Department of Dermatology, Huashan Hospital, FuDan University, Shanghai, China.
Dermatology. 2012;224(2):145-53. doi: 10.1159/000336777. Epub 2012 May 3.
UVB light can generate potentially harmful hydrogen peroxide (H(2)O(2)) in vivo, but it can also promote the beneficial proliferation and migration of melanocytes. The successful use of UVB monotherapy for treatment of vitiligo suggests that H(2)O(2) may have a biphasic effect on melanin synthesis and melanosome transfer.
To study the beneficial role of H(2)O(2) on melanogenesis and melanosome transport in living melanocytes and keratinocytes.
A co-culture system model was constructed using the primary human melanocytes and keratinocytes. The MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay was used to determine cell proliferation, NaOH was used to determine the melanin content, and real-time PCR was used to determine tyrosinase expression. Western blot was used to determine Rab-27A and protease-activated receptor 2 (PAR-2) expression.
This study demonstrated that tyrosinase was activated by low concentrations of H(2)O(2) (≤0.3 mM); however, this activity was downregulated by high concentrations of H(2)O(2) (>0.3 mM). Activation of high levels of melanin synthesis was induced when cells were treated with low concentrations of H(2)O(2) (0.3 mM). Further observation using an in vitro co-culture system of fluorescein (carboxyfluorescein diacetate succinimidyl ester, CFDA-SE)-labeled melanocytes and keratinocytes indicated that melanosome transfer occurred in normal human epidermal melanocytes. Fluorescence microscopy revealed increased melanosome transfer into keratinocytes treated with 0.3 mM H(2)O(2) in the co-culture compared to the control. Examination of melanosomes in the keratinocytes by flow cytometry confirmed these results. Furthermore, treatment with H(2)O(2) (0.3 mM) upregulated the expression of Rab-27A and PAR-2, significant proteins involved in melanosome transfer, according to Western blot.
These results confirmed that low concentration levels of H(2)O(2) play a major role in the regulation of human pigmentation by increasing melanin synthesis and melanosome transfer.
UVB 光在体内可以产生潜在有害的过氧化氢(H2O2),但也可以促进黑素细胞的有益增殖和迁移。UVB 单一疗法成功用于治疗白癜风表明 H2O2 可能对黑色素合成和黑素小体转移有双相作用。
研究 H2O2 对活黑素细胞和角质形成细胞中黑色素生成和黑素小体转运的有益作用。
构建了原代人黑素细胞和角质形成细胞的共培养系统模型。MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴盐)测定法用于测定细胞增殖,NaOH 用于测定黑色素含量,实时 PCR 用于测定酪氨酸酶表达。Western blot 用于测定 Rab-27A 和蛋白酶激活受体 2(PAR-2)表达。
本研究表明,低浓度的 H2O2(≤0.3mM)激活酪氨酸酶;然而,高浓度的 H2O2(>0.3mM)则下调其活性。当用低浓度的 H2O2(0.3mM)处理细胞时,会诱导高水平的黑色素合成被激活。进一步使用体外共培养系统观察到用荧光素(羧基荧光素二乙酸琥珀酰亚胺酯,CFDA-SE)标记的黑素细胞和角质形成细胞,表明黑素小体转移发生在正常的人表皮黑素细胞中。荧光显微镜显示,与对照相比,共培养中用 0.3mM H2O2 处理的黑素细胞向角质形成细胞中转移的黑素小体增加。通过流式细胞术检查角质形成细胞中的黑素小体证实了这些结果。此外,Western blot 显示,用 H2O2(0.3mM)处理可上调 Rab-27A 和 PAR-2 的表达,Rab-27A 和 PAR-2 是参与黑素小体转移的重要蛋白质。
这些结果证实,低浓度的 H2O2 通过增加黑色素合成和黑素小体转移,在调节人类色素沉着中起主要作用。