Hlx is induced by and genetically interacts with T-bet to promote heritable TH1 gene induction

被引:0
|
作者
Alan C. Mullen
Anne S. Hutchins
Frances A. High
Hubert W. Lee
Kara J. Sykes
Lewis A. Chodosh
Steven L. Reiner
机构
[1] University of Pennsylvania,Abramson Family Cancer Research Institute and Department of Medicine
来源
Nature Immunology | 2002年 / 3卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
Type 1 helper T (TH1) cells are essential for cellular immunity, but their ontogeny, maturation and durability remain poorly understood. By constructing a dominant-negative form of T-bet, we were able to determine the role played by this lineage-inducing trans-activator in the establishment and maintenance of heritable TH1 gene expression. Optimal induction of interferon-γ (IFN-γ) expression required genetic interaction between T-bet and its target, the homeoprotein Hlx. In fully mature TH1 cells, reiteration of IFN-γ expression and stable chromatin remodeling became relatively independent of T-bet activity and coincided with demethylation of DNA. In contrast, some lineage attributes, such as expression of IL-12Rβ2 (interleukin 12 receptor β2), required ongoing T-bet activity in mature TH1 cells and their progeny. These findings suggest that heritable states of gene expression might be maintained by continued expression of the inducing factor or by a mechanism that confers a stable imprint of the induced state.
引用
收藏
页码:652 / 658
页数:6
相关论文
共 50 条
  • [21] Overexpression of T-bet in T cells accelerates autoimmune glomerulonephritis in mice with a dominant Th1 background
    Shimohata, Homare
    Yamada, Akiko
    Yoh, Keigyou
    Ishizaki, Kazusa
    Morito, Naoki
    Yamagata, Kunihiro
    Takahashi, Satoru
    JOURNAL OF NEPHROLOGY, 2009, 22 (01) : 123 - 129
  • [22] Early growth response gene (Egr) 2 and 3 control Th1 differentiation by directly inhibiting T-bet
    Miao, T.
    Li, S.
    Symonds, A.
    Wang, P.
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2016, 46 : 524 - 524
  • [23] T-bet upregulation and subsequent interleukin 12 stimulation are essential for induction of Th1 mediated immunopathology in Crohn's disease
    Matsuoka, K
    Inoue, N
    Sato, T
    Okamoto, S
    Hisamatsu, T
    Kishi, Y
    Sakuraba, A
    Hitotsumatsu, O
    Ogata, H
    Koganei, K
    Fukushima, T
    Kanai, T
    Watanabe, M
    Ishii, H
    Hibi, T
    GUT, 2004, 53 (09) : 1303 - 1308
  • [24] Regulation of the Th1 Genomic Locus from Ifng through Tmevpg1 by T-bet
    Collier, Sarah P.
    Henderson, Melodie A.
    Tossberg, John T.
    Aune, Thomas M.
    JOURNAL OF IMMUNOLOGY, 2014, 193 (08): : 3959 - 3965
  • [25] 转录因子T-bet与Th1/Th2及哮喘的关系
    李杰
    王志强
    生物技术通报, 2010, (07) : 55 - 58
  • [26] T-bet and Eomesodermin Play Critical Roles in Directing T Cell Differentiation to Th1 versus Th17
    Yang, Yu
    Xu, Jiangnan
    Niu, Yanyan
    Bromberg, Jonathan S.
    Ding, Yaozhong
    JOURNAL OF IMMUNOLOGY, 2008, 181 (12): : 8700 - 8710
  • [27] The lineage-defining factors T-bet and Bcl-6 collaborate to regulate Th1 gene expression patterns
    Oestreich, Kenneth J.
    Huang, Albert C.
    Weinmann, Amy S.
    JOURNAL OF EXPERIMENTAL MEDICINE, 2011, 208 (05): : 1001 - 1013
  • [28] T-Bet Enhances Regulatory T Cell Fitness and Directs Control of Th1 Responses in Crescentic GN
    Nosko, Anna
    Kluger, Malte A.
    Diefenhardt, Paul
    Melderis, Simon
    Wegscheid, Claudia
    Tiegs, Gisa
    Stahl, Rolf A. K.
    Panzer, Ulf
    Steinmetz, Oliver M.
    JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2017, 28 (01): : 185 - 196
  • [29] T-Bet Deficient Mice Are Protected from Helicobacter Induced Mucosal Injury: Role of T-Bet in the Induction of Inflammatory Cytokines
    Stoicov, Calin
    Liu, Jian Hua
    Cerny, Anna
    Bowen, Glennice
    Kurt-Jones, Evelyn A.
    Houghton, Jean Marie
    GASTROENTEROLOGY, 2009, 136 (05) : A42 - A42
  • [30] HIV-1 Tat modulates T-bet expression and induces Th1 type of immune response
    Kulkarni, A
    Ravi, DS
    Singh, K
    Rampalli, S
    Parekh, V
    Mitra, D
    Chattopadhyay, S
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 329 (02) : 706 - 712