Nakano T, Ohara O, Teraoka H, Arita H
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.
J Biol Chem. 1990 Jul 25;265(21):12745-8.
We investigated the effects of glucocorticoids on group II phospholipase A2 (PLA2) expression in rat cultured smooth muscle cells. Both forskolin-induced and tumor necrosis factor (TNF)-induced PLA2 release responses were almost completely blocked by 10 and 100 nM dexamethasone, respectively, as assayed by protein blotting and PLA2 activity assays. Dexamethasone-mediated inhibition of PLA2 release appeared to be mediated by the glucocorticoid receptor. Dexamethasone at concentrations greater than 10 nM inhibited forskolin-induced elevation of the group II PLA2 mRNA level but not TNF-induced elevation. These data suggest that the mechanism mediating forskolin-induced mRNA accumulation is sensitive to glucocorticoids, but the mechanism mediating the TNF-induced accumulation is not. Inhibition of TNF-induced PLA2 release by glucocorticoids may be explained by the blocking of post-transcriptional synthesis of the group II PLA2.
我们研究了糖皮质激素对大鼠培养平滑肌细胞中Ⅱ型磷脂酶A2(PLA2)表达的影响。通过蛋白质印迹法和PLA2活性测定法检测发现,10 nM和100 nM地塞米松分别几乎完全阻断了福斯高林诱导的和肿瘤坏死因子(TNF)诱导的PLA2释放反应。地塞米松介导的对PLA2释放的抑制作用似乎是由糖皮质激素受体介导的。浓度大于10 nM的地塞米松抑制了福斯高林诱导的Ⅱ型PLA2 mRNA水平的升高,但不抑制TNF诱导的升高。这些数据表明,介导福斯高林诱导的mRNA积累的机制对糖皮质激素敏感,但介导TNF诱导的积累的机制不敏感。糖皮质激素对TNF诱导的PLA2释放的抑制作用可能是由于阻断了Ⅱ型PLA2的转录后合成。