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Updated: Apr 1, 2026

A Protocol to Evaluate and Quantify Retinal Pigmented Epithelium Pathologies in Mouse Models of Age-Related Macular Degeneration
Published on: March 10, 2023
Biology of p62/sequestosome-1 in Age-Related Macular Degeneration (AMD)
Lei Wang1, Katayoon B Ebrahimi2, Michelle Chyn3
1Wilmer Eye Institute, Johns Hopkins School of Medicine, 400 N Broadway, Rm 3001-D, the Smith Building, 21287, Baltimore, MD, USA. leiwang.011@gmail.com.
Abstract:
p62/sequestosome-1 is a multidimensional protein that interacts with many signaling factors, and regulates a variety of cellular functions including inflammation, apoptosis, and autophagy. Our previous work has revealed in the retinal pigment epithelium (RPE) that p62 promotes autophagy and simultaneously enhances an Nrf2-mediated antioxidant response to protect against acute oxidative stress. Several recent studies demonstrated that p62 contributes to NFkB mediated inflammation and inflammasome activation under certain circumstances, raising the question of whether p62 protects against or contributes to tissue injury. Herein, we will review the general characteristics of p62, focusing on its pro- and anti-cell survival roles within different physiological/pathological contexts, and discuss the potential of p62 as a therapeutic target for AMD.

