Department of Anatomy and Cell Biology, School of Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Biocenter, Gyeonggido Business & Science Accelerator, Suwon, Republic of Korea.
J Invest Dermatol. 2021 Oct;141(10):2459-2469. doi: 10.1016/j.jid.2021.01.037. Epub 2021 Apr 3.
The keratinocytes in UV-irradiated skin produce and secrete α-melanocyte-stimulating hormone. α-Melanocyte-stimulating hormone upregulates the expression of MITF in melanocytes through the cAMP‒protein kinase A‒CREB signaling pathway. Thereafter, MITF induces the expression of melanogenic genes, including the tyrosinase gene TYR and TYRP-1 and TYRP-2 genes, which leads to the synthesis and accumulation of melanin. In this study, we examined whether MITF basic region-derived tripeptides can bind to the DNA-binding domain of MITF and inhibit MITF-induced melanogenesis through the inhibition of MITF‒DNA binding. MITF-KGR, a representative MITF-derived tripeptide, suppressed the transcriptional activity of MITF by disrupting its binding to the promoter region of the target genes, which resulted in the inhibition of skin epidermis thickness and melanin synthesis in vivo and in vitro. Our results indicate that MITF-KGR exerts an inhibitory effect on melanogenesis by targeting MITF.
受紫外线照射的皮肤中的角质形成细胞会产生和分泌 α-促黑素细胞激素。α-促黑素细胞激素通过 cAMP-蛋白激酶 A-CREB 信号通路上调黑素细胞中 MITF 的表达。此后,MITF 诱导包括酪氨酸酶基因 TYR 和 TYRP-1 和 TYRP-2 基因在内的黑色素生成基因的表达,导致黑色素的合成和积累。在这项研究中,我们检查了 MITF 基本区域衍生的三肽是否可以与 MITF 的 DNA 结合域结合,并通过抑制 MITF-DNA 结合来抑制 MITF 诱导的黑色素生成。MITF-KGR 是代表性的 MITF 衍生三肽,通过破坏其与靶基因启动子区域的结合来抑制 MITF 的转录活性,从而抑制体内和体外皮肤表皮厚度和黑色素合成。我们的结果表明,MITF-KGR 通过靶向 MITF 对黑色素生成发挥抑制作用。