Regulation of T cell development in the thymus

被引:17
作者
Kaye, J [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
T cell development; thymus; thymocyte; T cell receptor; Ras; mitogen-activated protein kinase; gene expression;
D O I
10.1385/IR:21:2-3:71
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
My colleagues and I are studying the regulation of T cell differentiation and lineage commitment in the thymus. Most recently, we have focused on the role of the mitogen-activated protein kinase (MAPK) signaling pathway in these processes and, in particular, the temporal pattern of activation of this pathway and its effect on downstream gene targets. Our data suggest that thymocyte differentiation to either the CD4 or CD8 lineages requires sustained low-level signaling via MAPK, although the latter requires a weaker signal. We have proposed that both the amplitude and kinetics of MAPK signaling may be one aspect of the link between T cell receptor affinity and cell fate. In addition, we have shown that the Egr family of transcription factors is induced as a consequence of MAPK activation during positive selection in the thymus, and we are taking several approaches to identify other genes that are involved in regulating this developmental process.
引用
收藏
页码:71 / 81
页数:11
相关论文
共 39 条
[1]   T-cell-receptor affinity and thymocyte positive selection [J].
Alam, SM ;
Travers, PJ ;
Wung, JL ;
Nasholds, W ;
Redpath, S ;
Jameson, SC ;
Gascoigne, NRJ .
NATURE, 1996, 381 (6583) :616-620
[2]   Positive and negative selection invoke distinct signaling pathways [J].
AlberolaIla, J ;
Hogquist, KA ;
Swan, KA ;
Bevan, MJ ;
Perlmutter, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (01) :9-18
[3]   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
[4]   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
[5]  
Bommhardt U, 1999, J IMMUNOL, V163, P715
[6]   Cell survival promoted by the Ras-MAPK signaling pathway by transcription-dependent and -independent mechanisms [J].
Bonni, A ;
Brunet, A ;
West, AE ;
Datta, SR ;
Takasu, MA ;
Greenberg, ME .
SCIENCE, 1999, 286 (5443) :1358-1362
[7]   T cell antigen receptor signal transduction pathways [J].
Cantrell, D .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :259-274
[8]   IDENTIFICATION AND CHARACTERIZATION OF THE EGR-1 GENE-PRODUCT, A DNA-BINDING ZINC FINGER PROTEIN-INDUCED BY DIFFERENTIATION AND GROWTH SIGNALS [J].
CAO, XM ;
KOSKI, RA ;
GASHLER, A ;
MCKIERNAN, M ;
MORRIS, CF ;
GAFFNEY, R ;
HAY, RV ;
SUKHATME, VP .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (05) :1931-1939
[9]   BIOLOGICAL AND BIOCHEMICAL-PROPERTIES OF HUMAN RASH GENES MUTATED AT CODON-61 [J].
DER, CJ ;
FINKEL, T ;
COOPER, GM .
CELL, 1986, 44 (01) :167-176
[10]   STIMULATION OF P21RAS UPON T-CELL ACTIVATION [J].
DOWNWARD, J ;
GRAVES, JD ;
WARNE, PH ;
RAYTER, S ;
CANTRELL, DA .
NATURE, 1990, 346 (6286) :719-723