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Nitro-oleic acid inhibits vascular endothelial inflammatory responses and the endothelial-mesenchymal transition
G. Ambrozova, T. Fidlerova, H. Verescakova, A. Koudelka, TK. Rudolph, SR. Woodcock, BA. Freeman, L. Kubala, M. Pekarova,
Language English Country Netherlands
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
- MeSH
- Endothelium, Vascular cytology drug effects metabolism MeSH
- Endothelial Cells drug effects metabolism MeSH
- Epithelial-Mesenchymal Transition * MeSH
- Oleic Acids pharmacology MeSH
- Humans MeSH
- Macrophages drug effects metabolism MeSH
- MAP Kinase Signaling System MeSH
- Mice MeSH
- NF-kappa B metabolism MeSH
- Smad Proteins metabolism MeSH
- Transforming Growth Factor beta pharmacology MeSH
- STAT Transcription Factors metabolism MeSH
- Inflammation metabolism MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
BACKGROUND: Inflammatory-mediated pathological processes in the endothelium arise as a consequence of the dysregulation of vascular homeostasis. Of particular importance are mediators produced by stimulated monocytes/macrophages inducing activation of endothelial cells (ECs). This is manifested by excessive soluble pro-inflammatory mediator production and cell surface adhesion molecule expression. Nitro-fatty acids are endogenous products of metabolic and inflammatory reactions that display immuno-regulatory potential and may represent a novel therapeutic strategy to treat inflammatory diseases. The purpose of our study was to characterize the effects of nitro-oleic acid (OA-NO2) on inflammatory responses and the endothelial-mesenchymal transition (EndMT) in ECs that is a consequence of the altered healing phase of the immune response. METHODS: The effect of OA-NO2 on inflammatory responses and EndMT was determined in murine macrophages and murine and human ECs using Western blotting, ELISA, immunostaining, and functional assays. RESULTS: OA-NO2 limited the activation of macrophages and ECs by reducing pro-inflammatory cytokine production and adhesion molecule expression through its modulation of STAT, MAPK and NF-κB-regulated signaling. OA-NO2 also decreased transforming growth factor-β-stimulated EndMT and pro-fibrotic phenotype of ECs. These effects are related to the downregulation of Smad2/3. CONCLUSIONS: The study shows the pleiotropic effect of OA-NO2 on regulating EC-macrophage interactions during the immune response and suggests a role for OA-NO2 in the regulation of vascular endothelial immune and fibrotic responses arising during chronic inflammation. GENERAL SIGNIFICANCE: These findings propose the OA-NO2 may be useful as a novel therapeutic agent for treatment of cardiovascular disorders associated with dysregulation of the endothelial immune response.
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- $a Ambrozova, Gabriela $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic. $7 gn_A_00005405
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- $a Nitro-oleic acid inhibits vascular endothelial inflammatory responses and the endothelial-mesenchymal transition / $c G. Ambrozova, T. Fidlerova, H. Verescakova, A. Koudelka, TK. Rudolph, SR. Woodcock, BA. Freeman, L. Kubala, M. Pekarova,
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- $a BACKGROUND: Inflammatory-mediated pathological processes in the endothelium arise as a consequence of the dysregulation of vascular homeostasis. Of particular importance are mediators produced by stimulated monocytes/macrophages inducing activation of endothelial cells (ECs). This is manifested by excessive soluble pro-inflammatory mediator production and cell surface adhesion molecule expression. Nitro-fatty acids are endogenous products of metabolic and inflammatory reactions that display immuno-regulatory potential and may represent a novel therapeutic strategy to treat inflammatory diseases. The purpose of our study was to characterize the effects of nitro-oleic acid (OA-NO2) on inflammatory responses and the endothelial-mesenchymal transition (EndMT) in ECs that is a consequence of the altered healing phase of the immune response. METHODS: The effect of OA-NO2 on inflammatory responses and EndMT was determined in murine macrophages and murine and human ECs using Western blotting, ELISA, immunostaining, and functional assays. RESULTS: OA-NO2 limited the activation of macrophages and ECs by reducing pro-inflammatory cytokine production and adhesion molecule expression through its modulation of STAT, MAPK and NF-κB-regulated signaling. OA-NO2 also decreased transforming growth factor-β-stimulated EndMT and pro-fibrotic phenotype of ECs. These effects are related to the downregulation of Smad2/3. CONCLUSIONS: The study shows the pleiotropic effect of OA-NO2 on regulating EC-macrophage interactions during the immune response and suggests a role for OA-NO2 in the regulation of vascular endothelial immune and fibrotic responses arising during chronic inflammation. GENERAL SIGNIFICANCE: These findings propose the OA-NO2 may be useful as a novel therapeutic agent for treatment of cardiovascular disorders associated with dysregulation of the endothelial immune response.
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- $a Fidlerova, Tana $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic.
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- $a Verescakova, Hana $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic; Faculty of Science, Institute of Experimental Biology, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic.
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- $a Koudelka, Adolf $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic; Faculty of Science, Institute of Experimental Biology, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic.
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- $a Rudolph, Tanja K $u Faculty of Science, Institute of Experimental Biology, Masaryk University, Kamenice 5, 625 00 Brno, Czech Republic; Heart Centre, University Hospital of Cologne, Kerpener Str. 62, 50937 Cologne, Germany.
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- $a Woodcock, Steven R $u Department of Pharmacology and Chemical Biology, University of Pittsburgh, 4200 Fifth Ave, Pittsburgh, PA 15260, USA.
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- $a Kubala, Lukas $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic; International Clinical Research Center - Center of Biomolecular and Cellular Engineering, St. Anne's University Hospital, Pekarska 53, 656 91, Brno, Czech Republic.
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- $a Pekarova, Michaela $u Department of Free Radical Pathophysiology, Institute of Biophysics, Academy of Sciences of the Czech Republic, Kralovopolska 135, 612 65, Brno, Czech Republic; International Clinical Research Center - Center of Biomolecular and Cellular Engineering, St. Anne's University Hospital, Pekarska 53, 656 91, Brno, Czech Republic. Electronic address: pekarovam@ibp.cz.
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