Olive‐Oil‐Derived Polyphenols Effectively Attenuate Inflammatory Responses of Human Keratinocytes by Interfering with the NF‐κB Pathway

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Scope: Extra virgin olive oil (EVOO) is rich in phenolic compounds, including hydroxytyrosol (HTy) and hydroxytyrosyl acetate (HTy‐Ac), which have presented multiple beneficial properties. Their impact on inflammatory responses in human keratinocytes and modes of action have not been addressed yet. Methods and results: Primary human keratinocytes are pretreated with HTy‐Ac or HTy for 30 min and stimulated with IL‐1β or Toll‐like receptor 3 ligand (TLR3‐l). Thymic stromal lymphopoietin (TSLP), measured by ELISA, is attenuated by both polyphenols in a dose‐dependent manner. The expression of several inflammation‐related genes, including distinct TSLP isoforms and IL‐8, are assessed by quantitative RT‐PCR and likewise inhibited by HTy‐Ac/HTy. Mechanistically, EVOO phenols counteracts IκB degradation and translocation of NF‐κB to the nucleus, a transcription factor of essential significance to TSLP and IL‐8 transcriptional activity; this is evidenced by immunoblotting. Accordingly, NF‐κB recruitment to critical binding sites in the TSLP and IL‐8 promoter is impeded in the presence of HTy‐Ac/HTy, as demonstrated by chromatin immunoprecipitation. Promoter reporter assays finally reveal that the neutralizing effect on NF‐κB induction has functional consequences, resulting in reduced NF‐κB‐directed transcription. Conclusion: EVOO phenols afford protection from inflammation in human keratinocytes by interference with the NF‐κB pathway.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Olive‐Oil‐Derived Polyphenols Effectively Attenuate Inflammatory Responses of Human Keratinocytes by Interfering with the NF‐κB Pathway ; volume:63 ; number:21 ; year:2019 ; extent:10
Molecular nutrition & food research ; 63, Heft 21 (2019) (gesamt 10)

Urheber
Aparicio‐Soto, Marina
Redhu, Davender
Sánchez‐Hidalgo, Marina
Fernández‐Bolaños, José G.
Alarcón‐de‐la‐Lastra, Catalina
Worm, Margitta
Babina, Magda

DOI
10.1002/mnfr.201900019
URN
urn:nbn:de:101:1-2022072008010038083724
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
15.08.2025, 07:35 MESZ

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Beteiligte

  • Aparicio‐Soto, Marina
  • Redhu, Davender
  • Sánchez‐Hidalgo, Marina
  • Fernández‐Bolaños, José G.
  • Alarcón‐de‐la‐Lastra, Catalina
  • Worm, Margitta
  • Babina, Magda

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