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Gentiana lutea Extract Modulates Ceramide Synthesis in Primary and Psoriasis-Like Keratinocytes
F. Gendrisch, A. Nováčková, M. Sochorová, B. Haarhaus, K. Vávrová, CM. Schempp, U. Wölfle
Language English Country Switzerland
Document type Journal Article
Grant support
ZF4399503MD7
Federal Ministry for Economic Affairs and Energy
19-09135J
the Czech Science Foundation
SVV 260 401
Charles University
NLK
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- MeSH
- Ceramides metabolism MeSH
- Fatty Acid Elongases genetics metabolism MeSH
- Gentiana chemistry MeSH
- Keratinocytes cytology drug effects metabolism MeSH
- Cells, Cultured MeSH
- Humans MeSH
- Membrane Proteins genetics metabolism MeSH
- Lipid Metabolism drug effects MeSH
- Eye Proteins genetics metabolism MeSH
- Primary Cell Culture MeSH
- Psoriasis genetics metabolism MeSH
- Gene Expression Regulation drug effects MeSH
- Plant Extracts chemistry pharmacology MeSH
- Sphingosine N-Acyltransferase genetics metabolism MeSH
- Case-Control Studies MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Gentiana lutea is a bitter herb that is traditionally used to improve gastric disorders. Recently, we have shown that Gentiana lutea extract (GE) also modulates the lipid metabolism of human keratinocytes in vitro and in vivo. In the present study, we investigated the role of GE on ceramide synthesis in human primary keratinocytes (HPKs) and psoriasis-like keratinocytes. We could demonstrate that GE increased the concentrations of glucosylceramides and the ceramide AS/AdS subclass without affecting the overall ceramide content in HPKs. The expression of ceramide synthase 3 (CERS3) and elongases (ELOVL1 and 4) was reduced in psoriasis lesions compared to healthy skin. Psoriasis-like HPKs, generated by stimulating HPKs with cytokines that are involved in the pathogenesis of psoriasis (IL-17, TNF-α, IL-22 and IFN-γ) showed increased levels of IL-6, IL-8 and increased expression of DEFB4A, as well as decreased expression of ELOVL4. The treatment with GE partly rescued the reduced expression of ELOVL4 in psoriasis-like HPKs and augmented CERS3 expression. This study has shown that GE modulates ceramide synthesis in keratinocytes. Therefore, GE might be a novel topical treatment for skin diseases with an altered lipid composition such as psoriasis.
References provided by Crossref.org
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