2-Pentadecyl-2-oxazoline inhibits lipopolysaccharide-induced microglia activation interfering with TLR4 signaling.


Journal

Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521

Informations de publication

Date de publication:
15 Dec 2023
Historique:
received: 14 06 2023
revised: 24 10 2023
accepted: 01 11 2023
medline: 4 12 2023
pubmed: 13 11 2023
entrez: 12 11 2023
Statut: ppublish

Résumé

2-Pentadecyl-2-oxazoline (PEA-OXA), the oxazoline derivative of N-palmitoylethanolamine, exerts anti-inflammatory activity; however, very little is known about the molecular mechanisms underlying this effect. Here, we tested the anti-neuroinflammatory effect of PEA-OXA in primary microglia and we also investigated the possible interaction of the molecule with the Toll-like receptor 4 (TLR4)-myeloid differentiation protein-2 (MD-2) complex. The anti-inflammatory effect of PEA-OXA was analyzed by measuring the expression and release of pro-inflammatory mediators in primary microglia by real-time PCR and ELISA, respectively. The effect of PEA-OXA on the activation of TLR4 signaling was assessed using two stably TLR4-transfected cell lines (i.e., HEK-293 and Ba/F3 cells). Finally, the putative binding mode of PEA-OXA to TLR4-MD-2 was investigated by molecular docking simulations. Treatment with PEA-OXA resulted in the following effects: (i) it down-regulated gene expression of several pro-inflammatory molecules and the secretion of pro-inflammatory cytokines in LPS stimulated microglia cells; (ii) it did not prevent microglia activation after stimulation with TLR2 ligands; (iii) it prevented TLR4/NF-κB activation triggered by LPS in HEK-Blue™ hTLR4 cells; and (iv) it interfered with the binding of LPS to TLR4-MD-2 complex. Furthermore, molecular docking studies suggested that PEA-OXA could bind MD-2 with a 1:3 (MD-2/PEA-OXA) stoichiometry. We show for the first time that the anti-neuroinflammatory effect of PEA-OXA involves its activity against TLR4 signaling, making this molecule a valuable tool for the development of new compounds directed to control neuroinflammation via inhibiting TLR4 signaling.

Identifiants

pubmed: 37952834
pii: S0024-3205(23)00877-9
doi: 10.1016/j.lfs.2023.122242
pii:
doi:

Substances chimiques

2-pentadecyl-2-oxazoline 0
Lipopolysaccharides 0
Toll-Like Receptor 4 0
Anti-Inflammatory Agents 0
NF-kappa B 0
TLR4 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122242

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest MF was employed by the company Epitech Group SpA. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Auteurs

Laura Facci (L)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Chiara Bolego (C)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Chiara Chemello (C)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Reem Yasser (R)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Mariella Fusco (M)

Scientific Information and Documentation Center, Epitech Group SpA, Padua, Italy.

Massimo Barbierato (M)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Pietro Giusti (P)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Stefano Moro (S)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy.

Morena Zusso (M)

Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padua, Italy. Electronic address: morena.zusso@unipd.it.

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Classifications MeSH