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Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy

Nuclear factor, erythroid 2 like 2 (Nrf2), is an oxidative stress induced transcription factor that regulates cytoprotective gene expression. Thus, Nrf2 is essential for cellular redox homeostasis. Loss or dysregulation of Nrf2 expression has been implicated in the pathogenesis of degenerative disea...

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Autores principales: Lovatt, Matthew, Kocaba, Viridiana, Hui Neo, Dawn Jing, Soh, Yu Qiang, Mehta, Jodhbir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578533/
https://www.ncbi.nlm.nih.gov/pubmed/33099215
http://dx.doi.org/10.1016/j.redox.2020.101763
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author Lovatt, Matthew
Kocaba, Viridiana
Hui Neo, Dawn Jing
Soh, Yu Qiang
Mehta, Jodhbir S.
author_facet Lovatt, Matthew
Kocaba, Viridiana
Hui Neo, Dawn Jing
Soh, Yu Qiang
Mehta, Jodhbir S.
author_sort Lovatt, Matthew
collection PubMed
description Nuclear factor, erythroid 2 like 2 (Nrf2), is an oxidative stress induced transcription factor that regulates cytoprotective gene expression. Thus, Nrf2 is essential for cellular redox homeostasis. Loss or dysregulation of Nrf2 expression has been implicated in the pathogenesis of degenerative diseases, including diseases of the cornea. One of the most common diseases of the cornea in which Nrf2 is implicated is Fuchs’ endothelial cornea dystrophy (FECD). FECD is the leading indication for corneal transplantation; and is associated with a loss of corneal endothelial cell (CEC) function. In this review, we propose that Nrf2 is an essential regulator of CEC function. Furthermore, we demonstrate that deficiency of Nrf2 function is a hallmark of FECD. In addition, we advocate that pharmacological targeting of Nrf2 as a possible therapy for FECD.
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spelling pubmed-75785332020-10-23 Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy Lovatt, Matthew Kocaba, Viridiana Hui Neo, Dawn Jing Soh, Yu Qiang Mehta, Jodhbir S. Redox Biol Review Article Nuclear factor, erythroid 2 like 2 (Nrf2), is an oxidative stress induced transcription factor that regulates cytoprotective gene expression. Thus, Nrf2 is essential for cellular redox homeostasis. Loss or dysregulation of Nrf2 expression has been implicated in the pathogenesis of degenerative diseases, including diseases of the cornea. One of the most common diseases of the cornea in which Nrf2 is implicated is Fuchs’ endothelial cornea dystrophy (FECD). FECD is the leading indication for corneal transplantation; and is associated with a loss of corneal endothelial cell (CEC) function. In this review, we propose that Nrf2 is an essential regulator of CEC function. Furthermore, we demonstrate that deficiency of Nrf2 function is a hallmark of FECD. In addition, we advocate that pharmacological targeting of Nrf2 as a possible therapy for FECD. Elsevier 2020-10-16 /pmc/articles/PMC7578533/ /pubmed/33099215 http://dx.doi.org/10.1016/j.redox.2020.101763 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Lovatt, Matthew
Kocaba, Viridiana
Hui Neo, Dawn Jing
Soh, Yu Qiang
Mehta, Jodhbir S.
Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title_full Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title_fullStr Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title_full_unstemmed Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title_short Nrf2: A unifying transcription factor in the pathogenesis of Fuchs’ endothelial corneal dystrophy
title_sort nrf2: a unifying transcription factor in the pathogenesis of fuchs’ endothelial corneal dystrophy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7578533/
https://www.ncbi.nlm.nih.gov/pubmed/33099215
http://dx.doi.org/10.1016/j.redox.2020.101763
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