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  • Ergothioneine alleviates se...
    Ko, Hyun Ju; Kim, Jeongtae; Ahn, Meejung; Kim, Jin Hwa; Lee, Geun Soo; Shin, Taekyun

    Experimental cell research, 03/2021, Letnik: 400, Številka: 1
    Journal Article

    Ultraviolet B (UVB) irradiation induces skin damage and photoaging through several deleterious effects, including generation of reactive oxygen species (ROS), apoptosis of epidermal cells, inflammation, and collagen degradation in fibroblasts. Ergothioneine (EGT) is a naturally occurring amino acid with potential biological properties. We evaluated whether EGT protects against UVB-induced photoaging using a keratinocyte/fibroblast co-culture system. Keratinocytes were pretreated with EGT, irradiated with UVB, and co-cultured with fibroblasts. In keratinocytes, ROS production and apoptosis were assessed. We also analyzed the Nrf2/HO-1 pathway, HSP70, proapoptotic proteins, and paracrine cytokines by Western blotting and real-time PCR. Collagen degradation-related genes and senescence were also assessed in fibroblasts. EGT pretreatment of keratinocytes significantly inhibited downregulation of the Nrf2/HO-1 pathway and HSP70, and protected keratinocytes by suppressing production of ROS and cleavage of proapoptotic proteins, including caspase-8 and PARP. Furthermore, EGT significantly reduced the paracrine cytokines, including IL-1β, IL-6, and TNF-α. In co-cultures of fibroblasts with EGT-treated keratinocytes, the expression levels of collagen degradation-related genes and fibroblast senescence were significantly decreased; however, synthesis of procollagen type I was significantly increased. Our results confirm that EGT suppresses the modification of collagen homeostasis in fibroblasts by preventing downregulation of the Nrf2/HO-1 pathway and HSP70 in keratinocytes following UVB irradiation. EGT suppresses changes in collagen homeostasis in fibroblasts by preventing downregulation of the Nrf2/HO-1 pathway and HSP70 in keratinocytes following UVB irradiation. Display omitted •EGT activated Nrf2/HO-1 pathway and HSP70 in UVB-irradiated keratinocytes.•EGT alleviated ROS production, apoptosis, and inflammation in UVB-irradiated keratinocytes.•EGT suppressed senescence and collagen imbalance in fibroblasts by inhibiting the keratinocyte-secreted factors.•EGT suppresses photoaging by UVB irradiation in a keratinocyte/fibroblast co-culture system.