Journal
ANNALS OF DERMATOLOGY
Volume 29, Issue 1, Pages 20-25Publisher
KOREAN DERMATOLOGICAL ASSOC
DOI: 10.5021/ad.2017.29.1.20
Keywords
Biomarkers; Insulin-like growth factor-1; Sebum
Categories
Funding
- Amore-Pacific Corporation
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Background: Acne vulgaris has been linked to the Western diet. Hyperglycemic diet increases insulin and insulin-like growth factor (IGF)-1. Deeper insights into IGF-1-mediated signal pathway are critical importance to understand the impact of Western diet. Objective: We investigated the effect of IGF-1 on the expression of inflammatory biomarkers and sebum production in cultured sebocytes. Methods: Polymerase chain reaction and enzyme-linked immunosorbent assay were performed to measure changes in the expression of inflammatory biomarkers including interleukin (IL)-1 beta, IL-6, IL-8, tumor necrosis factor (TNF)-alpha, nuclear factor kappa -light-chain-enhancer of activated B cells (NF-kappa B), IGF1R, IGFBP2, sterol response element-binding protein (SREBP), and phosphatidylinosito1-4,5-bisphosphate 3-kinase, catalytic subunit alpha (PI3KCA) after the treatment of cultured sebocytes with 10(-7)M or 10(-5)M IGF-1. Sebum production was evaluated after the treatment of cultured sebocytes with 10(-7)M or 10(-5)M IGF-1 using lipid analysis. Results: The expression levels of IL-1 beta, IL-6, IL-8, and TNF-alpha in cultured sebocytes after treatment with 10(-7)M or 10(-5)M IGF-1 were increased. Increased gene expression levels of NF-kappa B in cultured sebocytes were also shown after 10(-7) M or 10(-5) M IGF-1 treatments. Gene expression of these inflammatory biomarkers was decreased after 10(-7)M or 10(-5)M IGF-1 treatment in the presence of 100 nM NF-kappa B inhibitor. Treatment with 10(-7)M or 10(-5)M IGF-1 increased the gene expression levels of IGF1R, IGFBP2, SREBP and PI3KCA in cultured sebocytes. Sebum production from cultured sebocytes treated with 10(-7) M or 10(-5) M IGF-1 was also increased. Conclusion: It is suggestive that IGF-1 might be involved in the pathogenesis of acne by increasing both expression of inflammatory biomarkers and also sebum production in sebocytes.
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