Dontsov, A.; Ostrovsky, M. Retinal Pigment Epithelium Pigment Granules: Norms, Age Relations and Pathology. Int. J. Mol. Sci.2024, 25, 3609.
Dontsov, A.; Ostrovsky, M. Retinal Pigment Epithelium Pigment Granules: Norms, Age Relations and Pathology. Int. J. Mol. Sci. 2024, 25, 3609.
Dontsov, A.; Ostrovsky, M. Retinal Pigment Epithelium Pigment Granules: Norms, Age Relations and Pathology. Int. J. Mol. Sci.2024, 25, 3609.
Dontsov, A.; Ostrovsky, M. Retinal Pigment Epithelium Pigment Granules: Norms, Age Relations and Pathology. Int. J. Mol. Sci. 2024, 25, 3609.
Abstract
The retinal pigment epithelium (RPE), which ensures the normal functioning of the neural retina, is a pigmented single-cell layer that separates the retina from the Bruch's membrane and the choroid. There are three main types of pigment granules in the RPE cells of the human eye: lipofuscin granules (LG) containing the fluorescent “age pigment” lipofuscin, melanoprotein granules (melanosomes, melanolysosomes) containing the screening pigment melanin and complex melanolipofuscin granules (MLG) containing simultaneously both types of pigments - melanin and lipofuscin. This review examines the functional role of pigment granules in the aging process and in the development of oxidative stress and associated pathologies in RPE cells. The focus is on the process of light-induced oxidative degradation of pigment granules caused by reactive oxygen species. The reasons leading to increased oxidative stress in RPE cells as a result of oxidative degradation of pigment granules are considered. A mechanism has been proposed to explain the phenomenon of age-related decline in melanin content in RPE cells. The essence of the mechanism is that when the lipofuscin part of the melanolipofuscin granule is exposed to light, reactive oxygen species are formed, which destroy its melanin part. As more melanolipofuscin granules are formed with age and the development of degenerative diseases, the melanin in pigmented epithelial cells ultimately disappears.
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