E Protein Transcription Factors Are Required for the Development of CD4 + Lineage T Cells

Mary Elizabeth Jones-Mason, Xudong Zhao, Dietmar Kappes, Anna Lasorella, Antonio Iavarone, Yuan Zhuang

Research output: Contribution to journalArticlepeer-review

79 Scopus citations

Abstract

The double-positive (DP) to single-positive (SP) transition during T cell development is initiated by downregulation of the E protein transcription factors HEB and E2A. Here, we have demonstrated that in addition to regulating the onset of this transition, HEB and E2A also play a separate role in CD4 + lineage choice. Deletion of HEB and E2A in DP thymocytes specifically blocked the development of CD4 + lineage T cells. Furthermore, deletion of the E protein inhibitors Id2 and Id3 allowed CD4 + T cell development but blocked CD8 + lineage development. Analysis of the CD4 + lineage transcriptional regulators ThPOK and Gata3 placed HEB and E2A upstream of CD4 + lineage specification. These studies identify an important role for E proteins in the activation of CD4 + lineage differentiation as thymocytes undergo the DP to SP transition.

Original languageEnglish
Pages (from-to)348-361
Number of pages14
JournalImmunity
Volume36
Issue number3
DOIs
StatePublished - Mar 23 2012

Keywords

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors/deficiency
  • CD4 Antigens/genetics
  • CD4-Positive T-Lymphocytes/cytology
  • CD8-Positive T-Lymphocytes/cytology
  • Cell Differentiation/immunology
  • Inhibitor of Differentiation Protein 2/deficiency
  • Inhibitor of Differentiation Proteins/deficiency
  • Interleukin-7 Receptor alpha Subunit/metabolism
  • Mice
  • Mice, 129 Strain
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Receptors, CCR7/metabolism
  • Up-Regulation

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