Cellular interactions in thymocyte development

被引:389
作者
Anderson, G [1 ]
Moore, NC [1 ]
Owen, JJT [1 ]
Jenkinson, EJ [1 ]
机构
[1] UNIV BIRMINGHAM, SCH MED, CTR CLIN RES IMMUNOL & SIGNALLING, BIRMINGHAM B15 2TT, W MIDLANDS, ENGLAND
关键词
negative selection; positive selection; stroma; thymus; signaling;
D O I
10.1146/annurev.immunol.14.1.73
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interactions between stromal cells and thymocytes play a crucial role in T cell development. The thymic stroma is complex and consists of epithelial cells derived from the pharyngeal region during development, together with macrophages and dendritic cells of bone marrow origin. In addition, fibroblasts and matrix molecules permeate the whole framework. It is now apparent that these individual stromal components play specialized roles at different stages of T cell differentiation. Thus, at the early CD4(-)8(-) stage of development, T cell precursors require fibroblast as well as epithelial cell interactions. Later, at the CD4(+)8(+) stage, as well as providing low avidity TCR/MHC-peptide interactions, thymic epithelial cells have been shown to possess unique properties essential for positive selection. Dendritic cells, on the other hand, are probably efficient mediators of negative selection, but they may not be solely responsible for this activity. Alongside the functional roles of stromal cells, considerable progress is being made in unraveling the nature of the signaling pathways involved in T cell development. Identification of the pre-T cell receptor (pre-TCR) and associated signaling molecules marks an important advance in understanding the mechanisms that control gene rearrangement and allelic exclusion. In addition, a better understanding of the signaling pathways that lead to positive selection on the one hand and negative selection on the other is beginning to emerge. Many issues remain unresolved, and some are discussed in this review. What, for example, is the nature of the chemotactic factor(s) that attract stem cells to the thymus? What is the molecular basis of the essential interactions between early thymocytes and fibroblasts, and early thymocytes and epithelial cells? What is special about cortical epithelial cells in supporting positive selection? These and other issues are ripe for analysis and can now be approached using a combination of modern molecular and cellular techniques.
引用
收藏
页码:73 / 99
页数:27
相关论文
共 155 条
[1]   SELECTIVE REQUIREMENT FOR MAP KINASE ACTIVATION IN THYMOCYTE DIFFERENTIATION [J].
ALBEROLAILA, J ;
FORBUSH, KA ;
SEGER, R ;
KREBS, EG ;
PERLMUTTER, RM .
NATURE, 1995, 373 (6515) :620-623
[2]  
ANDERSON G, 1995, J IMMUNOL, V154, P3636
[3]   THYMIC EPITHELIAL-CELLS PROVIDE UNIQUE SIGNALS FOR POSITIVE SELECTION OF CD4+CD8+ THYMOCYTES IN-VITRO [J].
ANDERSON, G ;
OWEN, JJT ;
MOORE, NC ;
JENKINSON, EJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (06) :2027-2031
[4]   MHC CLASS-II-POSITIVE EPITHELIUM AND MESENCHYME CELLS ARE BOTH REQUIRED FOR T-CELL DEVELOPMENT IN THE THYMUS [J].
ANDERSON, G ;
JENKINSON, EJ ;
MOORE, NC ;
OWEN, JJT .
NATURE, 1993, 362 (6415) :70-73
[5]  
Anderson G, 1995, Semin Immunol, V7, P177, DOI 10.1016/1044-5323(95)90045-4
[6]   INHIBITION OF T-CELL RECEPTOR BETA-CHAIN GENE REARRANGEMENT BY OVEREXPRESSION OF THE NONRECEPTOR PROTEIN TYROSINE KINASE-P56LCK [J].
ANDERSON, SJ ;
ABRAHAM, KM ;
NAKAYAMA, T ;
SINGER, A ;
PERLMUTTER, RM .
EMBO JOURNAL, 1992, 11 (13) :4877-4886
[7]   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
[8]   THYMIC DENDRITIC CELLS AND T-CELLS DEVELOP SIMULTANEOUSLY IN THE THYMUS FROM A COMMON PRECURSOR POPULATION [J].
ARDAVIN, C ;
WU, L ;
LI, CL ;
SHORTMAN, K .
NATURE, 1993, 362 (6422) :761-763
[9]   DEFECTIVE T-CELL RECEPTOR SIGNALING AND CD8(+) THYMIC SELECTION IN HUMANS LACKING ZAP-70 KINASE [J].
ARPAIA, E ;
SHAHAR, M ;
DADI, H ;
COHEN, A ;
ROIFMAN, CM .
CELL, 1994, 76 (05) :947-958
[10]   EVIDENCE FOR A DIFFERENTIAL AVIDITY MODEL OF T-CELL SELECTION IN THE THYMUS [J].
ASHTONRICKARDT, PG ;
BANDEIRA, A ;
DELANEY, JR ;
VANKAER, L ;
PIRCHER, HP ;
ZINKERNAGEL, RM ;
TONEGAWA, S .
CELL, 1994, 76 (04) :651-663