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 language | English |
|---|---|
| Pages (from-to) | 348-361 |
| Number of pages | 14 |
| Journal | Immunity |
| Volume | 36 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 23 2012 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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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