Treatment of astroglial cells with interleukin 1 beta and interferon gamma transcriptionally activates the nitric oxide synthase (NOS)-2 gene. The duration of mRNA expression is brief because of transcript instability. In addition, NO donors reduce the expression of NOS-2 mRNA dramatically by reducing the rate of transcription. In this study we observed that the NO donor, spermine NONOate did not inhibit the activation and translocation of NF-kappa B, a key transcription factor in the induction of NOS-2, but inhibited formation of the NF-kappa B-DNA complex. This effect was reversed by methaemoglobin (acting as an NO trap) and by the reducing agent dithiothreitol. Formation of the interferon-regulatory factor-DNA complex was unaffected by NO. These results suggest that NO can modulate its own production by interfering with NF-kappa B interaction with the promoter region of the NOS gene, a negative feedback effect that may be important for limiting NO production in vivo.
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Park S. K., 1995, Society for Neuroscience Abstracts, V21, P1080