Menu

Javascript is not activated in your browser. This website needs javascript activated to work properly.
You are here

Inhibition of EBF function by active Notch signaling reveals a novel regulatory pathway in early B-cell development

Author:
  • Emma Smith
  • P Akerblad
  • T Kadesch
  • Håkan Axelson
  • Mikael Sigvardsson
Publishing year: 2005
Language: English
Pages: 1995-2001
Publication/Series: Blood
Volume: 106
Issue: 6
Document type: Journal article
Publisher: American Society of Hematology

Abstract english

The Notch signaling pathway is involved in several lineage commitment and differentiation events. One of these is fate determination of the common lymphoid progenitor, promoting T-cell development at the expense of B-cell differentiation. It has been suggested that this process relies on Notch's ability to inhibit E proteins, which are crucial for early B-cell development. Here, we report that Notch signaling also modulates the function of the transcription factor, early B-cell factor (EBF). Transient transfection of intracellular Notch1 (Notch1-IC) into a pre-B cell line resulted in the down-regulation of EBF-regulated promoters and diminished the capacity of EBF to activate these promoters in an epithelial cell line. This correlated with a reduction in the ability of EBF to bind DNA. Ligand-induced stimulation of endogenous Notch receptors with Delta4 mimicked the activity of Notch1-IC toward EBF. These data suggest that Notch signaling may affect B- versus T-lineage commitment by the targeting of both EBF and E2A.

Keywords

  • Hematology

Other

Published
  • ISSN: 1528-0020
Håkan Axelson
E-mail: hakan.axelson [at] med.lu.se

Professor

Division of Translational Cancer Research

+46 46 222 64 34

MV 404 A31A2

90