ;
Carreno, BM ;
Madrenas, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 195 (10) :1337-1347