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Hirseins inhibit melanogenesis by regulating the gene expressions of Mitf and melanogenesis enzymes.

机译:赫尔辛菌素通过调节Mitf和黑色素生成酶的基因表达来抑制黑色素生成。

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Previously, we reported that Thymelaea hirsuta extract has antimelanogenesis effect on B16 murine melanoma cells. The extract was subjected to fractionation, and hirsein A (HA) and hirsein B (HB) were discovered and tested for their ability to regulate melanogenesis in B16 cells. Western blot (WB) analysis was carried out to determine the expression of tyrosinase. Moreover, to elucidate the possible mechanism behind melanogenesis regulation, real-time PCR using primers for Mitf, Tyr, Trp1 and Dct genes, and protein kinase C (PKC) activity assay were carried out. Results clearly show that 0.1 mum HA and HB significantly reduced the melanin content. This reduction in melanin content was accompanied by reduced tyrosinase expression as detected by WB analysis. There was also a significant decrease in the expression level of Mitf gene in HA- and HB-treated cells. HA down-regulated the expressions of Tyr, Trp1 and Dct, whereas HB down-regulated only those of Trp1 and Dct. Interestingly, HB-treated cells had lower kinase activity than HA-treated cells indicating a possible difference in the activities of the compounds but with the same mechanism of melanogenesis regulation. We report for the first time that HA and HB can down-regulate melanogenesis by down-regulating Mitf gene expression, leading to reduced expressions of Tyr, Trp1 and Dct. The hirseins were also able to reduce the kinase activity, suggesting the possible involvement of PKC in the overall ability of the hirseins to down-regulate melanogenesis.
机译:以前,我们报道了Th草胸腺提取物对B16鼠黑色素瘤细胞具有促白细胞生成作用。对提取物进行分级分离,发现了hirsein A(HA)和hirsein B(HB)并测试了它们调节B16细胞黑素生成的能力。进行蛋白质印迹(WB)分析以确定酪氨酸酶的表达。此外,为阐明黑素生成调控的可能机制,进行了使用Mitf,Tyr,Trp1和Dct基因引物的实时PCR以及蛋白激酶C(PKC)活性测定。结果清楚地表明,0.1 m的HA和HB可以显着降低黑色素含量。黑色素含量的降低伴随着酪氨酸酶表达的降低,如通过WB分析所检测到的。在HA和HB处理的细胞中,Mitf基因的表达水平也显着降低。 HA下调Tyr,Trp1和Dct的表达,而HB仅下调Trp1和Dct的表达。有趣的是,HB处理的细胞比HA处理的细胞具有更低的激酶活性,这表明化合物的活性可能存在差异,但具有相同的黑色素生成调节机制。我们首次报道HA和HB可以通过下调Mitf基因表达来下调黑色素生成,从而导致Tyr,Trp1和Dct的表达降低。 hirseins还能够降低激酶活性,表明PKC可能参与了hirseins下调黑色素生成的整体能力。

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