The impact of oxidative stress and inflammation on RPE degeneration in non-neovascular AMD

• Published in: Progress in retinal and eye research Vol. 60; pp. 201 - 218
• Main Authors: Datta, Sayantan, Cano, Marisol, Ebrahimi, Katayoon, Wang, Lei, Handa, James T.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01-09-2017
• Subjects: Age-related macular degeneration; Complement; Humans; Immunity, Innate - physiology; Inflammation; Macular Degeneration - etiology; Macular Degeneration - physiopathology; Mitochondria - physiology; Mitochondrial dynamics; Nrf2; Oxidative stress; Oxidative Stress - physiology; Phagocytosis - physiology; Retinal pigment epithelium; Retinal Pigment Epithelium - physiopathology; Risk Factors; Oxidative stress; Age-related macular degeneration; Nrf2; Mitochondrial dynamics; Complement; Inflammation; Retinal pigment epithelium
• ISSN: 1350-9462; 1873-1635
• DOI: 10.1016/j.preteyeres.2017.03.002

The retinal pigment epithelium (RPE) is a highly specialized, unique epithelial cell that interacts with photoreceptors on its apical side and with Bruch's membrane and the choriocapillaris on its basal side. Due to vital functions that keep photoreceptors healthy, the RPE is essential for maintaining vision. With aging and the accumulated effects of environmental stresses, the RPE can become dysfunctional and die. This degeneration plays a central role in age-related macular degeneration (AMD) pathobiology, the leading cause of blindness among the elderly in western societies. Oxidative stress and inflammation have both physiological and potentially pathological roles in RPE degeneration. Given the central role of the RPE, this review will focus on the impact of oxidative stress and inflammation on the RPE with AMD pathobiology. Physiological sources of oxidative stress as well as unique sources from photo-oxidative stress, the phagocytosis of photoreceptor outer segments, and modifiable factors such as cigarette smoking and high fat diet ingestion that can convert oxidative stress into a pathological role, and the negative impact of impairing the cytoprotective roles of mitochondrial dynamics and the Nrf2 signaling system on RPE health in AMD will be discussed. Likewise, the response by the innate immune system to an inciting trigger, and the potential role of local RPE production of inflammation, as well as a potential role for damage by inflammation with chronicity if the inciting trigger is not neutralized, will be debated.