Literature DB >> 27718238

Electrophilic nitro-fatty acids suppress allergic contact dermatitis in mice.

A R Mathers1,2, C D Carey1, M E Killeen1, J A Diaz-Perez1, S R Salvatore3, F J Schopfer3, B A Freeman3, L D Falo1,4.   

Abstract

BACKGROUND: Reactions between nitric oxide (NO), nitrite (NO2-), and unsaturated fatty acids give rise to electrophilic nitro-fatty acids (NO2 -FAs), such as nitro oleic acid (OA-NO2 ) and nitro linoleic acid (LNO2 ). Endogenous electrophilic fatty acids (EFAs) mediate anti-inflammatory responses by modulating metabolic and inflammatory signal transduction reactions. Hence, there is considerable interest in employing NO2 -FAs and other EFAs for the prevention and treatment of inflammatory disorders. Thus, we sought to determine whether OA-NO2 , an exemplary nitro-fatty acid, has the capacity to inhibit cutaneous inflammation.
METHODS: We evaluated the effect of OA-NO2 on allergic contact dermatitis (ACD) using an established model of contact hypersensitivity in C57Bl/6 mice utilizing 2,4-dinitrofluorobenzene as the hapten.
RESULTS: We found that subcutaneous (SC) OA-NO2 injections administered 18 h prior to sensitization and elicitation suppresses ACD in both preventative and therapeutic models. In vivo SC OA-NO2 significantly inhibits pathways that lead to inflammatory cell infiltration and the production of inflammatory cytokines in the skin. Moreover, OA-NO2 is capable of enhancing regulatory T-cell activity. Thus, OA-NO2 treatment results in anti-inflammatory effects capable of inhibiting ACD by inducing immunosuppressive responses.
CONCLUSION: Overall, these results support the development of OA-NO2 as a promising therapeutic for ACD and provides new insights into the role of electrophilic fatty acids in the control of cutaneous immune responses potentially relevant to a broad range of allergic and inflammatory skin diseases.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  T regulatory cells; allergic contact dermatitis; contact hypersensitivity; electrophilic fatty acids; nitro-oleic acid

Mesh:

Substances:

Year:  2016        PMID: 27718238      PMCID: PMC5352476          DOI: 10.1111/all.13067

Source DB:  PubMed          Journal:  Allergy        ISSN: 0105-4538            Impact factor:   13.146


  39 in total

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2.  The temporal and spatial dynamics of Foxp3+ Treg cell-mediated suppression during contact hypersensitivity responses in a murine model.

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3.  Anti-vascular endothelial growth factor receptor-2 (Flk-1/KDR) antibody suppresses contact hypersensitivity.

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4.  Nitro-fatty acids and cyclopentenone prostaglandins share strategies to activate the Keap1-Nrf2 system: a study using green fluorescent protein transgenic zebrafish.

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5.  Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice.

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8.  Nrf2-dependent and -independent responses to nitro-fatty acids in human endothelial cells: identification of heat shock response as the major pathway activated by nitro-oleic acid.

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9.  Differential activation of nuclear factor kappa B subunits in a skin dendritic cell line in response to the strong sensitizer 2,4-dinitrofluorobenzene.

Authors:  M Teresa Cruz; Carlos B Duarte; Margarida Gonçalo; Américo Figueiredo; Arsélio P Carvalho; M Celeste Lopes
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10.  Nitro-oleic acid protects against endotoxin-induced endotoxemia and multiorgan injury in mice.

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  8 in total

1.  Topical electrophilic nitro-fatty acids potentiate cutaneous inflammation.

Authors:  Alicia R Mathers; Cara D Carey; Meaghan E Killeen; Sonia R Salvatore; Laura K Ferris; Bruce A Freeman; Francisco J Schopfer; Louis D Falo
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3.  Electrophilic fatty acid nitroalkenes are systemically transported and distributed upon esterification to complex lipids.

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Review 7.  The discovery of nitro-fatty acids as products of metabolic and inflammatory reactions and mediators of adaptive cell signaling.

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Review 8.  Long Chain Fatty Acids as Modulators of Immune Cells Function: Contribution of FFA1 and FFA4 Receptors.

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  8 in total

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