Intraocular fatty acids induce reinforcement of barrier functions on the outer blood-retinal barrier.

Extracellular flux analysis Fatty acids Outer blood-retinal barrier Retinal pigment epithelium

Journal

Prostaglandins, leukotrienes, and essential fatty acids
ISSN: 1532-2823
Titre abrégé: Prostaglandins Leukot Essent Fatty Acids
Pays: Scotland
ID NLM: 8802730

Informations de publication

Date de publication:
08 Aug 2024
Historique:
received: 29 05 2024
revised: 17 07 2024
accepted: 06 08 2024
medline: 12 8 2024
pubmed: 12 8 2024
entrez: 11 8 2024
Statut: aheadofprint

Résumé

The aim of the present study was to elucidate unknown effects of intraocular fatty acids (ioFAs) including palmitic acid (C16:0), stearic acid (C18:0), oleic acid (C18:1), linoleic acid (C18:2), arachidonic acid (C20:4), eicosapentaenoic acid (EPA, C20:5) and docosahexaenoic acid (DHA, C22:6) on the outer blood-retinal barrier (oBRB). For this purpose, human retinal pigment epithelium cell line ARPE19 was subjected to analyses for evaluating the following biological phenotypes: (1) cell viability, (2) cellular metabolic functions, (3) barrier functions by trans-epithelial electrical resistance (TEER), and (4) expression of tight junction (TJ) molecules. In the presence of 100 nM ioFAs, no significant effects on cell viability of ARPE19 cells was observed. While treatment with EPA or DHA tended to reduce non-mitochondrial oxygen consumption, most indices in mitochondrial functions were not markedly affected by treatment with ioFAs in ARPE19 cells. On the other hand, ioFAs except for palmitic acid and stearic acid significantly increased basal extracellular acidification rates, suggesting activated glycolysis or increased lactate production. Interestingly, TEER values of planar ARPE19 monolayer were significantly increased by treatment any ioFAs. Consistently, gene expression levels of TJ proteins were increased by treatment with ioFAs. Collectively, the findings presented herein suggest that ioFAs may contribute to reinforcement of barrier functions of the oBRB albeit there are some differences in biological effects depending on the type of ioFAs.

Identifiants

pubmed: 39128394
pii: S0952-3278(24)00031-0
doi: 10.1016/j.plefa.2024.102637
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102637

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Auteurs

Nami Nishikiori (N)

Department of Ophthalmology, Sapporo Medical University School of Medicine, Japan.

Megumi Watanabe (M)

Department of Ophthalmology, Sapporo Medical University School of Medicine, Japan.

Tatsuya Sato (T)

Department ofCardiovascular, Renal and Metabolic Medicine, Sapporo Medical University School of Medicine, Japan; Department ofCellular Physiology and Signal Transduction, Sapporo Medical University School of Medicine, Japan.

Araya Umetsu (A)

Department of Ophthalmology, Sapporo Medical University School of Medicine, Japan.

Megumi Higashide (M)

Department of Ophthalmology, Sapporo Medical University School of Medicine, Japan.

Masato Furuhashi (M)

Department ofCardiovascular, Renal and Metabolic Medicine, Sapporo Medical University School of Medicine, Japan.

Hiroshi Ohguro (H)

Department of Ophthalmology, Sapporo Medical University School of Medicine, Japan. Electronic address: ooguro@sapmed.ac.jp.

Classifications MeSH