α-Linolenic acid and linoleic acid modulate the lipidome and the skin barrier of a tissue-engineered skin model.

Bioactive lipid mediators Lipidomics Polyunsaturated fatty acids Skin barrier function Skin substitutes Tissue engineering

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 03 2022
Historique:
received: 02 07 2021
revised: 15 11 2021
accepted: 16 11 2021
pubmed: 23 11 2021
medline: 5 3 2022
entrez: 22 11 2021
Statut: ppublish

Résumé

Polyunsaturated fatty acids (PUFAs) play an important role in the establishment and the maintenance of the skin barrier function. However, the impact of their derived lipid mediators remains unclear. Skin substitutes were engineered according to the self-assembly method with a culture medium supplemented with 10 μM of both α-linolenic acid (ALA) and linoleic acid (LA). The supplementation with ALA and LA decreased testosterone absorption through a tissue-engineered reconstructed skin model, thus indicating an improved skin barrier function following supplementation. The exogenously provided fatty acids were incorporated into the phospholipid and triglyceride fractions of the skin substitutes. Indeed, the dual supplementation increased the levels of eicosapentaenoic acid (EPA) (15-fold), docosapentaenoic acid (DPA) (3-fold), and LA (1.5-fold) in the epidermal phospholipids while it increased the levels of ALA (>20-fold), DPA (3-fold) and LA (1.5-fold) in the epidermal triglycerides. The bioactive lipid mediator profile of the skin substitutes, including prostaglandins, hydroxy-fatty acids, N-acylethanolamines and monoacylglycerols, was next analyzed using liquid chromatography-tandem mass spectrometry. The lipid supplementation further modulated bioactive lipid mediator levels of the reconstructed skin substitutes, leading to a lipid mediator profile more representative of the one found in normal human skin. These findings show that an optimized supply of PUFAs via culture media is essential for the establishment of improved barrier function in vitro. STATEMENT OF SIGNIFICANCE: Supplementation of the culture medium with 10 μM of both α-linolenic acid (ALA) and linoleic acid (LA) improved the skin barrier function of a tissue-engineered skin model. The exogenously provided fatty acids were incorporated into the phospholipid and triglyceride fractions of the skin substitutes and further modulated bioactive lipid mediator levels, including prostaglandins, hydroxy-fatty acids, N-acylethanolamines and monoacylglycerols. These findings highlight the important role of ALA and LA in skin homeostasis and show that an optimized supply of polyunsaturated fatty acids via culture media is essential for the establishment of improved barrier function in vitro.

Identifiants

pubmed: 34808417
pii: S1742-7061(21)00770-4
doi: 10.1016/j.actbio.2021.11.021
pii:
doi:

Substances chimiques

alpha-Linolenic Acid 0RBV727H71
Linoleic Acid 9KJL21T0QJ
Eicosapentaenoic Acid AAN7QOV9EA

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

261-274

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare no competing interests

Auteurs

Mélissa Simard (M)

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe médecine régénératrice, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, G1J 1Z4, Canada; Faculté de pharmacie de l'Université Laval, Québec, QC, G1J 1A4, Canada.

Andréa Tremblay (A)

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe médecine régénératrice, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, G1J 1Z4, Canada; Faculté de pharmacie de l'Université Laval, Québec, QC, G1J 1A4, Canada.

Sophie Morin (S)

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe médecine régénératrice, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, G1J 1Z4, Canada; Faculté de pharmacie de l'Université Laval, Québec, QC, G1J 1A4, Canada.

Cyril Martin (C)

Centre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec, QC, G1V 4G5, Canada; Canada Excellence Research Chair on the Microbiome-Endocannabinoidome Axis in Metabolic Health (CERC-MEND), Université Laval, Québec, QC, Canada.

Pierre Julien (P)

Département de médecine, Faculté de médecine de l'Université Laval, Québec, QC, G1V 0A6, Canada; Axe Endocrinologie et Néphrologie, Centre de recherche du CHU de Québec, Université Laval, Québec, QC, G1J 1A4, Canada.

Julie Fradette (J)

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe médecine régénératrice, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, G1J 1Z4, Canada; Département de chirurgie, Faculté de médecine de l'Université Laval, Québec, QC, G1V 0A6, Canada.

Nicolas Flamand (N)

Centre de recherche de l'Institut universitaire de cardiologie et de pneumologie de Québec, QC, G1V 4G5, Canada; Canada Excellence Research Chair on the Microbiome-Endocannabinoidome Axis in Metabolic Health (CERC-MEND), Université Laval, Québec, QC, Canada.

Roxane Pouliot (R)

Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Axe médecine régénératrice, Centre de recherche du CHU de Québec-Université Laval, Québec, QC, G1J 1Z4, Canada; Faculté de pharmacie de l'Université Laval, Québec, QC, G1J 1A4, Canada. Electronic address: roxane.pouliot@ulaval.pha.ca.

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Classifications MeSH