The Dendritic Cell Synapse: A Life Dedicated to T Cell Activation

被引:62
作者
Benvenuti, Federica [1 ]
机构
[1] Int Ctr Genet Engn & Biotechnol, Cellular Immunol, Padriciano 99, I-34012 Trieste, Italy
关键词
immune synapse; dendritic cells; actin cytoskeleton; polarized secretion; antigen presentation; ALDRICH-SYNDROME PROTEIN; II MHC COMPARTMENTS; IMMUNOLOGICAL SYNAPSE; IMMUNE SYNAPSE; CUTTING EDGE; RECEPTOR; POLARIZATION; ADHESION; LYMPHOCYTES; EXPRESSION;
D O I
10.3389/fimmu.2016.00070
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell activation within immunological synapses is a complex process whereby different types of signals are transmitted from antigen-presenting cells to T cells. The molecular strategies developed by T cells to interpret and integrate these signals have been systematically dissected in recent years and are now in large part understood. On the other side of the immune synapse, dendritic cells (DCs) participate actively in synapse formation and maintenance by remodeling of membrane receptors and intracellular content. However, the details of such changes have been only partially characterized. The DCs actin cytoskeleton has been one of the first systems to be identified as playing an important role in T-cell priming and some of the underlying mechanisms have been elucidated. Similarly, the DCs microtubule cytoskeleton undergoes major spatial changes during synapse formation that favor polarization of the DCs subcellular space toward the interacting T cell. Recently, we have begun to investigate the trafficking machinery that controls polarized delivery of endosomal vesicles at the DC-T immune synapse with the aim of understanding the functional relevance of polarized secretion of soluble factors during T-cell priming. Here, we will review the current knowledge of events occurring in DCs during synapse formation and discuss the open questions that still remain unanswered.
引用
收藏
页数:6
相关论文
共 55 条
[1]   Fascin is involved in the antigen presentation activity of mature dendritic cells [J].
Al-Alwan, MM ;
Rowden, G ;
Lee, TDG ;
West, KA .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :338-345
[2]   Cutting edge: The dendritic cell cytoskeleton is critical for the formation of the immunological synapse [J].
Al-Alwan, MM ;
Rowden, G ;
Lee, TDG ;
West, KA .
JOURNAL OF IMMUNOLOGY, 2001, 166 (03) :1452-1456
[3]   Requirement of Rac1 and Rac2 expression by mature dendritic cells for T cell priming [J].
Benvenuti, F ;
Hugues, S ;
Walmsley, M ;
Ruf, S ;
Fetler, L ;
Popoff, M ;
Tybulewicz, VLJ ;
Amigorena, S .
SCIENCE, 2004, 305 (5687) :1150-1153
[4]   Dendritic cell maturation controls adhesion, synapse formation, and the duration of the interactions with naive T lymphocytes [J].
Benvenuti, F ;
Lagaudrière-Gesbert, C ;
Grandjean, I ;
Jancic, C ;
Hivroz, C ;
Trautmann, A ;
Lantz, O ;
Amigorena, S .
JOURNAL OF IMMUNOLOGY, 2004, 172 (01) :292-301
[5]   Spinophilin participates in information transfer at immunological synapses [J].
Bloom, Ona ;
Unternaehrer, Julia J. ;
Jiang, Aimin ;
Shin, Jeong-Sook ;
Delamarre, Lelia ;
Allen, Patrick ;
Mellman, Ira .
JOURNAL OF CELL BIOLOGY, 2008, 181 (02) :203-211
[6]   T cells induce extended class II MHC compartments in dendritic cells in a toll-like receptor-dependent manner [J].
Boes, M ;
Bertho, N ;
Cerny, J ;
den Brouw, MO ;
Kirchhausen, T ;
Ploegh, H .
JOURNAL OF IMMUNOLOGY, 2003, 171 (08) :4081-4088
[7]   T-cell engagement of dendritic cells rapidly rearranges MHC class II transport [J].
Boes, M ;
Cerny, J ;
Massol, R ;
Op den Brouw, M ;
Kirchhausen, T ;
Chen, JZ ;
Ploegh, HL .
NATURE, 2002, 418 (6901) :983-988
[8]   Immunological synapse formation licenses CD40-CD40L accumulations at T-APC contact sites [J].
Boisvert, J ;
Edmondson, S ;
Krummel, MF .
JOURNAL OF IMMUNOLOGY, 2004, 173 (06) :3647-3652
[9]   NK cell activation by dendritic cells (DCs) requires the formation of a synapse leading to IL-12 polarization in DCs [J].
Borg, C ;
Jalil, A ;
Laderach, D ;
Maruyama, K ;
Wakasugi, H ;
Charrier, S ;
Ryffel, B ;
Cambi, A ;
Figdor, C ;
Vainchenker, W ;
Galy, A ;
Caignard, A ;
Zitvogel, L .
BLOOD, 2004, 104 (10) :3267-3275
[10]   Cytoskeletal remodeling mediated by WASp in dendritic cells is necessary for normal immune synapse formation and T-cell priming [J].
Bouma, Gerben ;
Mendoza-Naranjo, Ariadna ;
Blundell, Michael P. ;
de Falco, Elena ;
Parsley, Kathryn L. ;
Burns, Siobhan O. ;
Thrasher, Adrian J. .
BLOOD, 2011, 118 (09) :2492-2501