| Literature DB >> 20802152 |
Takeshi Yamada1, Kirsten Gierach, Ping-Hsien Lee, Xiaohong Wang, H Daniel Lacorazza.
Abstract
T cell receptor activation inhibits expression of the E74-like factor (ELF) 4 and Krüppel-like factor 4 genes to release naive CD8(+) T cells from their quiescent state. In this study, we show that ELF4 controls the ERK-mediated proliferative response by maintaining normal levels of dual-specificity phosphatases 1 and 5 in CD8(+) T cells. In activated CD8(+) T cells, the mammalian target of rapamycin pathway inhibits ELF4 and Krüppel-like factor 4 expression downstream of ERK and PI3K signaling. Our findings demonstrate that rapamycin could be used to modulate expression of this transcriptional network involved in cell-cycle regulation.Entities:
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Year: 2010 PMID: 20802152 PMCID: PMC2943983 DOI: 10.4049/jimmunol.1000718
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422