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未能表达TCRβ和/或TCRγδ蛋白的未成熟胸腺细胞在CD44(-)CD25(-)(DN4)亚群中通过凋亡性细胞死亡而死亡。

Immature thymocytes that fail to express TCRbeta and/or TCRgamma delta proteins die by apoptotic cell death in the CD44(-)CD25(-) (DN4) subset.

作者信息

Falk I, Nerz G, Haidl I, Krotkova A, Eichmann K

机构信息

Max-Planck-Institut für Immunbiologie, Freiburg, Germany.

出版信息

Eur J Immunol. 2001 Nov;31(11):3308-17. doi: 10.1002/1521-4141(200111)31:11<3308::aid-immu3308>3.0.co;2-5.

DOI:10.1002/1521-4141(200111)31:11<3308::aid-immu3308>3.0.co;2-5
PMID:11745348
Abstract

Pre-TCR/CD3 signals are essential for survival and maturation of (CD44(-)25(+)) DN3 thymocytes via the (CD44(-)25(-)) DN4 stage to CD4(+)CD8(+) (DP) cells, a process termed beta-selection. The exact developmental stages of apoptosis resulting from lack of pre-TCR/CD3 signals have so far not been determined. Here we analyzed apoptotic cell death in relation to expression of clonotypic TCR polypeptides and to cell cycle status in immature thymocyte subpopulations of wild type (wt) mice and of several strains of mice with compromised pre-TCR/CD3 signaling complexes. In wt mice or pre-TCR/CD3-deficient mice, apoptotic cells could not be detected among DN3 cells but accumulated in a subset of DN4 expressing CD69. Apoptotic CD69(+)DN4 cells were rare in wt mice and were found among DN4 cells that were negative or low for intracellular TCRbeta and negative for TCRgamma delta polypeptide chains. Apoptotic CD69(+)DN4 cells were abundant in pre-TCR/CD3 signaling-deficient mice in which most DN4 cells failed to express clonotypic TCR polypeptides. Survival of DN4 cells, but not maturation of DN3 cells to DN4, was found to depend on the expression of clonotypic TCR polypeptides in the same cell. The results suggest that thymocytes unsuccessful in alpha beta or in gamma delta lineage development die by apoptosis in the DN4 subset.

摘要

前T细胞受体/CD3信号对于(CD44(-)25(+))双阴性3(DN3)胸腺细胞通过(CD44(-)25(-))双阴性4(DN4)阶段存活并成熟为CD4(+)CD8(+)(双阳性,DP)细胞至关重要,这一过程称为β选择。迄今为止,因缺乏前T细胞受体/CD3信号而导致的凋亡的确切发育阶段尚未确定。在此,我们分析了野生型(wt)小鼠以及几种前T细胞受体/CD3信号复合物受损的小鼠品系的未成熟胸腺细胞亚群中,凋亡细胞死亡与克隆型T细胞受体多肽表达以及细胞周期状态的关系。在wt小鼠或前T细胞受体/CD3缺陷小鼠中,在DN3细胞中未检测到凋亡细胞,但在表达CD69的DN4亚群中积累。凋亡的CD69(+)DN4细胞在wt小鼠中很少见,且存在于细胞内TCRβ呈阴性或低表达以及TCRγδ多肽链呈阴性的DN4细胞中。在大多数DN4细胞未能表达克隆型T细胞受体多肽的前T细胞受体/CD3信号缺陷小鼠中,凋亡的CD69(+)DN4细胞大量存在。发现DN4细胞的存活而非DN3细胞向DN4细胞的成熟取决于同一细胞中克隆型T细胞受体多肽的表达。结果表明,在αβ或γδ谱系发育中不成功的胸腺细胞在DN4亚群中通过凋亡死亡。

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