Cargando…

Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration

Purpose: The purpose of this study was to examine the effect of plasma rich in growth factors (PRGFs) under blue light conditions in an in vivo model of retinal degeneration. Methods: Male Wistar rats were exposed to dark/blue light conditions for 9 days. On day 7, right eyes were injected with sali...

Descripción completa

Detalles Bibliográficos
Autores principales: Suárez-Barrio, Carlota, del Olmo-Aguado, Susana, García-Pérez, Eva, Artime, Enol, de la Fuente, María, Muruzabal, Francisco, Anitua, Eduardo, Baamonde-Arbaiza, Begoña, Fernández-Vega, Luis, Merayo-Lloves, Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590176/
https://www.ncbi.nlm.nih.gov/pubmed/33050198
http://dx.doi.org/10.3390/ijms21207442
_version_ 1783600747690065920
author Suárez-Barrio, Carlota
del Olmo-Aguado, Susana
García-Pérez, Eva
Artime, Enol
de la Fuente, María
Muruzabal, Francisco
Anitua, Eduardo
Baamonde-Arbaiza, Begoña
Fernández-Vega, Luis
Merayo-Lloves, Jesús
author_facet Suárez-Barrio, Carlota
del Olmo-Aguado, Susana
García-Pérez, Eva
Artime, Enol
de la Fuente, María
Muruzabal, Francisco
Anitua, Eduardo
Baamonde-Arbaiza, Begoña
Fernández-Vega, Luis
Merayo-Lloves, Jesús
author_sort Suárez-Barrio, Carlota
collection PubMed
description Purpose: The purpose of this study was to examine the effect of plasma rich in growth factors (PRGFs) under blue light conditions in an in vivo model of retinal degeneration. Methods: Male Wistar rats were exposed to dark/blue light conditions for 9 days. On day 7, right eyes were injected with saline and left eyes with PRGF. Electroretinography (ERG) and intraocular pressure (IoP) measurements were performed before and after the experiment. After sacrifice, retinal samples were collected. Hematoxylin and eosin staining was performed to analyze the structure of retinal sections. Immunofluorescence for brain-specific homeobox/POU domain protein 3A (Brn3a), choline acetyltransferase (ChAT), rhodopsin, heme oxygenase-1 (HO-1), and glial fibrillary acidic protein (GFAP) was performed to study the retinal conditions. Results: Retinal signaling measured by ERG was reduced by blue light and recovered with PRGF; however, IoP measurements did not show significant differences among treatments. Blue light reduced the expression for Brn3a, ChAT, and rhodopsin. Treatment with PRGF showed a recovery in their expressions. HO-1 and GFAP results showed that blue light increased their expression but the use of PRGF reduced the effect of light. Conclusions: Blue light causes retinal degeneration. PRGF mitigated the injury, restoring the functionality of these cells and maintaining the tissue integrity.
format Online
Article
Text
id pubmed-7590176
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-75901762020-10-29 Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration Suárez-Barrio, Carlota del Olmo-Aguado, Susana García-Pérez, Eva Artime, Enol de la Fuente, María Muruzabal, Francisco Anitua, Eduardo Baamonde-Arbaiza, Begoña Fernández-Vega, Luis Merayo-Lloves, Jesús Int J Mol Sci Article Purpose: The purpose of this study was to examine the effect of plasma rich in growth factors (PRGFs) under blue light conditions in an in vivo model of retinal degeneration. Methods: Male Wistar rats were exposed to dark/blue light conditions for 9 days. On day 7, right eyes were injected with saline and left eyes with PRGF. Electroretinography (ERG) and intraocular pressure (IoP) measurements were performed before and after the experiment. After sacrifice, retinal samples were collected. Hematoxylin and eosin staining was performed to analyze the structure of retinal sections. Immunofluorescence for brain-specific homeobox/POU domain protein 3A (Brn3a), choline acetyltransferase (ChAT), rhodopsin, heme oxygenase-1 (HO-1), and glial fibrillary acidic protein (GFAP) was performed to study the retinal conditions. Results: Retinal signaling measured by ERG was reduced by blue light and recovered with PRGF; however, IoP measurements did not show significant differences among treatments. Blue light reduced the expression for Brn3a, ChAT, and rhodopsin. Treatment with PRGF showed a recovery in their expressions. HO-1 and GFAP results showed that blue light increased their expression but the use of PRGF reduced the effect of light. Conclusions: Blue light causes retinal degeneration. PRGF mitigated the injury, restoring the functionality of these cells and maintaining the tissue integrity. MDPI 2020-10-09 /pmc/articles/PMC7590176/ /pubmed/33050198 http://dx.doi.org/10.3390/ijms21207442 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Suárez-Barrio, Carlota
del Olmo-Aguado, Susana
García-Pérez, Eva
Artime, Enol
de la Fuente, María
Muruzabal, Francisco
Anitua, Eduardo
Baamonde-Arbaiza, Begoña
Fernández-Vega, Luis
Merayo-Lloves, Jesús
Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title_full Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title_fullStr Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title_full_unstemmed Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title_short Plasma Rich in Growth Factors Enhances Cell Survival after in Situ Retinal Degeneration
title_sort plasma rich in growth factors enhances cell survival after in situ retinal degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7590176/
https://www.ncbi.nlm.nih.gov/pubmed/33050198
http://dx.doi.org/10.3390/ijms21207442
work_keys_str_mv AT suarezbarriocarlota plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT delolmoaguadosusana plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT garciaperezeva plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT artimeenol plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT delafuentemaria plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT muruzabalfrancisco plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT anituaeduardo plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT baamondearbaizabegona plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT fernandezvegaluis plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration
AT merayollovesjesus plasmarichingrowthfactorsenhancescellsurvivalafterinsituretinaldegeneration