Laboratory Animal Center, College of Animal Sciences, Jilin University, Xi'an Road, 5333#, Jilin, 130062, China.
Lipids Health Dis. 2018 Feb 9;17(1):26. doi: 10.1186/s12944-018-0673-0.
Arachidonic acid (AA) has potent pro-apoptotic effects on cancer cells at a low concentration and on macrophages at a very high concentration. However, the effects of AA on the macrophage cell cycle and related signaling pathways have not been fully investigated. Herein we aim to observe the effect of AA on macrophages cell cycle.
AA exposure reduced the viability and number of macrophages in a dose- and time-dependent manner. The reduction in RAW264.7 cell viability was not caused by apoptosis, as indicated by caspase-3 and activated caspase-3 detection. Further research illustrated that AA exposure induced RAW264.7 cell cycle arrested at S phase, and some cell cycle-regulated proteins were altered accordingly. Moreover, JNK signaling was stimulated by AA, and the stimulation was partially reversed by a JNK signaling inhibitor in accordance with cell cycle-related factors. In addition, nuclear and total Foxo1/3a and phosphorylated Foxo1/3a were elevated by AA in a dose- and time-dependent manner, and this elevation was suppressed by the JNK signaling inhibitor.
Our study demonstrated that AA inhibits macrophage viability by inducing S phase cell cycle arrest. The JNK signaling pathway and the downstream FoxO transcription factors are involved in AA-induced RAW264.7 cell cycle arrest.
花生四烯酸(AA)在低浓度时对癌细胞具有强烈的促凋亡作用,在极高浓度时对巨噬细胞具有强烈的促凋亡作用。然而,AA 对巨噬细胞细胞周期及相关信号通路的影响尚未得到充分研究。在此,我们旨在观察 AA 对巨噬细胞细胞周期的影响。
AA 暴露以剂量和时间依赖的方式降低巨噬细胞的活力和数量。Caspase-3 和活化的 caspase-3 检测表明,RAW264.7 细胞活力的降低不是由细胞凋亡引起的。进一步的研究表明,AA 暴露诱导 RAW264.7 细胞周期停滞在 S 期,相应地改变了一些细胞周期调节蛋白。此外,AA 刺激 JNK 信号通路,而 JNK 信号通路抑制剂部分逆转了与细胞周期相关的因子。此外,AA 以剂量和时间依赖的方式上调核和总 Foxo1/3a 及磷酸化 Foxo1/3a,而 JNK 信号通路抑制剂抑制了这种上调。
我们的研究表明,AA 通过诱导 S 期细胞周期阻滞抑制巨噬细胞活力。JNK 信号通路和下游的 FoxO 转录因子参与了 AA 诱导的 RAW264.7 细胞周期阻滞。