TOX: an HMG box protein implicated in the regulation of thymocyte selection

被引:156
作者
Wilkinson, B [1 ]
Chen, JYF [1 ]
Han, P [1 ]
Rufner, KM [1 ]
Goularte, OD [1 ]
Kaye, J [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.1038/ni767
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the thymus, pre-T cell receptor (pre-TCR)-mediated signaling and then TCR-mediated signaling initiate changes in gene expression that result in the maturation of CD4 and CD8 lineage T cells from common precursors. Using gene chip technology, we isolated a murine gene, designated Tox, that encodes a member of the HMG (high-mobility group) box family of DNA-binding proteins. TOX expression is up-regulated by both pre-TCR and TCR activation of immature thymocytes but not by TCR activation of mature naive T cells. Transgenic mice that express TOX show expanded CD8(+) and reduced CD4(+) single positive thymocyte subpopulations. We present evidence here that this phenotype results from a perturbation in lineage commitment due to reduced sensitivity to TCR-mediated signaling. This molecular marker of thymic selection events may therefore play a role in establishing the activation threshold of developing T cells and patterning changes in gene expression.
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收藏
页码:272 / 280
页数:9
相关论文
共 62 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Ikaros sets thresholds for T cell activation and regulates chromosome propagation [J].
Avitahl, N ;
Winandy, S ;
Friedrich, C ;
Jones, B ;
Ge, YM ;
Georgopoulos, K .
IMMUNITY, 1999, 10 (03) :333-343
[3]   CD5 expression is developmentally regulated by T cell receptor (TCR) signals and TCR avidity [J].
Azzam, HS ;
Grinberg, A ;
Lui, K ;
Shen, H ;
Shores, EW ;
Love, PE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2301-2311
[4]   Fine tuning of TCR signaling by CD5 [J].
Azzam, HS ;
DeJarnette, JB ;
Huang, K ;
Emmons, R ;
Park, CS ;
Sommers, CL ;
El-Khoury, D ;
Shores, EW ;
Love, PE .
JOURNAL OF IMMUNOLOGY, 2001, 166 (09) :5464-5472
[5]   The CD4/CD8 lineage decision: integration of signalling pathways [J].
Basson, MA ;
Zamoyska, R .
IMMUNOLOGY TODAY, 2000, 21 (10) :509-514
[6]   Flexing DNA: HMG-box proteins and their partners [J].
Bianchi, ME ;
Beltrame, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (06) :1573-1577
[7]   Coreceptor reversal in the thymus:: Signaled CD4+8+ thymocytes initially terminate CD8 transcription even when differentiating into CD8+ T cells [J].
Brugnera, E ;
Bhandoola, A ;
Cibotti, R ;
Yu, Q ;
Guinter, TI ;
Yamashita, Y ;
Sharrow, SO ;
Singer, A .
IMMUNITY, 2000, 13 (01) :59-71
[8]   DISSECTION OF THYMOCYTE SIGNALING PATHWAYS BY INVIVO EXPRESSION OF PERTUSSIS TOXIN ADP-RIBOSYLTRANSFERASE [J].
CHAFFIN, KE ;
BEALS, CR ;
WILKIE, TM ;
FORBUSH, KA ;
SIMON, MI ;
PERLMUTTER, RM .
EMBO JOURNAL, 1990, 9 (12) :3821-3829
[9]   Correlating notch signaling with thymocyte maturation [J].
Deftos, ML ;
He, YW ;
Ojala, EW ;
Bevan, MJ .
IMMUNITY, 1998, 9 (06) :777-786
[10]  
DUTZ JP, 1995, J IMMUNOL, V154, P2588