Linoleic Acid Induces Metabolic Reprogramming and Inhibits Oxidative and Inflammatory Effects in Keratinocytes Exposed to UVB Radiation.
Keratinocytes
/ metabolism
Ultraviolet Rays
/ adverse effects
Humans
Linoleic Acid
/ pharmacology
Oxidative Stress
/ drug effects
Reactive Oxygen Species
/ metabolism
Inflammation
/ metabolism
Glutathione
/ metabolism
HaCaT Cells
Signal Transduction
/ drug effects
Cell Line
Phosphatidylinositol 3-Kinases
/ metabolism
Oxidation-Reduction
/ drug effects
Cyclooxygenase 2
/ metabolism
Proto-Oncogene Proteins c-akt
/ metabolism
Metabolic Reprogramming
keratinocyte
linoleic acid
photodamage
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
26 Sep 2024
26 Sep 2024
Historique:
received:
23
08
2024
revised:
20
09
2024
accepted:
24
09
2024
medline:
16
10
2024
pubmed:
16
10
2024
entrez:
16
10
2024
Statut:
epublish
Résumé
Linoleic acid (LA), the primary ω-6 polyunsaturated fatty acid (PUFA) found in the epidermis, plays a crucial role in preserving the integrity of the skin's water permeability barrier. Additionally, vegetable oils rich in LA have been shown to notably mitigate ultraviolet (UV) radiation-induced effects, including the production of reactive oxygen species (ROS), cellular damage, and skin photoaging. These beneficial effects are primarily ascribed to the LA in these oils. Nonetheless, the precise mechanisms through which LA confers protection against damage induced by exposure to UVB radiation remain unclear. This study aimed to examine whether LA can restore redox and metabolic equilibria and to assess its influence on the inflammatory response triggered by UVB radiation in keratinocytes. Flow cytometry analysis unveiled the capacity of LA to diminish UVB-induced ROS levels in HaCaT cells. GC/MS-based metabolomics highlighted significant metabolic changes, especially in carbohydrate, amino acid, and glutathione (GSH) metabolism, with LA restoring depleted GSH levels post-UVB exposure. LA also upregulated PI3K/Akt-dependent GCLC and GSS expression while downregulating COX-2 expression. These results suggest that LA induces metabolic reprogramming, protecting against UVB-induced oxidative damage by enhancing GSH biosynthesis via PI3K/Akt signaling. Moreover, it suppresses UVB-induced COX-2 expression in HaCaT cells, making LA treatment a promising strategy against UVB-induced oxidative and inflammatory damage.
Identifiants
pubmed: 39408715
pii: ijms251910385
doi: 10.3390/ijms251910385
pii:
doi:
Substances chimiques
Linoleic Acid
9KJL21T0QJ
Reactive Oxygen Species
0
Glutathione
GAN16C9B8O
Phosphatidylinositol 3-Kinases
EC 2.7.1.-
Cyclooxygenase 2
EC 1.14.99.1
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Fondo Nacional de Desarrollo Científico y Tecnológico (FONDECYT)
ID : 11220320