Kim Ji Hye, Lee Jae-Eun, Kim Taewon, Yeom Myung Hun, Park Jun Seong, di Luccio Eric, Chen Hanyong, Dong Zigang, Lee Ki Won, Kang Nam Joo
School of Food Science and Biotechnology, Kyungpook National University, Daegu, South Korea.
Korean Medicine Application Center, Korea Institute of Oriental Medicine, Daegu, South Korea.
Front Mol Biosci. 2020 Dec 3;7:577284. doi: 10.3389/fmolb.2020.577284. eCollection 2020.
7,3',4'-Trihydroxyisoflavone (7,3',4'-THIF) is a metabolite of daidzein which is a representative isoflavone found in soybean. Recent studies suggested that 7,3',4'-THIF exerts a hypopigmentary effect in B16F10 cells, however, its underlying molecular mechanisms and specific target protein remain unknown. Here, we found that 7,3',4'-THIF, but not daidzein, inhibited α-melanocyte-stimulating hormone (MSH)-induced intracellular and extracellular melanin production in B16F10 cells by directly targeting melanocortin 1 receptor (MC1R). Western blot data showed that 7,3',4'-THIF inhibited α-MSH-induced tyrosinase, tyrosinase-related protein-1 (TYRP-1), and tyrosinase-related protein-2 (TYRP-2) expressions through the inhibition of Microphthalmia-associated transcription factor (MITF) expression and cAMP response element-binding (CREB) phosphorylation. 7,3',4'-THIF also inhibited α-MSH-induced dephosphorylation of AKT and phosphorylation of p38 and cAMP-dependent protein kinase (PKA). cAMP and Pull-down assays indicated that 7,3',4'-THIF strongly inhibited forskolin-induced intracellular cAMP production and bound MC1R directly by competing with α-MSH. Moreover, 7,3',4'-THIF inhibited α-MSH-induced intracellular melanin production in human epidermal melanocytes (HEMs). Collectively, these results demonstrate that 7,3',4'-THIF targets MC1R, resulting in the suppression of melanin production, suggesting a protective role for 7,3',4'-THIF against melanogenesis.
7,3',4'-三羟基异黄酮(7,3',4'-THIF)是大豆苷元的一种代谢产物,大豆苷元是大豆中一种具有代表性的异黄酮。最近的研究表明,7,3',4'-THIF对B16F10细胞具有色素减退作用,然而,其潜在的分子机制和特定靶蛋白仍不清楚。在这里,我们发现7,3',4'-THIF而非大豆苷元,通过直接靶向促黑素细胞激素1受体(MC1R)抑制α-促黑素细胞激素(MSH)诱导的B16F10细胞内和细胞外黑色素生成。蛋白质印迹数据显示,7,3',4'-THIF通过抑制小眼畸形相关转录因子(MITF)表达和cAMP反应元件结合蛋白(CREB)磷酸化,抑制α-MSH诱导的酪氨酸酶、酪氨酸酶相关蛋白-1(TYRP-1)和酪氨酸酶相关蛋白-2(TYRP-2)表达。7,3',4'-THIF还抑制α-MSH诱导的AKT去磷酸化以及p38和cAMP依赖性蛋白激酶(PKA)的磷酸化。cAMP和下拉实验表明,7,3',4'-THIF强烈抑制福斯高林诱导的细胞内cAMP生成,并通过与α-MSH竞争直接结合MC1R。此外,7,3',4'-THIF抑制α-MSH诱导的人表皮黑素细胞(HEMs)内黑色素生成。总的来说,这些结果表明7,3',4'-THIF靶向MC1R,导致黑色素生成受到抑制,提示7,3',4'-THIF对黑色素生成具有保护作用。