The bHLH gene Hes1 is essential for expansion of early T cell precursors

被引:187
作者
Tomita, K
Hattori, M [1 ]
Nakamura, E
Nakanishi, S
Minato, N
Kageyama, R
机构
[1] Kyoto Univ, Inst Virus Res, Kyoto 6068507, Japan
[2] Kyoto Univ, Fac Med, Dept Biol Sci, Kyoto 6068501, Japan
[3] Kyoto Univ, Fac Med, Dept Immunol & Cell Biol, Kyoto 6068501, Japan
关键词
bHLH; Hes1; T cell; thymocyte; thymus;
D O I
10.1101/gad.13.9.1203
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mice mutant for the bHLH gene Hes1, which is known to keep cells in a proliferative state, mostly lack thymus. Transfer of Hes1-null fetal liver cells into RAG2-null host mice normally reconstitutes B cells but fails to generate mature T cells in the thymus. In the reconstituted thymus, T cell differentiation is arrested at the CD4(-)CD8(-) double negative (DN) stage. Both the initial T cell receptor (TCR)-independent and the subsequent TCR-dependent selective expansion during the DN stage are severely affected. Thus, Hes1 is essential for the earliest thymocyte expansion in a cell-autonomous manner.
引用
收藏
页码:1203 / 1210
页数:8
相关论文
共 29 条
[1]   Cellular interactions in thymocyte development [J].
Anderson, G ;
Moore, NC ;
Owen, JJT ;
Jenkinson, EJ .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :73-99
[2]   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
[3]   IL-7 receptor and VDJ recombination: Trophic versus mechanistic actions [J].
Candeias, S ;
Muegge, K ;
Durum, SK .
IMMUNITY, 1997, 6 (05) :501-508
[4]   Conservation of the Drosophila lateral inhibition pathway in human lung cancer: A hairy-related protein (HES-1) directly represses achaete-scute homolog-1 expression [J].
Chen, H ;
Thiagalingam, A ;
Chopra, H ;
Borges, MW ;
Feder, JN ;
Nelkin, BD ;
Baylin, SB ;
Ball, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5355-5360
[5]  
GODFREY DI, 1994, J IMMUNOL, V152, P4783
[6]  
GODFREY DI, 1993, J IMMUNOL, V150, P4244
[7]   CONTROL POINTS IN EARLY T-CELL DEVELOPMENT [J].
GODFREY, DI ;
ZLOTNIK, A .
IMMUNOLOGY TODAY, 1993, 14 (11) :547-553
[8]   A DEVELOPMENTAL SWITCH IN THYMIC LYMPHOCYTE MATURATION POTENTIAL OCCURS AT THE LEVEL OF HEMATOPOIETIC STEM-CELLS [J].
IKUTA, K ;
KINA, T ;
MACNEIL, I ;
UCHIDA, N ;
PEAULT, B ;
CHIEN, YH ;
WEISSMAN, IL .
CELL, 1990, 62 (05) :863-874
[9]   PERSISTENT EXPRESSION OF HELIX-LOOP-HELIX FACTOR HES-1 PREVENTS MAMMALIAN NEURAL DIFFERENTIATION IN THE CENTRAL-NERVOUS-SYSTEM [J].
ISHIBASHI, M ;
MORIYOSHI, K ;
SASAI, Y ;
SHIOTA, K ;
NAKANISHI, S ;
KAGEYAMA, R .
EMBO JOURNAL, 1994, 13 (08) :1799-1805
[10]   Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects [J].
Ishibashi, M ;
Ang, SL ;
Shiota, K ;
Nakanishi, S ;
Kageyama, R ;
Guillemot, F .
GENES & DEVELOPMENT, 1995, 9 (24) :3136-3148