STAT5 is required for thymopoiesis in a development stage-specific manner

被引:40
作者
Kang, JS
DiBenedetto, B
Narayan, K
Zhao, H
Der, SD
Chambers, CA
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Grad Program Immunol & Virol, Worcester, MA 01655 USA
[2] Univ Toronto, Dept Lab Med & Pathol, Program Proteom & Bioinformat, Toronto, ON, Canada
关键词
D O I
10.4049/jimmunol.173.4.2307
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Diverse cytokines necessary for normal lymphopoiesis and lymphocyte homeostasis activate STAT5 in responder cells. Although STAT5 has been suggested to be a central molecular effecter of IL-7 function, its essential role during IL-7-dependent T cell development in vivo remained unclear. Using Stat5(-/-) mice we now show that STAT5 is essential for various functions ascribed to IL-7 in vivo. STAT5 is required for embryonic thymocyte production, TCRgamma gene transcription, and Peyer's patch development. In sharp contrast, normal STAT5 is dispensable for adult thymopoiesis. In peripheral lymphocytes, STAT5 is primarily required for the generation and/or maintenance of gammadelta T cells and TCRgammadelta(+) intraepithelial lymphocytes. Collectively, these results demonstrate that STAT5 is critical for many, but not all, aspects of steady state lymphoid lineage development and maintenance and suggest the existence of previously undocumented cytokine signaling traits and/or cytokine milieu during adult thymopoiesis.
引用
收藏
页码:2307 / 2314
页数:8
相关论文
共 50 条
  • [1] Three distinctive steps in Peyer's patch formation of murine embryo
    Adachi, S
    Yoshida, H
    Kataoka, H
    Nishikawa, S
    [J]. INTERNATIONAL IMMUNOLOGY, 1997, 9 (04) : 507 - 514
  • [2] THE IMMUNOBIOLOGY OF T-CELLS WITH INVARIANT GAMMA-DELTA ANTIGEN RECEPTORS
    ALLISON, JP
    HAVRAN, WL
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 : 679 - 705
  • [3] A novel element upstream of the Vγ2 gene in the murine T cell receptor γ locus cooperates with the 3′ enhancer to act as a locus control region
    Baker, JE
    Kang, J
    Xiong, N
    Chen, T
    Cado, D
    Raulet, DH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (05) : 669 - 679
  • [4] Molecular determinants of TCR expression and selection
    Berg, LJ
    Kang, JS
    [J]. CURRENT OPINION IN IMMUNOLOGY, 2001, 13 (02) : 232 - 241
  • [5] Developmental changes in the differentiation capacity of haematopoietic stem cells
    Bonifer, C
    Faust, N
    Geiger, H
    Müller, AM
    [J]. IMMUNOLOGY TODAY, 1998, 19 (05): : 236 - 241
  • [6] Cell intrinsic defects in cytokine responsiveness of STAT5-deficient hematopoietic stem cells
    Bradley, HL
    Hawley, TS
    Bunting, KD
    [J]. BLOOD, 2002, 100 (12) : 3983 - 3989
  • [7] Reduced lymphomyeloid repopulating activity from adult bone marrow and fetal liver of mice lacking expression of STAT5
    Bunting, KD
    Bradley, HL
    Hawley, TS
    Moriggl, R
    Sorrentino, BP
    Ihle, JN
    [J]. BLOOD, 2002, 99 (02) : 479 - 487
  • [8] CTLA-4-mediated inhibition in regulation of T cell responses: Mechanisms and manipulation in tumor immunotherapy
    Chambers, CA
    Kuhns, MS
    Egen, JG
    Allison, JP
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 : 565 - 594
  • [9] Contractor NV, 1998, J IMMUNOL, V160, P385
  • [10] The interleukin-7 receptor alpha chain transmits distinct signals for proliferation and differentiation during B lymphopoiesis
    Corcoran, AE
    Smart, FM
    Cowling, RJ
    Crompton, T
    Owen, MJ
    Venkitaraman, AR
    [J]. EMBO JOURNAL, 1996, 15 (08) : 1924 - 1932