The c-kit(+) maturation pathway in mouse thymic T cell development: Lineages and selection

被引:53
作者
Akashi, K
Weissman, IL
机构
[1] STANFORD UNIV,SCH MED,DEPT DEV BIOL,STANFORD,CA 94305
[2] KYUSHU UNIV,FAC MED,DEPT INTERNAL MED 1,FUKUOKA 812,JAPAN
关键词
D O I
10.1016/S1074-7613(00)80491-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Positive selection of T cells begins with TCR alpha beta(lo) thymic progenitors. Here, we show that the most efficient TCR(lo) progenitors are c-kit(+) with intermediate levels of CD4 and CD8 (DPint). Positive selection of DPint TCR(lo) c-kit(+) cells results in TCR(med) CD69(+) c-kit(+) transitional intermediates that show increased TCRV beta frequencies to selecting superantigen (SAg) that are committed to the CD4 or CD8 pathway. The cells on the c-kit(+) maturation pathway maintain Bcl-2 expression. Most DPint c-kit(+) progenitors fail positive selection, and become DPhi c-kit(+) cells that lose Bcl-2 expression. Some DPhi c-kit blast cells can be salvaged to produce mature single-positive (SP) cells. DPint c-kit(+) maturation to SP cells can occur in <12 hr in vitro on thymic stromal monolayers.
引用
收藏
页码:147 / 161
页数:15
相关论文
共 79 条
  • [1] EARLY EVENTS IN T-CELL MATURATION
    ADKINS, B
    MUELLER, C
    OKADA, CY
    REICHERT, RA
    WEISSMAN, IL
    SPANGRUDE, GJ
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1987, 5 : 325 - 365
  • [2] ALAM SM, 1995, IMMUNITY, V3, P449
  • [3] INFLUENCE OF THE MAJOR HISTOCOMPATIBILITY COMPLEX ON POSITIVE THYMIC SELECTION OF V-BETA-17A+ T-CELLS
    BLACKMAN, MA
    MARRACK, P
    KAPPLER, J
    [J]. SCIENCE, 1989, 244 (4901) : 214 - 217
  • [4] DEVELOPMENT OF THE CD4 AND CD8 LINEAGE OF T-CELLS - INSTRUCTION VERSUS SELECTION
    BORGULYA, P
    KISHI, H
    MULLER, U
    KIRBERG, J
    VONBOEHMER, H
    [J]. EMBO JOURNAL, 1991, 10 (04) : 913 - 918
  • [5] REGULATION OF RAG-1 AND CD69 EXPRESSION IN THE THYMUS DURING POSITIVE AND NEGATIVE SELECTION
    BRANDLE, D
    MULLER, S
    MULLER, C
    HENGARTNER, H
    PIRCHER, H
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (01) : 145 - 151
  • [6] ANOTHER VIEW OF THE SELECTIVE MODEL OF THYMOCYTE SELECTION
    CHAN, SH
    COSGROVE, D
    WALTZINGER, C
    BENOIST, C
    MATHIS, D
    [J]. CELL, 1993, 73 (02) : 225 - 236
  • [7] DIFFERENTIATION POTENTIAL OF SUBSETS OF CD4-8- THYMOCYTES
    CRISPE, IN
    MOORE, MW
    HUSMANN, LA
    SMITH, L
    BEVAN, MJ
    SHIMONKEVITZ, RP
    [J]. NATURE, 1987, 329 (6137) : 336 - 339
  • [8] THYMOCYTE DEVELOPMENT IN MAJOR HISTOCOMPATIBILITY COMPLEX-DEFICIENT MICE - EVIDENCE FOR STOCHASTIC COMMITMENT TO THE CD4 AND CD8 LINEAGES
    CRUMP, AL
    GRUSBY, MJ
    GLIMCHER, LH
    CANTOR, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) : 10739 - 10743
  • [9] PIM-1 LEVELS DETERMINE THE SIZE OF EARLY B-LYMPHOID COMPARTMENTS IN BONE-MARROW
    DOMEN, J
    VANDERLUGT, NMT
    ACTON, D
    LAIRD, PW
    LINDERS, K
    BERNS, A
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (05) : 1665 - 1673
  • [10] 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