| Literature DB >> 22425249 |
Mary Elizabeth Jones-Mason1, Xudong Zhao, Dietmar Kappes, Anna Lasorella, Antonio Iavarone, Yuan Zhuang.
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. Copyright ÂEntities:
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Year: 2012 PMID: 22425249 PMCID: PMC3431168 DOI: 10.1016/j.immuni.2012.02.010
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745