MicroRNA-340 is involved in ultraviolet B-induced pigmentation by regulating the MITF/TYRP1 axis

被引:8
|
作者
Yang, Yi [1 ]
Wei, Xuanjin [1 ]
Bai, Jia [1 ]
Huang, Min [1 ]
Hao, Tian [1 ]
Hao, Yonghong [1 ]
Wang, Yilin [1 ]
Li, Chengxin [1 ]
机构
[1] Peoples Liberat Army Gen Hosp, Dept Dermatol, Med Ctr 1, 28 Fuxing Rd, Beijing 100853, Peoples R China
关键词
Ultraviolet B; pigmentation; miR-340; melanocyte inducing transcription factor (MITF); tyrosine related protein 1 (TYRP1); melanogenesis; microphthalmia-associated transcription factor; HUMAN SKIN PIGMENTATION; TRANSCRIPTION FACTOR; MOLECULAR-BIOLOGY; MELANIN SYNTHESIS; MESSENGER-RNA; MICROPHTHALMIA; EXPRESSION; MITF; TYROSINASE; RESPONSES;
D O I
10.1177/0300060520971510
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective There is growing evidence that ultraviolet B (UVB) irradiation can change the expression profile of microRNAs (miRNAs) in immortalized human epidermal melanocytes (Pig-1). We aimed to investigate the effect of miR-340 on regulating UVB-induced pigmentation. Methods Real-time quantitative PCR (qRT-PCR) was used to evaluate the expression of miR-340 in Pig-1 cells. Immunoblotting analysis, qRT-PCR, and luciferase reporter assays were used to detect the potential target of miR-340. The sodium hydroxide dissolution assay was used to assess the effect of miR-340 on changes in melanin content. Results Expression of miR-340 was reduced in human Pig-1 cells after UVB irradiation. We found a negative correlation between miR-340 and melanocyte inducing transcription factor (MITF) in Pig-1 cells after UVB irradiation. Knockdown and overexpression of MITF in Pig-1 cells down- and upregulated melanogenesis, respectively. Overexpression of miR-340 inhibited MITF expression, reduced the amount of melanin, and suppressed expression of multiple key molecules involved in the pigment synthesis pathway, whereas knockdown of miR-340 showed the opposite results. Conclusions Our results showed that miR-340 inhibited melanogenesis by regulating the downstream molecules of MITF and its signaling pathways, suggested that miRNA-340 may be a new target for the clinical treatment of UVB-induced pigmentation.
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页数:13
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