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

Ingrid Falk, Gabi Nerz, Ian Haidl, Anna Krotkova, Klaus Eichmann

Research output: Contribution to journalArticlepeer-review

34 Citations (Scopus)

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 β-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 TCRβ and negative for TCRγδ 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 αβ or in γδ lineage development die by apoptosis in the DN4 subset.

Original languageEnglish
Pages (from-to)3308-3317
Number of pages10
JournalEuropean Journal of Immunology
Volume31
Issue number11
DOIs
Publication statusPublished - 2001
Externally publishedYes

ASJC Scopus Subject Areas

  • Immunology and Allergy
  • Immunology

PubMed: MeSH publication types

  • Journal Article

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