Stevenson M A, Zhao M J, Asea A, Coleman C N, Calderwood S K
Department of Adult Oncology, Joint Center for Radiation Therapy, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 1999 Nov 15;163(10):5608-16.
Sodium salicylate (NaSal) and other nonsteroidal anti-inflammatory drugs (NSAIDs) coordinately inhibit the activity of NF-kappa B, activate heat shock transcription factor 1 and suppress cytokine gene expression in activated monocytes and macrophages. Because our preliminary studies indicated that these effects could be mimicked by inhibitors of signal transduction, we have studied the effects of NSAIDs on signaling molecules potentially downstream of LPS receptors in activated macrophages. Our findings indicate that ribosomal S6 kinase 2 (RSK2), a 90-kDa ribosomal S6 kinase with a critical role as an effector of the RAS-mitogen-activated protein kinase pathway and a regulator of immediate early gene transcription is a target for inhibition by the NSAIDs. NSAIDs inhibited the activity of purified RSK2 kinase in vitro and of RSK2 in mammalian cells and suppressed the phosphorylation of RSK2 substrates cAMP response element binding protein (CREB) and I-kappa B alpha in vivo. Additionally, NaSal inhibited the phosphorylation by RSK2 of CREB and I-kappa B alpha on residues crucial for their transcriptional activity in vivo and thus repressed CREB and NF-kappa B-dependent transcription. These experiments suggest that RSK2 is a target for NSAIDs in the inhibition of monocyte-specific gene expression and indicate the importance of RSK2 and related kinases in cell regulation, indicating a new area for anti-inflammatory drug discovery.
水杨酸钠(NaSal)和其他非甾体抗炎药(NSAIDs)协同抑制核因子-κB(NF-κB)的活性,激活热休克转录因子1并抑制活化的单核细胞和巨噬细胞中细胞因子基因的表达。由于我们的初步研究表明这些效应可被信号转导抑制剂模拟,我们研究了NSAIDs对活化巨噬细胞中LPS受体潜在下游信号分子的影响。我们的研究结果表明,核糖体S6激酶2(RSK2),一种90 kDa的核糖体S6激酶,作为RAS-丝裂原活化蛋白激酶途径的效应器和即时早期基因转录的调节因子发挥关键作用,是NSAIDs的抑制靶点。NSAIDs在体外抑制纯化的RSK2激酶的活性以及在哺乳动物细胞中抑制RSK2的活性,并在体内抑制RSK2底物环磷酸腺苷反应元件结合蛋白(CREB)和I-κBα的磷酸化。此外,NaSal在体内抑制RSK2对CREB和I-κBα在其转录活性至关重要的残基上的磷酸化,从而抑制CREB和NF-κB依赖性转录。这些实验表明RSK2是NSAIDs抑制单核细胞特异性基因表达的靶点,并表明RSK2和相关激酶在细胞调节中的重要性,为抗炎药物发现指明了一个新领域。