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Role of epidermal γδ T‐cell‐derived interleukin 13 in the skin‐whitening effect of Ginsenoside F1
Authors:Jiyeon Han  Eunkyung Lee  EunJoo Kim  Myung Hun Yeom  Ohsang Kwon  Tae Hong Yoon  Tae Ryong Lee  Kwangmi Kim
Affiliation:1. R&D Unit, AmorePacific Corporation, , Yongin‐si, Gyeonggi‐do, Korea;2. Institute of Dermatological Science, Medical Research Center, Seoul National University, , Seoul, Korea;3. Department of Dermatology, College of Medicine, Seoul National University, , Seoul, Korea;4. College of Pharmacy, Dankook University, , Cheonan‐si, Chungnam, Korea
Abstract:
Ginsenoside F1 (GF1) is a metabolite of ginsenoside Rg1. Although GF1 has several benefits for skin physiology, the effect of GF1 on skin pigmentation has not been reported. We found that a cream containing 0.1% GF1 showed a significant whitening effect on artificially tanned human skin after 8 weeks of application. However, GF1 did not inhibit mRNA expression of tyrosinase or dopachrome tautomerase (DCT) in normal human epidermal melanocytes (NHEMs) or cocultured NHEMs/normal human epidermal keratinocytes. Interestingly, GF1 enhanced production of interleukin 13 (IL‐13) from human epidermal γδ T cells. IL‐13 significantly reduced the mRNA expression and protein amount of both tyrosinase and DCT and reduced melanin synthesis activities in NHEMs, resulting in visible brightening of NHEM pellet. These results suggest that enhancement of IL‐13 production by GF1 from epidermal γδ T cells might play a role in the skin‐whitening effect of GF1 via the suppression of tyrosinase and DCT.
Keywords:epidermal γ  δ   T cells  ginsenoside F1  interleukin 13  skin whitening
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