Quercetin suppress CCL20 by reducing IκBα/STAT3 phosphorylation in TNF-α/IL-17A induced HaCaT cells

作者
Jang-Heub Kim,Min Young Kim,Hyung Seo Hwang
出处
期刊:Journal of Applied Biological Chemistry [The Korean Society for Applied Biological Chemistry]
卷期号:63 (3): 211-219 被引量:1
标识
DOI:10.3839/jabc.2020.029
摘要

Quercetin is a polyphenol compound with excellent antioxidant and anti-inflammatory activity.However, little has been reported about the efficacy of quercetin to control psoriasis.Thus, we aimed to investigate the effect of quercetin to regulate psoriatic dermatitis with HaCaT cell lines activated by TNF-α and IL-17A, which are in vitro psoriasis skin models.When quercetin was treated with TNF-α-activated HaCaT cell line, inflammatory cytokine expressions such as IL-1α, IL-1β and IL-6 were reduced by 49.1±7.14, 42.8±8.16,and 34.5±2.52%,respectively.In addition, mRNA expression levels of IL-8 and CCL20 the chemokines that attract immune cells such as Th17 cells and dendritic cells to the inflammatory reaction site, were also reduced by 38.4±5.83 and 52.9±4.59%compared to the TNF-α treatment group.The expression of proteins KRT6A and KRT16, which was nonspecifically increased in psoriatic skin was also significantly suppressed.Moreover, phosphorylation of IκBα and STAT3 proteins activated by TNFα was also significantly inhibited.After stimulating the HaCaT with IL-17A, known as another psoriasis-inducing cytokine, it was observed that IκBα mRNA expression decreased by 55.8± 5.28%, and STAT3 phosphorylation was downregulated by 36.3±6.81%.Finally, after co-activation by TNF-α/IL-17A, quercetin inhibited all of IL-1α, IL-1β, IL-6, TNF-α and CCL20 gene expression.The above results strongly suggest that quercetin is a material that has not only anti-oxidant and anti-inflammatory activities, but also has an activity in improving psoriasis.Keywords C-C motif chemokine ligand 20 • Keratinocyte • Psoriasis • Quercetin • Signal transducer and activator of transcription 3 서 론 인체 내 피부조직은 외부 충격이나 병원성 미생물 감염

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