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The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model

The purpose was to study the anti-angiogenic effect of adipose-derived mesenchymal stem/stromal cells (ADMSCs) on experimentally induced corneal injuries. Corneal neovascularization (NV) was induced by incising and subsequently suturing the corneal surface in 32 New Zealand rabbits. Following suturi...

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Autores principales: Pirounides, Demetrios, Komnenou, Anastasia, Papaioannou, Nikolaos, Gounari, Eleni, Stylianaki, Ioanna, Alexandridis, Alexandros, Chranioti, Angeliki, Kofidou, Evangelia, Koliakos, Georgios, Karampatakis, Vasileios
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical Hypothesis, Discovery & Innovation Ophthalmology 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134242/
https://www.ncbi.nlm.nih.gov/pubmed/32490014
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author Pirounides, Demetrios
Komnenou, Anastasia
Papaioannou, Nikolaos
Gounari, Eleni
Stylianaki, Ioanna
Alexandridis, Alexandros
Chranioti, Angeliki
Kofidou, Evangelia
Koliakos, Georgios
Karampatakis, Vasileios
author_facet Pirounides, Demetrios
Komnenou, Anastasia
Papaioannou, Nikolaos
Gounari, Eleni
Stylianaki, Ioanna
Alexandridis, Alexandros
Chranioti, Angeliki
Kofidou, Evangelia
Koliakos, Georgios
Karampatakis, Vasileios
author_sort Pirounides, Demetrios
collection PubMed
description The purpose was to study the anti-angiogenic effect of adipose-derived mesenchymal stem/stromal cells (ADMSCs) on experimentally induced corneal injuries. Corneal neovascularization (NV) was induced by incising and subsequently suturing the corneal surface in 32 New Zealand rabbits. Following suturing, the rabbits were randomly allocated into 2 groups, and received either phosphate-buffered saline (PBS) (control) or ADMSCs, both administered via three different routes. Digital images of the cornea were obtained two weeks post-incision to measure the area of neovascularized cornea. Tumor necrosis factor (TNF) was immunohistochemically assessed in the both groups. The corneal tissue was evaluated for vascular endothelial growth factor (VEGF). The extent of corneal NV in all eyes was assessed photographically by an independent observer. Fourteen days after the incisions, the degree of corneal NV was substantially decreased in the ADMSC-treated group (1.87 ± 0.9 mm(2), 1.4 % ± 0.67 % of corneal surface) compared to the control and PBS-treated group (4.66 ± 1.74 mm(2), 3.51 % ± 1.31 %, p < 0.001). ADMSCs significantly decreased injury-induced corneal NV in New Zealand rabbits two weeks post-treatment. This strategy has potential for use in the control of corneal NV in vivo.
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spelling pubmed-71342422020-06-01 The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model Pirounides, Demetrios Komnenou, Anastasia Papaioannou, Nikolaos Gounari, Eleni Stylianaki, Ioanna Alexandridis, Alexandros Chranioti, Angeliki Kofidou, Evangelia Koliakos, Georgios Karampatakis, Vasileios Med Hypothesis Discov Innov Ophthalmol Original Article The purpose was to study the anti-angiogenic effect of adipose-derived mesenchymal stem/stromal cells (ADMSCs) on experimentally induced corneal injuries. Corneal neovascularization (NV) was induced by incising and subsequently suturing the corneal surface in 32 New Zealand rabbits. Following suturing, the rabbits were randomly allocated into 2 groups, and received either phosphate-buffered saline (PBS) (control) or ADMSCs, both administered via three different routes. Digital images of the cornea were obtained two weeks post-incision to measure the area of neovascularized cornea. Tumor necrosis factor (TNF) was immunohistochemically assessed in the both groups. The corneal tissue was evaluated for vascular endothelial growth factor (VEGF). The extent of corneal NV in all eyes was assessed photographically by an independent observer. Fourteen days after the incisions, the degree of corneal NV was substantially decreased in the ADMSC-treated group (1.87 ± 0.9 mm(2), 1.4 % ± 0.67 % of corneal surface) compared to the control and PBS-treated group (4.66 ± 1.74 mm(2), 3.51 % ± 1.31 %, p < 0.001). ADMSCs significantly decreased injury-induced corneal NV in New Zealand rabbits two weeks post-treatment. This strategy has potential for use in the control of corneal NV in vivo. Medical Hypothesis, Discovery & Innovation Ophthalmology 2020 2020-03-12 /pmc/articles/PMC7134242/ /pubmed/32490014 Text en Copyright © 2020, Author(s) This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial 4.0 International License (http://creativecommons.org/licenses/by/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
spellingShingle Original Article
Pirounides, Demetrios
Komnenou, Anastasia
Papaioannou, Nikolaos
Gounari, Eleni
Stylianaki, Ioanna
Alexandridis, Alexandros
Chranioti, Angeliki
Kofidou, Evangelia
Koliakos, Georgios
Karampatakis, Vasileios
The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title_full The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title_fullStr The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title_full_unstemmed The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title_short The Antiangiogenic Properties of Adipose-Derived Mesenchymal Stem/Stromal Cells in Corneal Neovascularization in a Rabbit Model
title_sort antiangiogenic properties of adipose-derived mesenchymal stem/stromal cells in corneal neovascularization in a rabbit model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7134242/
https://www.ncbi.nlm.nih.gov/pubmed/32490014
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