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SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells

PURPOSE: Corneal endothelial cells are rich in mitochondria, a potential source of reactive oxygen species (ROS). ROS have been implicated in endothelial cell loss during aging or in endothelial dystrophies. In this study we examined the anti-oxidative role of mitochondrial superoxide dismutase (SOD...

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Autores principales: Liu, Cailing, Ogando, Diego, Bonanno, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185022/
https://www.ncbi.nlm.nih.gov/pubmed/21976958
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author Liu, Cailing
Ogando, Diego
Bonanno, Joseph A.
author_facet Liu, Cailing
Ogando, Diego
Bonanno, Joseph A.
author_sort Liu, Cailing
collection PubMed
description PURPOSE: Corneal endothelial cells are rich in mitochondria, a potential source of reactive oxygen species (ROS). ROS have been implicated in endothelial cell loss during aging or in endothelial dystrophies. In this study we examined the anti-oxidative role of mitochondrial superoxide dismutase (SOD2) in corneal endothelial cells. METHODS: SOD2 expression was examined by RT–PCR and western blot analysis in fresh rabbit corneal endothelium (RCE) and cell cultures. SOD2 activity, total reactive oxygen species (ROS), mitochondrial ROS, mitochondrial membrane potential (MMP), and apoptotic levels were examined in untreated, SOD2 siRNA and viral vector shRNA treated RCE cells. Scrambled siRNA and shRNA sequence targeting non-mammalian genes were used as controls. RESULTS: SOD2 is expressed in both fresh and cultured rabbit corneal endothelium. SOD2 expression was reduced by ~80%–90% in cultured RCE using either siRNA or shRNA approaches. SOD2 activity was decreased by ~70%–80% for both approaches. Total cell ROS was significantly increased in shSOD2 lentivirus treated cells (9%±6%) relative to control transduction (0.4%±0.1%). MitoSOX™ staining for mitochondrial ROS in siSOD2 treated RCE cells was dramatically increased. Two minutes of UV irradiation increased total ROS levels by 15%, whereas in shSOD2 treated cells UV induced ROS was increased 29%±5% (p<0.05). MMP was reduced in shSOD2 viral treated cells by 66%±3%, significantly greater than in control transduced cells (15%±8%, p<0.05). Apoptosis increased by 1.5 fold in shSOD2 virus treated samples compared with scrambled virus and untreated cells. CONCLUSIONS: SOD2 is expressed in both fresh and cultured rabbit corneal endothelium. siRNA and shRNA approaches are able to efficiently knockdown SOD2 expression and reduce enzyme activity in RCE cells. Decreased SOD2 activity causes elevated ROS production, mitochondrial membrane potential loss and early cell apoptosis. These results indicate that SOD2 is a significant anti-oxidative enzyme in RCE cells.
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spelling pubmed-31850222011-10-04 SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells Liu, Cailing Ogando, Diego Bonanno, Joseph A. Mol Vis Research Article PURPOSE: Corneal endothelial cells are rich in mitochondria, a potential source of reactive oxygen species (ROS). ROS have been implicated in endothelial cell loss during aging or in endothelial dystrophies. In this study we examined the anti-oxidative role of mitochondrial superoxide dismutase (SOD2) in corneal endothelial cells. METHODS: SOD2 expression was examined by RT–PCR and western blot analysis in fresh rabbit corneal endothelium (RCE) and cell cultures. SOD2 activity, total reactive oxygen species (ROS), mitochondrial ROS, mitochondrial membrane potential (MMP), and apoptotic levels were examined in untreated, SOD2 siRNA and viral vector shRNA treated RCE cells. Scrambled siRNA and shRNA sequence targeting non-mammalian genes were used as controls. RESULTS: SOD2 is expressed in both fresh and cultured rabbit corneal endothelium. SOD2 expression was reduced by ~80%–90% in cultured RCE using either siRNA or shRNA approaches. SOD2 activity was decreased by ~70%–80% for both approaches. Total cell ROS was significantly increased in shSOD2 lentivirus treated cells (9%±6%) relative to control transduction (0.4%±0.1%). MitoSOX™ staining for mitochondrial ROS in siSOD2 treated RCE cells was dramatically increased. Two minutes of UV irradiation increased total ROS levels by 15%, whereas in shSOD2 treated cells UV induced ROS was increased 29%±5% (p<0.05). MMP was reduced in shSOD2 viral treated cells by 66%±3%, significantly greater than in control transduced cells (15%±8%, p<0.05). Apoptosis increased by 1.5 fold in shSOD2 virus treated samples compared with scrambled virus and untreated cells. CONCLUSIONS: SOD2 is expressed in both fresh and cultured rabbit corneal endothelium. siRNA and shRNA approaches are able to efficiently knockdown SOD2 expression and reduce enzyme activity in RCE cells. Decreased SOD2 activity causes elevated ROS production, mitochondrial membrane potential loss and early cell apoptosis. These results indicate that SOD2 is a significant anti-oxidative enzyme in RCE cells. Molecular Vision 2011-09-24 /pmc/articles/PMC3185022/ /pubmed/21976958 Text en Copyright © 2011 Molecular Vision. http://creativecommons.org/licenses/by/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.
spellingShingle Research Article
Liu, Cailing
Ogando, Diego
Bonanno, Joseph A.
SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title_full SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title_fullStr SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title_full_unstemmed SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title_short SOD2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
title_sort sod2 contributes to anti-oxidative capacity in rabbit corneal endothelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185022/
https://www.ncbi.nlm.nih.gov/pubmed/21976958
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