Literature DB >> 7510419

Requirement for transcription factor IRF-1 in NO synthase induction in macrophages.

R Kamijo1, H Harada, T Matsuyama, M Bosland, J Gerecitano, D Shapiro, J Le, S I Koh, T Kimura, S J Green.   

Abstract

Production of nitric oxide (NO) by macrophages is important for the killing of intracellular infectious agents. Interferon (IFN)-gamma and lipopolysaccharide stimulate NO production by transcriptionally up-regulating the inducible NO synthase (iNOS). Macrophages from mice with a targeted disruption of the IFN regulatory factor-1 (IRF-1) gene (IRF-1-/- mice) produced little or no NO and synthesized barely detectable iNOS messenger RNA in response to stimulation. Two adjacent IRF-1 response elements were identified in the iNOS promoter. Infection with Mycobacterium bovis (BCG) was more severe in IRF-1-/- mice than in wild-type mice. Thus, IRF-1 is essential for iNOS activation in murine macrophages.

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Year:  1994        PMID: 7510419     DOI: 10.1126/science.7510419

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  197 in total

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5.  Altered immune response of interferon regulatory factor 1-deficient mice against Plasmodium berghei blood-stage malaria infection.

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Review 7.  Regulation of T helper cell differentiation by interferon regulatory factor family members.

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9.  Induction of iNOS expression and antimicrobial activity by interferon (IFN)-beta is distinct from IFN-gamma in Burkholderia pseudomallei-infected mouse macrophages.

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10.  Nitric oxide suppression of human hematopoiesis in vitro. Contribution to inhibitory action of interferon-gamma and tumor necrosis factor-alpha.

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Journal:  J Clin Invest       Date:  1995-08       Impact factor: 14.808

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