NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration

Age-related macular degeneration (AMD) is the leading cause of legal blindness in the elderly in industrialized countries. AMD is a multifactorial disease influenced by both genetic and environmental risk factors. Progression of AMD is characterized by an increase in the number and size of drusen, e...

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Main Authors: Jiangyuan Gao, Ruozhou Tom Liu, Sijia Cao, Jing Z. Cui, Aikun Wang, Eleanor To, Joanne A. Matsubara
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2015/690243
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author Jiangyuan Gao
Ruozhou Tom Liu
Sijia Cao
Jing Z. Cui
Aikun Wang
Eleanor To
Joanne A. Matsubara
author_facet Jiangyuan Gao
Ruozhou Tom Liu
Sijia Cao
Jing Z. Cui
Aikun Wang
Eleanor To
Joanne A. Matsubara
author_sort Jiangyuan Gao
collection DOAJ
description Age-related macular degeneration (AMD) is the leading cause of legal blindness in the elderly in industrialized countries. AMD is a multifactorial disease influenced by both genetic and environmental risk factors. Progression of AMD is characterized by an increase in the number and size of drusen, extracellular deposits, which accumulate between the retinal pigment epithelium (RPE) and Bruch’s membrane (BM) in outer retina. The major pathways associated with its pathogenesis include oxidative stress and inflammation in the early stages of AMD. Little is known about the interactions among these mechanisms that drive the transition from early to late stages of AMD, such as geographic atrophy (GA) or choroidal neovascularization (CNV). As part of the innate immune system, inflammasome activation has been identified in RPE cells and proposed to be a causal factor for RPE dysfunction and degeneration. Here, we will first review the classic model of inflammasome activation, then discuss the potentials of AMD-related factors to activate the inflammasome in both nonocular immune cells and RPE cells, and finally introduce several novel mechanisms for regulating the inflammasome activity.
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institution Kabale University
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publishDate 2015-01-01
publisher Wiley
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series Mediators of Inflammation
spelling doaj-art-0d2d3063c364495e8f69ca9beeda1bf52025-02-03T01:12:04ZengWileyMediators of Inflammation0962-93511466-18612015-01-01201510.1155/2015/690243690243NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular DegenerationJiangyuan Gao0Ruozhou Tom Liu1Sijia Cao2Jing Z. Cui3Aikun Wang4Eleanor To5Joanne A. Matsubara6Department of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaDepartment of Ophthalmology and Visual Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, V5Z 3N9, CanadaAge-related macular degeneration (AMD) is the leading cause of legal blindness in the elderly in industrialized countries. AMD is a multifactorial disease influenced by both genetic and environmental risk factors. Progression of AMD is characterized by an increase in the number and size of drusen, extracellular deposits, which accumulate between the retinal pigment epithelium (RPE) and Bruch’s membrane (BM) in outer retina. The major pathways associated with its pathogenesis include oxidative stress and inflammation in the early stages of AMD. Little is known about the interactions among these mechanisms that drive the transition from early to late stages of AMD, such as geographic atrophy (GA) or choroidal neovascularization (CNV). As part of the innate immune system, inflammasome activation has been identified in RPE cells and proposed to be a causal factor for RPE dysfunction and degeneration. Here, we will first review the classic model of inflammasome activation, then discuss the potentials of AMD-related factors to activate the inflammasome in both nonocular immune cells and RPE cells, and finally introduce several novel mechanisms for regulating the inflammasome activity.http://dx.doi.org/10.1155/2015/690243
spellingShingle Jiangyuan Gao
Ruozhou Tom Liu
Sijia Cao
Jing Z. Cui
Aikun Wang
Eleanor To
Joanne A. Matsubara
NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
Mediators of Inflammation
title NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
title_full NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
title_fullStr NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
title_full_unstemmed NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
title_short NLRP3 Inflammasome: Activation and Regulation in Age-Related Macular Degeneration
title_sort nlrp3 inflammasome activation and regulation in age related macular degeneration
url http://dx.doi.org/10.1155/2015/690243
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