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IL-27 and IFN-alpha signal via Stat1 and Stat3 and induce T-Bet and IL-12Rbeta2 in naive T cells.
Hibbert, Linda; Pflanz, Stefan; De Waal Malefyt, Rene; Kastelein, Robert A.
Afiliação
  • Hibbert L; Department of Discovery Biology, DNAX Research Institute, Palo Alto, CA 94304, USA.
J Interferon Cytokine Res ; 23(9): 513-22, 2003 Sep.
Article em En | MEDLINE | ID: mdl-14565860
ABSTRACT
Interleukin-27 (IL-27) supports proliferation of naive CD4(+) T cells and enhances interferon-gamma (IFN-gamma) production by activated T cells and natural killer (NK) cells. We report here that IL-27 induces Stat1 and Stat3 phosphorylation and activation in human and murine cell lines and primary human T cells. IL-27 also induces T-Bet, a Stat1-dependent gene crucial to Th1 cell commitment. Similarly, IFN-alpha activates Stat1 and Stat3 and T-Bet expression in naive T cells. Induction of T-Bet results in upregulation of IL-12Rbeta2 on naive T cells, which is essential for responsiveness to IL-12 and differentiation to a Th1 phenotype. Both IL-27 and IFN-alpha induce expression of IL-12Rbeta2 in T cells. In contrast, IFN-gamma, which activates Stat1 but not Stat3, induces expression of T-Bet but not IL-12Rbeta2 in naive T cells. We propose that IL-27 and IFN-alpha are important for early Th1 commitment and act upstream of IL-12 and IFN-gamma in this pathway.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Linfócitos T / Interleucinas / Interferon-alfa / Receptores de Interleucina Limite: Humans Idioma: En Revista: J Interferon Cytokine Res Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Estados Unidos
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Linfócitos T / Interleucinas / Interferon-alfa / Receptores de Interleucina Limite: Humans Idioma: En Revista: J Interferon Cytokine Res Assunto da revista: ALERGIA E IMUNOLOGIA Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Estados Unidos