Radzioch D, Varesio L
McGill University, Montreal General Hospital Research Institute, Quebec, Canada.
Mol Cell Biol. 1991 May;11(5):2718-22. doi: 10.1128/mcb.11.5.2718-2722.1991.
Treatment of macrophages with interferon-gamma (IFN gamma) strongly decreased the induction of c-fos mRNA by 12-O-tetradecanoylphorbol-13-acetate (TPA), lipopolysaccharide, or calcium ionophore A23187 in macrophages. Under the same experimental conditions, IFN gamma induced oligo(A) synthetase mRNA and did not affect the constitutive expression of transforming growth factor beta mRNA, indicating that IFN gamma did not induce general degradation of mRNAs. Run-on experiments indicated that c-fos was constitutively transcribed at low levels and that TPA augmented c-fos transcription. IFN gamma did not inhibit constitutive or TPA-induced c-fos transcription. However, IFN gamma decreased c-fos mRNA stability, as assessed by measuring the half-life of c-fos mRNA in actinomycin D-treated cells. These results indicated that IFN gamma inhibited c-fos mRNA induction by TPA at the posttranscriptional level.
用γ干扰素(IFNγ)处理巨噬细胞,可显著降低12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)、脂多糖或钙离子载体A23187在巨噬细胞中诱导c - fos mRNA的表达。在相同实验条件下,IFNγ可诱导寡聚(A)合成酶mRNA的表达,且不影响转化生长因子β mRNA的组成型表达,这表明IFNγ不会诱导mRNA的普遍降解。连续转录实验表明,c - fos以低水平持续转录,TPA可增强c - fos的转录。IFNγ不会抑制c - fos的组成型转录或TPA诱导的转录。然而,通过测量放线菌素D处理细胞中c - fos mRNA的半衰期评估,IFNγ可降低c - fos mRNA的稳定性。这些结果表明,IFNγ在转录后水平抑制TPA诱导的c - fos mRNA表达。