Nakajima Kazuyuki, Matsushita Yuichi, Tohyama Yoko, Kohsaka Shinichi, Kurihara Tadashi
Department of Bioinformatics, Faculty of Engineering, Soka University, Hachioji, Tokyo 192-8577, Japan.
Neurosci Lett. 2006 Jul 3;401(3):199-202. doi: 10.1016/j.neulet.2006.03.014. Epub 2006 Mar 31.
The molecular mechanism by which the deleterious cytokines interleukin 1 beta (IL-1beta) and tumor necrosis factor alpha (TNFalpha) are induced in endotoxin-stimulated microglia was investigated from the viewpoint of signal transduction. Neither cytokine is produced in nonstimulated rat microglia, but both are remarkably induced by stimulation with endotoxin lipopolysaccharide (LPS). LPS-inducible IL-1beta was significantly suppressed by pretreatment with the nuclear factor kappa B (NFkappaB) inhibitor ammonium pyrrolidine dithiocarbamate (APDC), but TNFalpha was not. APDC was actually confirmed to suppress the degradation of IkappaBalpha and IkappaBbeta in microglia, indicating a role for the inhibitor of NFkappaB activation. Taken together, these results suggest that the induction of IL-1beta and TNFalpha in endotoxin-stimulated microglia is differentially regulated at the level of NFkappaB activation.
从信号转导的角度研究了在内毒素刺激的小胶质细胞中诱导产生有害细胞因子白细胞介素1β(IL-1β)和肿瘤坏死因子α(TNFα)的分子机制。在未受刺激的大鼠小胶质细胞中这两种细胞因子均不产生,但在内毒素脂多糖(LPS)刺激下均显著诱导产生。用核因子κB(NFκB)抑制剂吡咯烷二硫代氨基甲酸铵(APDC)预处理可显著抑制LPS诱导的IL-1β产生,但对TNFα无此作用。实际上已证实APDC可抑制小胶质细胞中IκBα和IκBβ的降解,表明其在NFκB激活抑制剂方面的作用。综上所述,这些结果提示在内毒素刺激的小胶质细胞中IL-1β和TNFα的诱导在NFκB激活水平上受到不同调节。