An Sang Mi, Koh Jae-Sook, Boo Yong Chool
Department of Molecular Medicine and Cell and Matrix Research Institute, BK21 Medical Education Program for Human Resources, Kyungpook National University School of Medicine, Daegu, Korea.
BMB Rep. 2009 Mar 31;42(3):178-83. doi: 10.5483/bmbrep.2009.42.3.178.
Tyrosinase (TYR) plays a critical role in cellular melanogenesis and, thus, has been the major target of pharmacological approaches for the control of skin pigmentation. This study examined an alternative molecular approach using TYR-small interfering RNA (siRNA) to control melanogenesis in the human melanocytes. Both the mRNA and protein levels of TYR were significantly lowered by TYR-siRNA treatment, whereas TYR-related protein 1 and TYR-related protein 2 displayed no such changes. TYR-siRNA treatment inhibited the cellular melanin synthesis from the externally supplied TYR substrate L-tyrosine. TYR-siRNA also suppressed melanin synthesis and decreased the viability of cells exposed to ultraviolet radiation, supporting a critical role of melanin in protection against ultraviolet radiation. These results suggest that molecular approaches using siRNA targeted to the enzymes of melanogenic pathway may provide a novel strategy for the control of cell pigmentation.
酪氨酸酶(TYR)在细胞黑色素生成过程中起着关键作用,因此一直是控制皮肤色素沉着的药理学方法的主要靶点。本研究探讨了一种使用TYR小干扰RNA(siRNA)来控制人黑素细胞中黑色素生成的替代分子方法。通过TYR-siRNA处理,TYR的mRNA和蛋白质水平均显著降低,而TYR相关蛋白1和TYR相关蛋白2则无此变化。TYR-siRNA处理抑制了从外部提供的TYR底物L-酪氨酸合成细胞黑色素。TYR-siRNA还抑制了黑色素合成,并降低了暴露于紫外线辐射的细胞的活力,这支持了黑色素在抵御紫外线辐射中的关键作用。这些结果表明,针对黑色素生成途径中酶的siRNA分子方法可能为控制细胞色素沉着提供一种新策略。