中华皮肤科杂志 ›› 2015, Vol. 48 ›› Issue (10): 705-709.

• 论著 • 上一篇    下一篇

姜黄素对人表皮黑素细胞活性、迁移及c-kit mRNA表达量的影响

李其林,陆小娟,牛牧   

  1. 暨南大学第四附属医院,广州市红十字会医院皮肤科
  • 收稿日期:2015-01-26 修回日期:2015-05-26 发布日期:2015-09-28
  • 通讯作者: 李其林 E-mail:qlli_cn@163.com
  • 基金资助:

    广东省科技计划项目:姜黄素对人表皮黑色素细胞调控作用的研究

Effect of curcumin on the activity and migration of as well as c-kit mRNA expression in melanocytes

  • Received:2015-01-26 Revised:2015-05-26 Published:2015-09-28

摘要:

目的 探讨姜黄素对人表皮黑素细胞活性、黑素细胞迁移及c-kit mRNA相对表达量的影响。方法 不同浓度(5、10、20、30 μmol/L)姜黄素对人表皮黑素细胞活性影响实验,分为阴性对照组(添加MelM-2完全培养基 + 细胞)、药物对照组(MelM-2完全培养基 + 姜黄素)、空白对照组(仅添加MelM-2完全培养基)及实验组(MelM-2完全培养基 + 姜黄素 + 细胞),用MTS法分别检测培养24 h、48 h后细胞活性。划痕实验检测黑素细胞迁移的情况,实时荧光定量PCR检测黑素细胞c-kit mRNA相对表达量。实验分为对照组(仅添加MelM-2完全培养基 + 细胞)及3个浓度(5、10、20 μmol/L)实验组。 结果 不同浓度(5、10、20、30 μmol/L)姜黄素培养基培养黑素细胞24 h、48 h时,与对照组相比,30 μmol/L组均可明显抑制黑素细胞的增殖(P < 0.05),其他浓度差异无统计学意义(均P > 0.05)。划痕实验结果显示,与对照组相比,在培养48 h时,5、10、20 μmol/L姜黄素均能显著抑制黑素细胞迁移(均P < 0.05)。实时荧光定量PCR检测结果显示,与对照组相比,经各浓度(5、10、20 μmol/L)姜黄素作用48 h后,均可明显抑制黑素细胞c-kit mRNA相对表达量(均P < 0.05)。 结论 低浓度的姜黄素(≤ 20 μmol/L)对黑素细胞无明显细胞毒性,30 μmol/L的姜黄素能够促进黑素细胞的凋亡。姜黄素(≤ 20 μmol/L)可抑制黑素细胞的迁移,并下调人表皮黑素细胞c-kit mRNA的相对表达量。

Abstract:

Li Qilin, Lu Xiaojuan, Niu Mu. Department of Dermatology, Fourth Affiliated Hospital of Jinan University, Guangzhou Red Cross Hospital, Guangzhou 510220, China Corresponding author: Li Qilin, Email: qlli_cn@163.com 【Abstract】 Objective To explore the effect of curcumin on the activity and migration of as well as c-kit mRNA expression in melanocytes. Methods Human epidermal melanocytes were isolated from the prepuce in adolescents and subjected to primary culture. To estimate the effect of curcumin on the proliferative activity of melanocytes, some melanocytes were randomly divided into several groups to be cultured in the MelM-2 medium with or without the presence of 5, 10, 20 or 30 μmol/L curcumin, the MelM-2 medium containing curcumin of 5 - 30 μmol/L served as the drug control groups, and the MelM-2 medium without curcumin served as the blank control group. After 24 and 48 hours of culture, MTS assay was performed to evaluate the proliferative activity of melanocytes. Some cultured melanocytes were randomly divided into 4 groups to be cultured in the MelM-2 medium with 0, 5, 10 and 20 μmol/L curcumin respectively for 48 hours. Then, wound scratch assay was conducted to estimate the migratory activity of melanocytes, and real-time fluorescence-based quantitative PCR to quantify the mRNA expression of c-kit in melanocytes. Statistical analysis was carried out by factorial design analysis of variance (ANOVA), one-way ANOVA and least significant difference (LSD)-t test. Results The proliferative activity of melanocytes was significantly decreased at 24 and 48 hours in the 30-μmol/L curcumin group compared with the negative control group (0.783 ± 0.053 vs. 1.000 ± 0.018 at 24 hours, 0.637 ± 0.015 vs. 0.993 ± 0.064 at 48 hours, both P < 0.05), while no significant differences were observed between the other curcumin groups and the negative control group (all P > 0.05). The 48-hour treatment with curcumin could significantly inhibit the migration of melanocytes in the 5-, 10- and 20-μmol/L curcumin groups compared with the control group (all P < 0.05). The mRNA expression level of c-kit was also significantly reduced at 48 hours in the 5-, 10- and 20-μmol/L curcumin groups compared with the control group (1.799 ± 0.372, 1.539 ± 0.224 and 1.026 ± 0.038 vs. 3.371 ± 0.352, all P < 0.05). Conclusion Curcumin at low concentrations (≤ 20 μmol/L) has no obvious cytotoxicity against melanocytes, but can inhibit the migration of and c-kit mRNA expression in melanocytes, while curcumin at 30 μmol/L can promote the apoptosis of melanocytes.

引用本文

李其林 陆小娟 牛牧. 姜黄素对人表皮黑素细胞活性、迁移及c-kit mRNA表达量的影响[J]. 中华皮肤科杂志, 2015,48(10):705-709. doi: