Callewaert D M, Moudgil V K, Radcliff G, Waite R
Department of Chemistry, Oakland University, Rochester, MI 48309.
FEBS Lett. 1991 Jul 8;285(1):108-10. doi: 10.1016/0014-5793(91)80736-m.
Corticosteroids have previously been reported to partially inhibit the natural cytotoxic activity of peripheral blood lymphocytes. However, since only a few percent of peripheral lymphocytes are natural killer (NK) cells, it has not been possible to determine whether corticosteroids directly inhibit NK cells or mediate this effect via other cell types. This report documents direct functional inactivation, but unimpeded proliferation, of cloned human NK cells by subphysiologic levels of cortisol. In contrast, high concentrations of testosterone, progesterone or estradiol had no significant effect on proliferation or cytotoxic activity of the cloned NK cells. The kinetics of inhibition of NK function by cortisol are consistent with a transcription-dependent mechanism.
以前有报道称皮质类固醇可部分抑制外周血淋巴细胞的自然细胞毒性活性。然而,由于外周淋巴细胞中只有百分之几是自然杀伤(NK)细胞,因此无法确定皮质类固醇是直接抑制NK细胞还是通过其他细胞类型介导这种效应。本报告记录了亚生理水平的皮质醇可直接使克隆的人NK细胞功能失活,但不影响其增殖。相比之下,高浓度的睾酮、孕酮或雌二醇对克隆的NK细胞的增殖或细胞毒性活性没有显著影响。皮质醇抑制NK功能的动力学与转录依赖性机制一致。