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Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion

Aflibercept is a frequently used inhibitor of vascular endothelial growth factor (VEGF) in the treatment of macular edema following central retinal vein occlusion (CRVO). Retinal proteome changes following aflibercept intervention in CRVO remain largely unstudied. Studying proteomic changes of aflib...

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Autores principales: Cehofski, Lasse Jørgensen, Kruse, Anders, Alsing, Alexander Nørgaard, Sejergaard, Benn Falch, Nielsen, Jonas Ellegaard, Schlosser, Anders, Sorensen, Grith Lykke, Grauslund, Jakob, Honoré, Bent, Vorum, Henrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182497/
https://www.ncbi.nlm.nih.gov/pubmed/35684299
http://dx.doi.org/10.3390/molecules27113360
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author Cehofski, Lasse Jørgensen
Kruse, Anders
Alsing, Alexander Nørgaard
Sejergaard, Benn Falch
Nielsen, Jonas Ellegaard
Schlosser, Anders
Sorensen, Grith Lykke
Grauslund, Jakob
Honoré, Bent
Vorum, Henrik
author_facet Cehofski, Lasse Jørgensen
Kruse, Anders
Alsing, Alexander Nørgaard
Sejergaard, Benn Falch
Nielsen, Jonas Ellegaard
Schlosser, Anders
Sorensen, Grith Lykke
Grauslund, Jakob
Honoré, Bent
Vorum, Henrik
author_sort Cehofski, Lasse Jørgensen
collection PubMed
description Aflibercept is a frequently used inhibitor of vascular endothelial growth factor (VEGF) in the treatment of macular edema following central retinal vein occlusion (CRVO). Retinal proteome changes following aflibercept intervention in CRVO remain largely unstudied. Studying proteomic changes of aflibercept intervention may generate a better understanding of mechanisms of action and uncover aspects related to the safety profile. In 10 Danish Landrace pigs, CRVO was induced in both eyes with an argon laser. Right eyes were treated with intravitreal aflibercept while left control eyes received isotonic saline water. Retinal samples were collected 15 days after induced CRVO. Proteomic analysis by tandem mass tag-based mass spectrometry identified a total of 21 proteins that were changed in content following aflibercept intervention. In retinas treated with aflibercept, high levels of aflibercept components were reached, including the VEGF receptor-1 and VEGF receptor-2 domains. Fold changes in the additional proteins ranged between 0.70 and 1.19. Aflibercept intervention resulted in a downregulation of pigment epithelium-derived factor (PEDF) (fold change = 0.84) and endoplasmin (fold change = 0.91). The changes were slight and could thereby not be confirmed with less precise immunohistochemistry and Western blotting. Our data suggest that aflibercept had a narrow mechanism of action in the CRVO model. This may be an important observation in cases when macular edema secondary to CRVO is resistant to aflibercept intervention.
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spelling pubmed-91824972022-06-10 Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion Cehofski, Lasse Jørgensen Kruse, Anders Alsing, Alexander Nørgaard Sejergaard, Benn Falch Nielsen, Jonas Ellegaard Schlosser, Anders Sorensen, Grith Lykke Grauslund, Jakob Honoré, Bent Vorum, Henrik Molecules Article Aflibercept is a frequently used inhibitor of vascular endothelial growth factor (VEGF) in the treatment of macular edema following central retinal vein occlusion (CRVO). Retinal proteome changes following aflibercept intervention in CRVO remain largely unstudied. Studying proteomic changes of aflibercept intervention may generate a better understanding of mechanisms of action and uncover aspects related to the safety profile. In 10 Danish Landrace pigs, CRVO was induced in both eyes with an argon laser. Right eyes were treated with intravitreal aflibercept while left control eyes received isotonic saline water. Retinal samples were collected 15 days after induced CRVO. Proteomic analysis by tandem mass tag-based mass spectrometry identified a total of 21 proteins that were changed in content following aflibercept intervention. In retinas treated with aflibercept, high levels of aflibercept components were reached, including the VEGF receptor-1 and VEGF receptor-2 domains. Fold changes in the additional proteins ranged between 0.70 and 1.19. Aflibercept intervention resulted in a downregulation of pigment epithelium-derived factor (PEDF) (fold change = 0.84) and endoplasmin (fold change = 0.91). The changes were slight and could thereby not be confirmed with less precise immunohistochemistry and Western blotting. Our data suggest that aflibercept had a narrow mechanism of action in the CRVO model. This may be an important observation in cases when macular edema secondary to CRVO is resistant to aflibercept intervention. MDPI 2022-05-24 /pmc/articles/PMC9182497/ /pubmed/35684299 http://dx.doi.org/10.3390/molecules27113360 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cehofski, Lasse Jørgensen
Kruse, Anders
Alsing, Alexander Nørgaard
Sejergaard, Benn Falch
Nielsen, Jonas Ellegaard
Schlosser, Anders
Sorensen, Grith Lykke
Grauslund, Jakob
Honoré, Bent
Vorum, Henrik
Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title_full Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title_fullStr Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title_full_unstemmed Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title_short Proteome Analysis of Aflibercept Intervention in Experimental Central Retinal Vein Occlusion
title_sort proteome analysis of aflibercept intervention in experimental central retinal vein occlusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182497/
https://www.ncbi.nlm.nih.gov/pubmed/35684299
http://dx.doi.org/10.3390/molecules27113360
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