Drira Riadh, Sakamoto Kazuichi
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.
Life Sci. 2015 Dec 15;143:43-9. doi: 10.1016/j.lfs.2015.10.009. Epub 2015 Oct 23.
The beneficial effects of 4'-O-methylated flavonoids on induction of melanogenesis are well established. Here, we report the effect of isosakuranetin (Iso) on melanogenesis in B16BL6 melanoma cells and an analysis of the signaling pathways involved in this activity.
B16BL6 melanoma cells were treated with several concentrations of Iso and melanin content was measured. Activation and expression of factors involved in melanogenesis were assessed via western blotting.
Iso (15 and 30μmol/L) strongly stimulated melanogenesis in a dose-dependent manner. Iso increased tyrosinase activity and up-regulated tyrosinase (Tyr), tyrosinase related protein 1 (TRP1), and tyrosinase related protein 2 (TRP2) in a time-dependent manner. Iso decreased B16 cell proliferation at a concentration above 45μmol/L, and had no effect on cell viability as revealed by MTT and trypan blue assays. Iso up-regulated expression of microphthalmia transcription factor (MITF), with a maximum effect after 12h. H89, a specific inhibitor of PKA, showed that MITF up-regulation is mediated through PKA/CREB activation. Furthermore, Iso decreased phosphorylation of MITF at Ser73 after 24h and 48h of exposure, activating MITF and leading to up-regulation of Tyr, TRP1, and TRP2. Iso inhibited phosphorylation and activation of ERK1/2 after 12h, while no significant effects on p38 and JNK phosphorylation were observed. Iso inhibited AKT phosphorylation and led to activation of GSK3β.
Iso stimulates melanogenesis in B16 melanoma cells via up-regulation of MITF. Furthermore, Iso-induced inhibition of ERK1/2 and PI3K/AKT signaling pathways activate MITF and subsequent expression of Tyr, TRP1, and TRP2.
4'-O-甲基化黄酮类化合物对黑色素生成的诱导作用已得到充分证实。在此,我们报告异樱花素(Iso)对B16BL6黑色素瘤细胞黑色素生成的影响,并分析参与该活性的信号通路。
用几种浓度的Iso处理B16BL6黑色素瘤细胞,并测量黑色素含量。通过蛋白质印迹法评估黑色素生成相关因子的激活和表达。
Iso(15和30μmol/L)以剂量依赖性方式强烈刺激黑色素生成。Iso以时间依赖性方式增加酪氨酸酶活性,并上调酪氨酸酶(Tyr)、酪氨酸酶相关蛋白1(TRP1)和酪氨酸酶相关蛋白2(TRP2)。Iso在浓度高于45μmol/L时降低B16细胞增殖,MTT和台盼蓝试验显示其对细胞活力无影响。Iso上调小眼畸形相关转录因子(MITF)的表达,在12小时后达到最大效应。PKA的特异性抑制剂H89表明,MITF的上调是通过PKA/CREB激活介导的。此外,Iso在暴露24小时和48小时后降低MITF在Ser73位点的磷酸化,激活MITF并导致Tyr、TRP1和TRP2的上调。Iso在12小时后抑制ERK1/2的磷酸化和激活,而对p38和JNK磷酸化未观察到显著影响。Iso抑制AKT磷酸化并导致GSK3β激活。
Iso通过上调MITF刺激B16黑色素瘤细胞中的黑色素生成。此外,Iso诱导的ERK1/2和PI3K/AKT信号通路的抑制激活了MITF以及随后Tyr、TRP1和TRP2的表达。