4.7 Article

Korean Red Ginseng Attenuates Particulate Matter-Induced Senescence of Skin Keratinocytes

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ANTIOXIDANTS
卷 12, 期 8, 页码 -

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MDPI
DOI: 10.3390/antiox12081516

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fine particulate matter; skin cellular senescence; Korean red ginseng; epigenetic alteration

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This study investigates whether Korean red ginseng (KRG) can inhibit PM2.5-induced senescence in skin keratinocytes. The results show that KRG can suppress PM2.5-induced cellular senescence and protect skin keratinocytes by epigenetic regulation of the p16(INK4A) gene.
Skin is a direct target of fine particulate matter (PM2.5), as it is constantly exposed. Herein, we investigate whether Korean red ginseng (KRG) can inhibit PM2.5-induced senescence in skin keratinocytes. PM2.5-treated human keratinocyte cell lines and normal human epidermal keratinocytes showed characteristics of cellular senescence, including flat and enlarged forms; however, KRG suppressed them in both cell types. Moreover, while cells exposed to PM2.5 showed a higher level of p16( )(INK4A)expression (a senescence inducer), KRG inhibited its expression. Epigenetically, KRG decreased the expression of the ten-eleven translocation (TET) enzyme, a DNA demethylase induced by PM2.5, and increased the expression of DNA methyltransferases suppressed by PM2.5, resulting in the decreased methylation of the p16(INK4A) promoter region. Additionally, KRG decreased the expression of mixed-lineage leukemia 1 (MLL1), a histone methyltransferase, and histone acetyltransferase 1 (HAT1) induced by PM2.5. Contrastingly, KRG increased the expression of the enhancer of zeste homolog 2, a histone methyltransferase, and histone deacetyltransferase 1 reduced by PM2.5. Furthermore, KRG decreased TET1, MLL1, and HAT1 binding to the p16INK4A promoter, corresponding with the decreased mRNA expression of p16(INK4A). These results suggest that KRG exerts protection against the PM2.5-induced senescence of skin keratinocytes via the epigenetic regulation of p16(INK4A).

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