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
  • [31] ISOLATION OF THE CYCLOSPORINE-SENSITIVE T-CELL TRANSCRIPTION FACTOR NFATP
    MCCAFFREY, PG
    LUO, C
    KERPPOLA, TK
    JAIN, J
    BADALIAN, TM
    HO, AM
    BURGEON, E
    LANE, WS
    LAMBERT, JN
    CURRAN, T
    VERDINE, GL
    RAO, A
    HOGAN, PG
    [J]. SCIENCE, 1993, 262 (5134) : 750 - 754
  • [32] IONOMYCIN ENHANCES CA2+ INFLUX BY STIMULATING STORE-REGULATED CATION ENTRY AND NOT BY A DIRECT ACTION AT THE PLASMA-MEMBRANE
    MORGAN, AJ
    JACOB, R
    [J]. BIOCHEMICAL JOURNAL, 1994, 300 : 665 - 672
  • [33] ESSENTIAL ROLE FOR ZAP-70 IN BOTH POSITIVE AND NEGATIVE SELECTION OF THYMOCYTES
    NEGISHI, I
    MOTOYAMA, N
    NAKAYAMA, K
    NAKAYAMA, K
    SENJU, S
    HATAKEYAMA, S
    ZHANG, Q
    CHAN, AC
    LOH, DY
    [J]. NATURE, 1995, 376 (6539) : 435 - 438
  • [34] NF-AT COMPONENTS DEFINE A FAMILY OF TRANSCRIPTION FACTORS TARGETED IN T-CELL ACTIVATION
    NORTHROP, JP
    HO, SN
    CHEN, L
    THOMAS, DJ
    TIMMERMAN, LA
    NOLAN, GP
    ADMON, A
    CRABTREE, GR
    [J]. NATURE, 1994, 369 (6480) : 497 - 502
  • [35] In vitro differentiation and commitment of CD4+CD8+ thymocytes to the CD4 lineage without TCR engagement
    Ohoka, Y
    Kuwata, T
    Tozawa, Y
    Zhao, Y
    Mukai, M
    Motegi, Y
    Suzuki, R
    Yokoyama, M
    Iwata, M
    [J]. INTERNATIONAL IMMUNOLOGY, 1996, 8 (03) : 297 - 306
  • [36] Ohoka Y, 1997, J IMMUNOL, V158, P5707
  • [37] The transcription factor NFAT4 is involved in the generation and survival of T cells
    Oukka, M
    Ho, IC
    de la Brousse, FC
    Hoey, T
    Grusby, MJ
    Glimcher, LH
    [J]. IMMUNITY, 1998, 9 (03) : 295 - 304
  • [38] Molecular cloning and functional characterization of murine cDNA encoding transcription factor NFATc
    Pan, S
    KoyanoNakagawa, N
    Tsuruta, L
    Amasaki, Y
    Yokota, T
    Mori, S
    Arai, N
    Arai, K
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (02) : 314 - 323
  • [39] Porritt HE, 1998, EUR J IMMUNOL, V28, P1197, DOI 10.1002/(SICI)1521-4141(199804)28:04<1197::AID-IMMU1197>3.0.CO
  • [40] 2-N