Successive expression and activation of NFAT family members during thymocyte differentiation

被引:36
作者
Adachi, S
Amasaki, Y
Miyatake, S
Arai, N
Iwata, M
机构
[1] Mitsubishi Kasei Inst Life Sci, Integrat Projects, Tokyo 1948511, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Mol & Dev Biol, CREST,Minato Ku, Tokyo 1080071, Japan
[3] DNAX Res Inst Mol & Cellular Biol Inc, Dept Immunol, Palo Alto, CA 94304 USA
关键词
D O I
10.1074/jbc.275.19.14708
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
Differentiation of immature CD4(+)CD8(+) thymocytes to mature CD4(+) or CD8(+) T cells is induced by positive selection and appears to involve calcineurin-dependent activation of NFAT, a family of transcription factors. NFATx is predominantly expressed in CD4(+)CD8(+) thymocytes, whereas NFATp and NFATc are expressed at much lower levels in the thymus than in mature T cells. However, how or when each NFAT member is involved in the differentiation pathway is unclear. Using an in vitro model system where isolated CD4(+)CD8(+) thymocytes can survive and differentiate into semi-mature CD4-lineage T cells, we suggest that low calcineurin activity sustained for approximately 20 h is required for cell survival and differentiation. Accordingly, the DNA binding activity of NFAT slowly increased during the stimulation of 20 h to induce the differentiation. NFATx significantly contributed to the early rise, but the late increase was mostly due to NFATc activation. Meanwhile, the expression of NFATx mRNA decreased and that of NFATc mRNA increased. The DNA-binding activity of NFATp was detectable but low throughout the stimulation. NFATp became dominantly active after the semi-mature T cells differentiated into mature and activated CD4 T cells. These findings suggest that NFATx and NFATc successively play roles in T cell development.
引用
收藏
页码:14708 / 14716
页数:9
相关论文
共 65 条
  • [1] SELECTIVE REQUIREMENT FOR MAP KINASE ACTIVATION IN THYMOCYTE DIFFERENTIATION
    ALBEROLAILA, J
    FORBUSH, KA
    SEGER, R
    KREBS, EG
    PERLMUTTER, RM
    [J]. NATURE, 1995, 373 (6515) : 620 - 623
  • [2] Amasaki Y, 1998, J IMMUNOL, V160, P2324
  • [3] T cell antigen receptor signal transduction pathways
    Cantrell, D
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 : 259 - 274
  • [4] Specific regulation of Fos family transcription factors in thymocytes at two developmental checkpoints
    Chen, F
    Chen, D
    Rothenberg, EV
    [J]. INTERNATIONAL IMMUNOLOGY, 1999, 11 (05) : 677 - 688
  • [5] Surface molecules that drive T cell development in vitro in the absence of thymic epithelium and in the absence of lineage-specific signals
    Cibotti, R
    Punt, JA
    Dash, KS
    Sharrow, SO
    Singer, A
    [J]. IMMUNITY, 1997, 6 (03) : 245 - 255
  • [6] CALCIUM SIGNALING
    CLAPHAM, DE
    [J]. CELL, 1995, 80 (02) : 259 - 268
  • [7] DEUSCH K, 1990, J IMMUNOL, V144, P2851
  • [8] Differential activation of transcription factors induced by Ca2+ response amplitude and duration
    Dolmetsch, RE
    Lewis, RS
    Goodnow, CC
    Healy, JI
    [J]. NATURE, 1997, 386 (6627) : 855 - 858
  • [9] KINETICS OF MATURE T-CELL DEVELOPMENT IN THE THYMUS
    EGERTON, M
    SCOLLAY, R
    SHORTMAN, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) : 2579 - 2582
  • [10] FINE JS, 1991, J IMMUNOL, V147, P2852