The biology of Stat4 and Stat6

被引:248
作者
Wurster, AL
Tanaka, T
Grusby, MJ
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
关键词
Stat4; Stat6; T helper cells;
D O I
10.1038/sj.onc.1203485
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
regulators of the proliferation, differentiation and functional capacity of lymphocytes, STATs (signal transducers and activators of transcription) are transcription factors that provide a direct link between the cytokine receptors and cytokine induced gene transcription. Stat6 and Stat4 are two STAT family members that specifically mediate signals that emanate from the IL-4 and IL-12 receptors, respectively, Recently a great deal of progress has been made in understanding the specific roles that Stat6 and Stat4 play in lymphocyte function through in vitro as well as in vivo studies using Stat6 and Stat4-deficient mice. This report will summarize and describe the recent advances made in understanding the activation and regulation of Stat6 and Stat4 as well as their roles in the development of an immune response.
引用
收藏
页码:2577 / 2584
页数:8
相关论文
共 103 条
  • [91] Multistage regulation of Th1-type immune responses by the transcription factor IRF-1
    Taki, S
    Sato, T
    Ogasawara, K
    Fukuda, T
    Sato, M
    Hida, S
    Suzuki, G
    Mitsuyama, M
    Shin, EH
    Kojima, S
    Taniguchi, T
    Asano, Y
    [J]. IMMUNITY, 1997, 6 (06) : 673 - 679
  • [92] Requirement for Stat4 in interleukin-12-mediated responses of natural killer and T cells
    Thierfelder, WE
    vanDeursen, JM
    Yamamoto, K
    Tripp, RA
    Sarawar, SR
    Carson, RT
    Sangster, MY
    Vignali, DAA
    Doherty, PC
    Grosveld, GC
    Ihle, JN
    [J]. NATURE, 1996, 382 (6587) : 171 - 174
  • [93] Venkataraman C, 1999, J IMMUNOL, V162, P4053
  • [94] Structure of the amino-terminal protein interaction domain of STAT-4
    Vinkemeier, U
    Moarefi, I
    Darnell, JE
    Kuriyan, J
    [J]. SCIENCE, 1998, 279 (5353) : 1048 - 1052
  • [95] Wang KS, 1999, J IMMUNOL, V162, P299
  • [96] MAXIMAL ACTIVATION OF TRANSCRIPTION BY STAT1 AND STAT3 REQUIRES BOTH TYROSINE AND SERINE PHOSPHORYLATION
    WEN, ZL
    ZHONG, Z
    DARNELL, JE
    [J]. CELL, 1995, 82 (02) : 241 - 250
  • [97] Wu CY, 1997, J IMMUNOL, V159, P1658
  • [98] Cooperative DNA binding and sequence-selective recognition conferred by the STAT amino-terminal domain
    Xu, XA
    Sun, YL
    Hoey, T
    [J]. SCIENCE, 1996, 273 (5276) : 794 - 797
  • [99] STAT4, A NOVEL GAMMA-INTERFERON ACTIVATION SITE-BINDING PROTEIN EXPRESSED IN EARLY MYELOID DIFFERENTIATION
    YAMAMOTO, K
    QUELLE, FW
    THIERFELDER, WE
    KREIDER, BL
    GILBERT, DJ
    JENKINS, NA
    COPELAND, NG
    SILVENNOINEN, O
    IHLE, JN
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (07) : 4342 - 4349
  • [100] The transcription factor GATA-3 is necessary and sufficient for Th2 cytokine gene expression in CD4 T cells
    Zheng, WP
    Flavell, RA
    [J]. CELL, 1997, 89 (04) : 587 - 596