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甲萘醌(维生素K3)通过激活Mel-Ab细胞中的ERK来减少黑色素合成。

Menadione (Vitamin K3) decreases melanin synthesis through ERK activation in Mel-Ab cells.

作者信息

Kim Eun-Hyun, Kim Myo-Kyoung, Yun Hye-Young, Baek Kwang Jin, Kwon Nyoun Soo, Park Kyoung-Chan, Kim Dong-Seok

机构信息

Department of Biochemistry, Chung-Ang University College of Medicine, 221 Heukseok-dong, Dongjak-gu, Seoul 156-756, Korea.

出版信息

Eur J Pharmacol. 2013 Oct 15;718(1-3):299-304. doi: 10.1016/j.ejphar.2013.08.018. Epub 2013 Sep 3.

Abstract

Menadione is a synthetic vitamin K3 derivative. Here, we examined the effects of menadione on melanogenesis and its related signaling pathways. Our results showed that melanin content was significantly reduced after menadione treatment in a dose-dependent manner. However, menadione treatment did not reduce tyrosinase activity directly. Wnt signaling is known to play a major role in the control of melanin synthesis. Thus, we tested the effects of menadione treatment on GSK3β and β-catenin signaling, but found that menadione did not influence either of these signaling pathways. We also investigated changes in the phosphorylation of ERK, which is related to melanin regulation. These results indicated that menadione treatment led to the phosphorylation of ERK. Additionally, menadione treatment reduced both MITF and tyrosinase protein levels. Treatment with PD98059, a specific ERK pathway inhibitor, restored menadione-induced melanin reduction and also prevented MITF and tyrosinase downregulation by menadione. These results suggest that the hypopigmentary action of menadione is due to MITF and tyrosinase downregulation by ERK activation.

摘要

甲萘醌是一种合成的维生素K3衍生物。在此,我们研究了甲萘醌对黑色素生成及其相关信号通路的影响。我们的结果表明,甲萘醌处理后黑色素含量以剂量依赖性方式显著降低。然而,甲萘醌处理并未直接降低酪氨酸酶活性。已知Wnt信号在黑色素合成的控制中起主要作用。因此,我们测试了甲萘醌处理对GSK3β和β-连环蛋白信号的影响,但发现甲萘醌对这两种信号通路均无影响。我们还研究了与黑色素调节相关的ERK磷酸化的变化。这些结果表明,甲萘醌处理导致ERK磷酸化。此外,甲萘醌处理降低了MITF和酪氨酸酶蛋白水平。用特异性ERK通路抑制剂PD98059处理可恢复甲萘醌诱导的黑色素减少,并防止甲萘醌导致的MITF和酪氨酸酶下调。这些结果表明,甲萘醌的色素减退作用是由于ERK激活导致MITF和酪氨酸酶下调。

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