Department of Otolaryngology, Ajou University School of Medicine, Suwon, Korea.
Arch Dermatol Res. 2010 May;302(4):301-6. doi: 10.1007/s00403-009-1012-0. Epub 2009 Dec 23.
Development of vitiligo-like hypopigmentary lesions associated with topical imiquimod has been reported. We hypothesized that mode of action of imiquimod in melanocytes may include triggering of apoptosis resulted in loss of cells, which may be a possible mechanism of imiquimod-induced hypopigmentary lesions. Therefore, we investigated whether imiquimod induces apoptosis of human melanocytes and also whether it modulates expression of apoptosis-related molecules in human melanocytes. Imiquimod treatment induced apoptosis of melanocytes, which was observed by TUNEL assay and Hoechst 33258 staining. Imiquimod-induced apoptosis was further shown by measuring mitochondrial membrane potential in melanocytes. The apoptotic activity of imiquimod was associated with caspase-3, Bcl-2 and mitogen-activated protein kinase expression in melanocytes. These results indicated that imiquimod induces apoptosis of melanocytes. These findings may provide a clue to understand pathogenesis of imiquimod-induced vitiligo-like hypopigmentary lesions.
已有报道称,咪喹莫特外用可导致类似白癜风的色素减退性病变。我们假设咪喹莫特在黑素细胞中的作用模式可能包括触发细胞凋亡导致细胞丢失,这可能是咪喹莫特诱导色素减退性病变的一种可能机制。因此,我们研究了咪喹莫特是否诱导人黑素细胞凋亡,以及它是否调节人黑素细胞中与凋亡相关的分子表达。TUNEL 检测和 Hoechst 33258 染色观察到咪喹莫特处理诱导黑素细胞凋亡。通过测量黑素细胞中线粒体膜电位进一步显示咪喹莫特诱导的细胞凋亡。咪喹莫特的凋亡活性与黑素细胞中 caspase-3、Bcl-2 和丝裂原活化蛋白激酶的表达有关。这些结果表明咪喹莫特诱导黑素细胞凋亡。这些发现可能为理解咪喹莫特诱导的白癜风样色素减退性病变的发病机制提供线索。