NKT cells derive from double-positive thymocytes that are positively selected by CDId

被引:327
作者
Gapin, L
Matsuda, JL
Surh, CD
Kronenberg, M
机构
[1] La Jolla Inst Allergy & Immunol, San Diego, CA 92121 USA
[2] Univ Calif San Diego, Dept Biol, La Jolla, CA 92093 USA
[3] IMM26 Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.1038/ni710
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CDId-reactive NKT cells are a separate T cell sublineage. Instructive models propose that NKT cells branch off the mainstream developmental pathway because of their T cell antigen receptor specificity, whereas stochastic models would propose that they develop from precursor cells committed to this sublineage before variable-gene rearrangement. We show here that immature double-positive (DP) thymocytes form the canonical rearranged V-alpha gene of NKT cells at nearly equivalent frequencies in the presence or absence of CDId expression. After interacting with CDId in the thymus, these cells give rise to expanded populations of NKT cells - including both CD4(+) and double-negative lymphocytes in the thymus and periphery - that express this alpha chain. These results confirm the existence of a DP intermediate for CDId-reactive NKT cells. They also show that the early developmental stages of these T cells are not governed by a distinct mechanism, which is consistent with the TCR-instructive model of differentiation.
引用
收藏
页码:971 / 978
页数:8
相关论文
共 74 条
  • [1] Positive and negative selection invoke distinct signaling pathways
    AlberolaIla, J
    Hogquist, KA
    Swan, KA
    Bevan, MJ
    Perlmutter, RM
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (01) : 9 - 18
  • [2] Thymocyte selection: not by TCR alone
    Amsen, D
    Kruisbeek, AM
    [J]. IMMUNOLOGICAL REVIEWS, 1998, 165 : 209 - 229
  • [3] Murine natural killer cells contribute to the granulomatous reaction caused by mycobacterial cell walls
    Apostolou, I
    Takahama, Y
    Belmant, C
    Kawano, T
    Huerre, M
    Marchal, G
    Cui, J
    Taniguchi, M
    Nakauchi, H
    Fournié, JJ
    Kourilsky, P
    Gachelin, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) : 5141 - 5146
  • [4] AN NK1.1+ CD4+8- SINGLE-POSITIVE THYMOCYTE SUBPOPULATION THAT EXPRESSES A HIGHLY SKEWED T-CELL ANTIGEN RECEPTOR-V-BETA FAMILY
    ARASE, H
    ARASE, N
    OGASAWARA, K
    GOOD, RA
    ONOE, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) : 6506 - 6510
  • [5] NK1.1+ CD4+ CD8- THYMOCYTES WITH SPECIFIC LYMPHOKINE SECRETION
    ARASE, H
    ARASE, N
    NAKAGAWA, K
    GOOD, RA
    ONOE, K
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (01) : 307 - 310
  • [6] SELECTION IS NOT REQUIRED TO PRODUCE INVARIANT T-CELL RECEPTOR GAMMA-GENE JUNCTIONAL SEQUENCES
    ASARNOW, DM
    CADO, D
    RAULET, DH
    [J]. NATURE, 1993, 362 (6416) : 158 - 160
  • [7] Baldwin KK, 1999, J IMMUNOL, V163, P689
  • [8] Behar SM, 1999, J IMMUNOL, V162, P161
  • [9] ACTIVATION EVENTS DURING THYMIC SELECTION
    BENDELAC, A
    MATZINGER, P
    SEDER, RA
    PAUL, WE
    SCHWARTZ, RH
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (03) : 731 - 742
  • [10] Mouse CD1-specific NK1 T cells: Development, specificity, and function
    Bendelac, A
    Rivera, MN
    Park, SH
    Roark, JH
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 535 - 562