Peng Bi-Wen, Lin Jian-yin, Zhang Tao
Medical College of Wuhan University, Wuhan, Hubei Province 430071, People's Republic of China.
Parasitol Res. 2008 Apr;102(5):1043-50. doi: 10.1007/s00436-007-0873-4. Epub 2008 Feb 28.
In this study, the intracellular signaling pathway of PGE2 synthesis in macrophages (RAW264.7) induced by Toxoplasma gondii was investigated. The T. gondii-induced PGE2 production in macrophages increased in a time-dependent manner, as PGE2 induction began at 4 h, peaked at 12 h, and then plateaued at a high level. COX-2 mRNA in macrophages was detectable as early as 4 h after treatment; the maximal expression was observed at 8 h. The earliest induction of COX-2 protein occurred at 4 h and peaked at 16 h; meanwhile, COX-1 mRNA level and protein production remained unchanged throughout. Indomethacin and nimesulide inhibited tachyzoite-induced PGE2 production and COX-2 mRNA expression in macrophages but they had no significant effect on COX-2 protein expression. EGTA, TFP and BAPTA/AM inhibited both arachidonic acid (AA) and PGE2 production without effecting COX-2 protein expression, but verapamil inhibited neither AA nor PGE2 production. H7 was found to inhibit PGE2 production, and COX-2 mRNA expression and protein expression by tachyzoite or LPS stimulated macrophages in a dose-dependent manner. Our results demonstrate that T. gondii induces PGE2 biosynthesis in RAW264.7 macrophages by regulating AA production through a calcium-dependent pathway and induction of COX-2 expression by a PKC-dependent pathway.
在本研究中,对弓形虫诱导的巨噬细胞(RAW264.7)中PGE2合成的细胞内信号通路进行了研究。弓形虫诱导的巨噬细胞中PGE2的产生呈时间依赖性增加,因为PGE2的诱导在4小时开始,12小时达到峰值,然后在高水平保持稳定。巨噬细胞中的COX-2 mRNA在处理后4小时即可检测到;在8小时观察到最大表达。COX-2蛋白最早在4小时诱导,16小时达到峰值;与此同时,COX-1 mRNA水平和蛋白产生在整个过程中保持不变。吲哚美辛和尼美舒利抑制速殖子诱导的巨噬细胞中PGE2的产生和COX-2 mRNA表达,但它们对COX-2蛋白表达没有显著影响。EGTA、TFP和BAPTA/AM抑制花生四烯酸(AA)和PGE2的产生,而不影响COX-2蛋白表达,但维拉帕米对AA和PGE2的产生均无抑制作用。发现H7以剂量依赖性方式抑制速殖子或LPS刺激的巨噬细胞中PGE2的产生、COX-2 mRNA表达和蛋白表达。我们的结果表明,弓形虫通过钙依赖性途径调节AA的产生,并通过PKC依赖性途径诱导COX-2表达,从而在RAW264.7巨噬细胞中诱导PGE2生物合成。