Kim Jong-Eun, Heo Yong-Seok, Lee Ki Won
Research Institute of Biotechnology and Medical Converged Science, Dongguk University-Seoul, Goyang, Republic of Korea.
WCU Biomodulation Major, Department of Agricultural Biotechnology and Center for Food and Bioconvergence, Seoul National University, Seoul, Republic of Korea.
J Cell Biochem. 2017 Nov;118(11):4080-4087. doi: 10.1002/jcb.26063. Epub 2017 May 23.
Solar ultraviolet light (sUV) has been shown to promote the development of skin disorders including inflammation, photoaging, and skin carcinogenesis. Osajin is the major bioactive isoflavone present in the fruit of Maclura pomifera, commonly referred to as the Osage orange. In this study, we observed that osajin inhibited sUV-induced cyclooxygenase (COX)-2 protein expression in both HaCaT and JB6 cells. COX-2 is a major mediator of skin inflammation. sUV activated the transcription factors nuclear factor-κB and activator protein-1 which, in turn, induces COX-2 expression. Osajin inhibited transactivation of these transcription factors. We identified RSK2 as an inhibitory target of osajin by screening against 68 kinases related to inflammation. Osajin binds with RSK2 directly in an ATP-competitive manner. Computer modeling simulated a plausible binding orientation between osajin and RSK2. Osajin inhibited sUV-induced phosphorylation of histone H3, a substrate of RSK2. However, sUV-induced phosphorylation of extracellular signal-regulated kinases, p38 kinase, c-Jun N-terminal kinase and Akt, which are signaling factors upstream of RSK2, was unchanged in the presence of osajin. The anti-inflammatory effects and molecular mechanism of osajin suggest that it may have utility as a functional food for skin health and cosmetic ingredient. J. Cell. Biochem. 118: 4080-4087, 2017. © 2017 Wiley Periodicals, Inc.
太阳紫外线(sUV)已被证明会促进包括炎症、光老化和皮肤癌发生在内的皮肤疾病的发展。奥沙金是桑橙果实中主要的生物活性异黄酮,桑橙通常被称为奥塞奇橙。在本研究中,我们观察到奥沙金在HaCaT和JB6细胞中均抑制sUV诱导的环氧化酶(COX)-2蛋白表达。COX-2是皮肤炎症的主要介质。sUV激活转录因子核因子-κB和活化蛋白-1,进而诱导COX-2表达。奥沙金抑制这些转录因子的反式激活。通过针对68种与炎症相关的激酶进行筛选,我们确定RSK2是奥沙金的抑制靶点。奥沙金以ATP竞争方式直接与RSK2结合。计算机建模模拟了奥沙金与RSK2之间可能的结合方向。奥沙金抑制sUV诱导的组蛋白H3磷酸化,组蛋白H3是RSK2的底物。然而,在存在奥沙金的情况下,sUV诱导的细胞外信号调节激酶、p38激酶、c-Jun氨基末端激酶和Akt的磷酸化(这些是RSK2上游的信号因子)没有变化。奥沙金的抗炎作用和分子机制表明,它可能作为一种有益于皮肤健康的功能性食品和化妆品成分。《细胞生物化学杂志》118: 4080 - 4087, 2017。© 2017威利期刊公司