Notch1 regulates maturation of CD4+ and CD8+ thymocytes by modulating TCR signal strength

Immunity. 2001 Mar;14(3):253-64. doi: 10.1016/s1074-7613(01)00107-8.

Abstract

Notch signaling regulates cell fate decisions in multiple lineages. We demonstrate in this report that retroviral expression of activated Notch1 in mouse thymocytes abrogates differentiation of immature CD4+CD8+ thymocytes into both CD4 and CD8 mature single-positive T cells. The ability of Notch1 to inhibit T cell development was observed in vitro and in vivo with both normal and TCR transgenic thymocytes. Notch1-mediated developmental arrest was dose dependent and was associated with impaired thymocyte responses to TCR stimulation. Notch1 also inhibited TCR-mediated signaling in Jurkat T cells. These data indicate that constitutively active Notch1 abrogates CD4+ and CD8+ maturation by interfering with TCR signal strength and provide an explanation for the physiological regulation of Notch expression during thymocyte development.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD / metabolism
  • Antigens, Differentiation, T-Lymphocyte / metabolism
  • CD4-Positive T-Lymphocytes / cytology*
  • CD4-Positive T-Lymphocytes / immunology
  • CD5 Antigens / metabolism
  • CD8-Positive T-Lymphocytes / cytology*
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Differentiation*
  • DNA-Binding Proteins / metabolism
  • Flow Cytometry
  • Gene Expression Regulation
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / metabolism
  • Humans
  • Jurkat Cells
  • Lectins, C-Type
  • Liver / cytology
  • Liver / embryology
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Transgenic
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Promoter Regions, Genetic / genetics
  • Receptor, Notch1
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Antigen, T-Cell / metabolism*
  • Receptors, Cell Surface*
  • Response Elements / genetics
  • Signal Transduction
  • Thymus Gland / cytology
  • Thymus Gland / immunology
  • Thymus Gland / metabolism
  • Transcription Factor AP-1 / metabolism
  • Transcription Factors / metabolism

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD5 Antigens
  • CD69 antigen
  • DNA-Binding Proteins
  • Histocompatibility Antigens Class I
  • Histocompatibility Antigens Class II
  • Lectins, C-Type
  • Membrane Proteins
  • NFATC Transcription Factors
  • NOTCH1 protein, human
  • Notch1 protein, mouse
  • Nuclear Proteins
  • Receptor, Notch1
  • Receptors, Antigen, T-Cell
  • Receptors, Cell Surface
  • Transcription Factor AP-1
  • Transcription Factors