The Ets Transcription Factor ERM Is Th1-Specific and Induced by IL-12 Through a Stat4-Dependent Pathway

Interleukin 12 (IL-12)-induced T helper 1 (Th1) development requires Stat4 activation. However, antigen-activated Th1 cells can produce interferon γ (IFN-γ) independently of IL-12 and Stat4 activation. Thus, in differentiated Th1 cells, factors regulated by IL-12 and Stat4 may be involved in IFN-γ p...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1999-03, Vol.96 (7), p.3888-3893
Hauptverfasser: Ouyang, Wenjun, Jacobson, Nils G., Bhattacharya, Deepta, Gorham, James D., Fenoglio, Domenic, Sha, William C., Murphy, Theresa L., Murphy, Kenneth M.
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Sprache:eng
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Zusammenfassung:Interleukin 12 (IL-12)-induced T helper 1 (Th1) development requires Stat4 activation. However, antigen-activated Th1 cells can produce interferon γ (IFN-γ) independently of IL-12 and Stat4 activation. Thus, in differentiated Th1 cells, factors regulated by IL-12 and Stat4 may be involved in IFN-γ production. Using subtractive cloning, we identified ERM, an Ets transcription factor, to be a Th1-specific, IL-12-induced gene. IL-12-induction of ERM occurred in wild-type and Stat1-deficient, but not Stat4-deficient, T cells, suggesting ERM is Stat4-inducible. Retroviral expression of ERM did not restore IFN-γ production in Stat4-deficient T cells, but augmented IFN-γ expression in Stat4-heterozygous T cells. Ets factors frequently regulate transcription via cooperative interactions with other transcription factors, and ERM has been reported to cooperate with c-Jun. However, in the absence of other transcription factors, ERM augmented expression of an IFN-γ reporter by only 2-fold. Thus, determining the requirement for ERM in Th1 development likely will require gene targeting.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.96.7.3888