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刺橙素通过增加小眼畸形相关转录因子和酪氨酸酶的表达诱导黑色素生成的作用。

Melanogenesis-inducing effect of cirsimaritin through increases in microphthalmia-associated transcription factor and tyrosinase expression.

作者信息

Kim Hyo Jung, Kim Il Soon, Dong Yin, Lee Ik-Soo, Kim Jin Sook, Kim Jong-Sang, Woo Je-Tae, Cha Byung-Yoon

机构信息

Research Institute for Biological Functions, Chubu University, 1200 Matsumoto, Kasugai, Aichi 487-8501, Japan.

KM Convergence Research Division, Korea Institute of Oriental Medicine, Daejeon 305-811, Korea.

出版信息

Int J Mol Sci. 2015 Apr 20;16(4):8772-88. doi: 10.3390/ijms16048772.

DOI:10.3390/ijms16048772
PMID:25903150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4425108/
Abstract

The melanin-inducing properties of cirsimaritin were investigated in murine B16F10 cells. Cirsimaritin is an active flavone with methoxy groups, which is isolated from the branches of Lithocarpus dealbatus. Tyrosinase activity and melanin content in murine B16F10 melanoma cells were increased by cirsimaritin in a dose-dependent manner. Western blot analysis revealed that tyrosinase, tyrosinase-related protein (TRP) 1, TRP2 protein levels were enhanced after treatment with cirsimaritin for 48 h. Cirsimaritin also upregulated the expression of microphthalmia-associated transcription factor (MITF) after 24 h of treatment. Furthermore, cirsimaritin induced phosphorylation of cyclic adenosine monophosphate (cAMP) response element-binding protein (CREB) in a dose-dependent manner after treatment for 15 min. The cirsimaritin-mediated increase of tyrosinase activity was significantly attenuated by H89, a cAMP-dependent protein kinase A inhibitor. These findings indicate that cirsimaritin stimulates melanogenesis in B16F10 cells by activation of CREB as well as upregulation of MITF and tyrosinase expression, which was activated by cAMP signaling. Finally, the melanogenic effect of cirsimaritin was confirmed in human epidermal melanocytes. These results support the putative application of cirsimaritin in ultraviolet photoprotection and hair coloration treatments.

摘要

在小鼠B16F10细胞中研究了 cirsimaritin 的黑色素诱导特性。Cirsimaritin 是一种具有甲氧基的活性黄酮,从白皮柯的树枝中分离得到。Cirsimaritin 以剂量依赖的方式增加了小鼠B16F10黑色素瘤细胞中的酪氨酸酶活性和黑色素含量。蛋白质免疫印迹分析显示,用cirsimaritin处理48小时后,酪氨酸酶、酪氨酸酶相关蛋白(TRP)1、TRP2的蛋白水平增强。处理24小时后,Cirsimaritin还上调了小眼畸形相关转录因子(MITF)的表达。此外,处理15分钟后,cirsimaritin以剂量依赖的方式诱导环磷酸腺苷(cAMP)反应元件结合蛋白(CREB)的磷酸化。cAMP依赖性蛋白激酶A抑制剂H89显著减弱了cirsimaritin介导的酪氨酸酶活性增加。这些发现表明,cirsimaritin通过激活CREB以及上调由cAMP信号激活的MITF和酪氨酸酶表达来刺激B16F10细胞中的黑色素生成。最后,在人表皮黑素细胞中证实了cirsimaritin的黑色素生成作用。这些结果支持了cirsimaritin在紫外线光保护和染发治疗中的假定应用。

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