Olivera D L, Kaplan J M, Newman-Tarr T, Ruggieri E V, Badger A M
Department of Cellular Biochemistry, SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania 19406-0939.
Clin Immunol Immunopathol. 1993 Sep;68(3):357-62. doi: 10.1006/clin.1993.1138.
The immunosuppressive effects of cyclosporin A, FK506, and rapamycin were compared in mouse and rat systems of in vitro cellular stimulation. The inhibitory profile of rapamycin was distinctly different in the two species. In mouse systems, rapamycin caused a dose-dependent inhibition of both Ca(2+)-dependent (concanavalin A (Con A), phytohemagglutinin (PHA), and phorbol 12-myristate 13-acetate + ionomycin) and Ca(2+)-independent (lipopolysaccharide and PMA + interleukin-2) activation, whereas in the rat only Ca(2+)-independent responses were inhibited. Rapamycin's lack of activity in Ca(2+)-dependent responses in the rat does not appear to reside in a general insensitivity of this pathway to inhibition as cyclosporin A and FK506 demonstrated potent inhibitory activity. Additionally, rapamycin was able to block the inhibitory effect of FK506 on rat cells stimulated with the Ca(2+)-dependent stimulus, Con A. These results indicate a further dissociation in the biological activity of rapamycin compared to cyclosporin A and FK506 and may point to intriguing species differences in the immunosuppressive effects of these compounds in vitro.
在小鼠和大鼠的体外细胞刺激系统中比较了环孢素A、FK506和雷帕霉素的免疫抑制作用。雷帕霉素的抑制模式在这两个物种中明显不同。在小鼠系统中,雷帕霉素对钙依赖性(刀豆球蛋白A(Con A)、植物血凝素(PHA)以及佛波醇12-肉豆蔻酸酯13-乙酸酯+离子霉素)和钙非依赖性(脂多糖和PMA+白细胞介素-2)激活均产生剂量依赖性抑制,而在大鼠中仅钙非依赖性反应受到抑制。雷帕霉素在大鼠钙依赖性反应中缺乏活性,这似乎并非源于该途径对抑制普遍不敏感,因为环孢素A和FK506显示出强大的抑制活性。此外,雷帕霉素能够阻断FK506对用钙依赖性刺激物Con A刺激的大鼠细胞的抑制作用。这些结果表明,与环孢素A和FK506相比,雷帕霉素的生物活性进一步解离,这可能表明这些化合物在体外免疫抑制作用中存在有趣的物种差异。