| Literature DB >> 18776904 |
Lie Wang1, Kathryn F Wildt, Jinfang Zhu, Xianyu Zhang, Lionel Feigenbaum, Lino Tessarollo, William E Paul, B J Fowlkes, Rémy Bosselut.
Abstract
The transcription factors GATA-3 and ThPOK are required for intrathymic differentiation of CD4(+) T cells, but their precise functions in this process remain unclear. Here we show that, contrary to previous findings, Gata3 disruption blocked differentiation into the CD4(+) T cell lineage before commitment to the CD4(+) lineage and in some contexts permitted the 'redirection' of major histocompatibility complex class II-restricted thymocytes into the CD8(+) lineage. GATA-3 promoted ThPOK expression and bound to a region of the locus encoding ThPOK established as being critical for ThPOK expression. Finally, ThPOK promoted differentiation into the CD4(+) lineage in a way dependent on GATA-3 but inhibited differentiation into the CD8(+) lineage independently of GATA-3. We propose that GATA-3 acts as a specification factor for the CD4(+) lineage 'upstream' of the ThPOK-controlled CD4(+) commitment checkpoint.Entities:
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Year: 2008 PMID: 18776904 PMCID: PMC2805063 DOI: 10.1038/ni.1647
Source DB: PubMed Journal: Nat Immunol ISSN: 1529-2908 Impact factor: 25.606