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Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation

PURPOSE: To evaluate whether anti-vascular endothelial growth factor (VEGF) neutralizing antibodies injected in the vitreous of rat eyes influence retinal microglia and macrophage activation. To dissociate the effect of anti-VEGF on microglia and macrophages subsequent to its antiangiogenic effect,...

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Autores principales: Couturier, Aude, Bousquet, Elodie, Zhao, Min, Naud, Marie-Christine, Klein, Christophe, Jonet, Laurent, Tadayoni, Ramin, de Kozak, Yvonne, Behar-Cohen, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067232/
https://www.ncbi.nlm.nih.gov/pubmed/24966662
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author Couturier, Aude
Bousquet, Elodie
Zhao, Min
Naud, Marie-Christine
Klein, Christophe
Jonet, Laurent
Tadayoni, Ramin
de Kozak, Yvonne
Behar-Cohen, F.
author_facet Couturier, Aude
Bousquet, Elodie
Zhao, Min
Naud, Marie-Christine
Klein, Christophe
Jonet, Laurent
Tadayoni, Ramin
de Kozak, Yvonne
Behar-Cohen, F.
author_sort Couturier, Aude
collection PubMed
description PURPOSE: To evaluate whether anti-vascular endothelial growth factor (VEGF) neutralizing antibodies injected in the vitreous of rat eyes influence retinal microglia and macrophage activation. To dissociate the effect of anti-VEGF on microglia and macrophages subsequent to its antiangiogenic effect, we chose a model of acute intraocular inflammation. METHODS: Lewis rats were challenged with systemic lipopolysaccharide (LPS) injection and concomitantly received 5 µl of rat anti-VEGF-neutralizing antibody (1.5 mg/ml) in the vitreous. Rat immunoglobulin G (IgG) isotype was used as the control. The effect of anti-VEGF was evaluated at 24 and 48 h clinically (uveitis scores), biologically (cytokine multiplex analysis in ocular media), and histologically (inflammatory cell counts on eye sections). Microglia and macrophages were immunodetected with ionized calcium-binding adaptor molecule 1 (IBA1) staining and counted based on their differential shapes (round amoeboid or ramified dendritiform) on sections and flatmounted retinas using confocal imaging and automatic quantification. Activation of microglia was also evaluated with inducible nitric oxide synthase (iNOS) and IBA1 coimmunostaining. Coimmunolocalization of VEGF receptor 1 and 2 (VEGF-R1 and R2) with IBA1 was performed on eye sections with or without anti-VEGF treatment. RESULTS: Neutralizing rat anti-VEGF antibodies significantly decreased ocular VEGF levels but did not decrease the endotoxin-induced uveitis (EIU) clinical score or the number of infiltrating cells and cytokines in ocular media (interleukin [IL]-1β, IL-6, tumor necrosis factor [TNF]-α, and monocyte chemoattractant protein [MCP]-1). Eyes treated with anti-VEGF showed a significantly decreased number of activated microglia and macrophages in the retina and the choroid and decreased iNOS-positive microglia. IBA1-positive cells expressed VEGF-R1 and R2 in the inflamed retina. CONCLUSIONS: Microglia and macrophages expressed VEGF receptors, and intravitreous anti-VEGF influenced the microglia and macrophage activation state. Taking into account that anti-VEGF drugs are repeatedly injected in the vitreous of patients with retinal diseases, part of their effects could result from unsuspected modulation of the microglia activation state. This should be further studied in other ocular pathogenic conditions and human pathology.
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spelling pubmed-40672322014-06-25 Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation Couturier, Aude Bousquet, Elodie Zhao, Min Naud, Marie-Christine Klein, Christophe Jonet, Laurent Tadayoni, Ramin de Kozak, Yvonne Behar-Cohen, F. Mol Vis Research Article PURPOSE: To evaluate whether anti-vascular endothelial growth factor (VEGF) neutralizing antibodies injected in the vitreous of rat eyes influence retinal microglia and macrophage activation. To dissociate the effect of anti-VEGF on microglia and macrophages subsequent to its antiangiogenic effect, we chose a model of acute intraocular inflammation. METHODS: Lewis rats were challenged with systemic lipopolysaccharide (LPS) injection and concomitantly received 5 µl of rat anti-VEGF-neutralizing antibody (1.5 mg/ml) in the vitreous. Rat immunoglobulin G (IgG) isotype was used as the control. The effect of anti-VEGF was evaluated at 24 and 48 h clinically (uveitis scores), biologically (cytokine multiplex analysis in ocular media), and histologically (inflammatory cell counts on eye sections). Microglia and macrophages were immunodetected with ionized calcium-binding adaptor molecule 1 (IBA1) staining and counted based on their differential shapes (round amoeboid or ramified dendritiform) on sections and flatmounted retinas using confocal imaging and automatic quantification. Activation of microglia was also evaluated with inducible nitric oxide synthase (iNOS) and IBA1 coimmunostaining. Coimmunolocalization of VEGF receptor 1 and 2 (VEGF-R1 and R2) with IBA1 was performed on eye sections with or without anti-VEGF treatment. RESULTS: Neutralizing rat anti-VEGF antibodies significantly decreased ocular VEGF levels but did not decrease the endotoxin-induced uveitis (EIU) clinical score or the number of infiltrating cells and cytokines in ocular media (interleukin [IL]-1β, IL-6, tumor necrosis factor [TNF]-α, and monocyte chemoattractant protein [MCP]-1). Eyes treated with anti-VEGF showed a significantly decreased number of activated microglia and macrophages in the retina and the choroid and decreased iNOS-positive microglia. IBA1-positive cells expressed VEGF-R1 and R2 in the inflamed retina. CONCLUSIONS: Microglia and macrophages expressed VEGF receptors, and intravitreous anti-VEGF influenced the microglia and macrophage activation state. Taking into account that anti-VEGF drugs are repeatedly injected in the vitreous of patients with retinal diseases, part of their effects could result from unsuspected modulation of the microglia activation state. This should be further studied in other ocular pathogenic conditions and human pathology. Molecular Vision 2014-06-23 /pmc/articles/PMC4067232/ /pubmed/24966662 Text en Copyright © 2014 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited, used for non-commercial purposes, and is not altered or transformed.
spellingShingle Research Article
Couturier, Aude
Bousquet, Elodie
Zhao, Min
Naud, Marie-Christine
Klein, Christophe
Jonet, Laurent
Tadayoni, Ramin
de Kozak, Yvonne
Behar-Cohen, F.
Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title_full Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title_fullStr Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title_full_unstemmed Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title_short Anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
title_sort anti-vascular endothelial growth factor acts on retinal microglia/macrophage activation in a rat model of ocular inflammation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067232/
https://www.ncbi.nlm.nih.gov/pubmed/24966662
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