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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
Jazyk angličtina Země Švýcarsko
Typ dokumentu časopisecké články
Grantová podpora
ZF4399503MD7
Federal Ministry for Economic Affairs and Energy
19-09135J
the Czech Science Foundation
SVV 260 401
Charles University
NLK
Directory of Open Access Journals
od 1997
Free Medical Journals
od 1997
PubMed Central
od 2001
Europe PubMed Central
od 2001
ProQuest Central
od 1997-01-01
Open Access Digital Library
od 1997-01-01
Medline Complete (EBSCOhost)
od 2009-03-01
Health & Medicine (ProQuest)
od 1997-01-01
- MeSH
- ceramidy metabolismus MeSH
- elongasy mastných kyselin genetika metabolismus MeSH
- Gentiana chemie MeSH
- keratinocyty cytologie účinky léků metabolismus MeSH
- kultivované buňky MeSH
- lidé MeSH
- membránové proteiny genetika metabolismus MeSH
- metabolismus lipidů účinky léků MeSH
- oční proteiny genetika metabolismus MeSH
- primární buněčná kultura MeSH
- psoriáza genetika metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- rostlinné extrakty chemie farmakologie MeSH
- sfingosin-N-acyltransferasa genetika metabolismus MeSH
- studie případů a kontrol MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články 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.
Citace poskytuje Crossref.org
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