Transgenic expression of numb inhibits notch signaling in immature thymocytes but does not alter T cell fate specification

J Immunol. 2002 Apr 1;168(7):3173-80. doi: 10.4049/jimmunol.168.7.3173.

Abstract

The conserved adaptor protein Numb is an intrinsic cell fate determinant that functions by antagonizing Notch-mediated signal transduction. The Notch family of membrane receptors controls cell survival and cell fate determination in a variety of organ systems and species. Recent studies have identified a role for mammalian Notch-1 signals at multiple stages of T lymphocyte development. We have examined the role of mammalian Numb (mNumb) as a Notch regulator and cell fate determinant during T cell development. Transgenic overexpression of mNumb under the control of the Lck proximal promoter reduced expression of several Notch-1 target genes, indicating that mNumb antagonizes Notch-1 signaling in vivo. However, thymocyte development, cell cycle, and survival were unperturbed by mNumb overexpression, even though transgenic Numb was expressed at an early stage in thymocyte development (CD4(-)CD8(-)CD3(-) cells that were CD44(+)CD25(+) or CD44(-)CD25(+); double-negative 2/3). Moreover, bone marrow from mNumb transgenic mice showed no defects in thymopoiesis in competitive repopulation experiments. Our results suggest that mNumb functions as a Notch-1 antagonist in immature thymocytes, but that suppression of Notch-1 signaling at this stage does not alter gammadelta/alphabeta or CD4/CD8 T cell fate specification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / immunology
  • Cell Differentiation / immunology
  • Cell Survival / immunology
  • Drosophila / genetics
  • Drosophila Proteins
  • Gene Expression Regulation / immunology*
  • Humans
  • Immunophenotyping
  • Juvenile Hormones / biosynthesis*
  • Juvenile Hormones / genetics*
  • Juvenile Hormones / physiology
  • Lymph Nodes / cytology
  • Lymph Nodes / metabolism
  • Lymphocyte Count
  • Membrane Proteins / antagonists & inhibitors*
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Precipitin Tests
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • Protein Isoforms / physiology
  • Rats
  • Receptors, Notch
  • Signal Transduction / immunology*
  • Spleen / cytology
  • Spleen / metabolism
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / metabolism*
  • Thymus Gland / cytology
  • Thymus Gland / metabolism

Substances

  • Drosophila Proteins
  • Juvenile Hormones
  • Membrane Proteins
  • N protein, Drosophila
  • Protein Isoforms
  • Receptors, Notch
  • numb protein, Drosophila