Burres N S, Premachandran U, Hoselton S, Cwik D, Hochlowski J E, Ye Q, Sunga G N, Karwowski J P, Jackson M, Whittern D N
Abbott Laboratories, Abbott Park, Illinois 60064, USA.
J Antibiot (Tokyo). 1995 May;48(5):380-6. doi: 10.7164/antibiotics.48.380.
Determination of the mechanism of action of FK506 and cyclosporin A has yielded new molecular targets involved in signal transduction during T cell activation. A common target of FK506 and cyclosporin A is inhibition of activation of the NFAT transcription factor, for which a specific binding region is present in the promoter of the IL-2 gene. A reporter gene assay has been used to screen for agents that interfere with this early step in T cell activation. Simple aromatic compounds that block NFAT-dependent transcription and show in vitro immunosuppressive activity were isolated from the broth and mycelia of two Streptomyces sp. fermentations. The compounds were active at concentrations that were not directly cytotoxic.
对FK506和环孢菌素A作用机制的研究揭示了T细胞激活过程中涉及信号转导的新分子靶点。FK506和环孢菌素A的一个共同靶点是抑制NFAT转录因子的激活,IL-2基因启动子中存在该转录因子的特异性结合区域。已使用报告基因检测法筛选干扰T细胞激活这一早期步骤的药物。从两种链霉菌发酵的肉汤和菌丝体中分离出了能阻断NFAT依赖性转录并具有体外免疫抑制活性的简单芳香族化合物。这些化合物在不具有直接细胞毒性的浓度下具有活性。