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Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls

Age-related macular degeneration (AMD) is the primary cause of central blindness among the elderly. AMD is associated with progressive accumulation of lipofuscin granules in retinal pigment epithelium (RPE) cells. Lipofuscin contains bisretinoid fluorophores, which are photosensitizers and are photo...

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Autores principales: Yakovleva, Marina, Dontsov, Alexander, Trofimova, Natalia, Sakina, Natalia, Kononikhin, Alexey, Aybush, Arseny, Gulin, Alexander, Feldman, Tatiana, Ostrovsky, Mikhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745408/
https://www.ncbi.nlm.nih.gov/pubmed/35008647
http://dx.doi.org/10.3390/ijms23010222
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author Yakovleva, Marina
Dontsov, Alexander
Trofimova, Natalia
Sakina, Natalia
Kononikhin, Alexey
Aybush, Arseny
Gulin, Alexander
Feldman, Tatiana
Ostrovsky, Mikhail
author_facet Yakovleva, Marina
Dontsov, Alexander
Trofimova, Natalia
Sakina, Natalia
Kononikhin, Alexey
Aybush, Arseny
Gulin, Alexander
Feldman, Tatiana
Ostrovsky, Mikhail
author_sort Yakovleva, Marina
collection PubMed
description Age-related macular degeneration (AMD) is the primary cause of central blindness among the elderly. AMD is associated with progressive accumulation of lipofuscin granules in retinal pigment epithelium (RPE) cells. Lipofuscin contains bisretinoid fluorophores, which are photosensitizers and are phototoxic to RPE and neuroretinal cells. In the presence of oxygen, bisretinoids are also oxidized, forming various products, consisting primarily of aldehydes and ketones, which are also potentially cytotoxic. In a prior study, we identified that in AMD, bisretinoid oxidation products are increased in RPE lipofuscin granules. The purpose of the present study was to determine if these products were toxic to cellular structures. The physicochemical characteristics of bisretinoid oxidation products in lipofuscin, which were obtained from healthy donor eyes, were studied. Raman spectroscopy and time-of-flight secondary ion mass spectrometry (ToF–SIMS) analysis identified the presence of free-state aldehydes and ketones within the lipofuscin granules. Together, fluorescence spectroscopy, high-performance liquid chromatography, and mass spectrometry revealed that bisretinoid oxidation products have both hydrophilic and amphiphilic properties, allowing their diffusion through lipofuscin granule membrane into the RPE cell cytoplasm. These products contain cytotoxic carbonyls, which can modify cellular proteins and lipids. Therefore, bisretinoid oxidation products are a likely aggravating factor in the pathogenesis of AMD.
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spelling pubmed-87454082022-01-11 Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls Yakovleva, Marina Dontsov, Alexander Trofimova, Natalia Sakina, Natalia Kononikhin, Alexey Aybush, Arseny Gulin, Alexander Feldman, Tatiana Ostrovsky, Mikhail Int J Mol Sci Article Age-related macular degeneration (AMD) is the primary cause of central blindness among the elderly. AMD is associated with progressive accumulation of lipofuscin granules in retinal pigment epithelium (RPE) cells. Lipofuscin contains bisretinoid fluorophores, which are photosensitizers and are phototoxic to RPE and neuroretinal cells. In the presence of oxygen, bisretinoids are also oxidized, forming various products, consisting primarily of aldehydes and ketones, which are also potentially cytotoxic. In a prior study, we identified that in AMD, bisretinoid oxidation products are increased in RPE lipofuscin granules. The purpose of the present study was to determine if these products were toxic to cellular structures. The physicochemical characteristics of bisretinoid oxidation products in lipofuscin, which were obtained from healthy donor eyes, were studied. Raman spectroscopy and time-of-flight secondary ion mass spectrometry (ToF–SIMS) analysis identified the presence of free-state aldehydes and ketones within the lipofuscin granules. Together, fluorescence spectroscopy, high-performance liquid chromatography, and mass spectrometry revealed that bisretinoid oxidation products have both hydrophilic and amphiphilic properties, allowing their diffusion through lipofuscin granule membrane into the RPE cell cytoplasm. These products contain cytotoxic carbonyls, which can modify cellular proteins and lipids. Therefore, bisretinoid oxidation products are a likely aggravating factor in the pathogenesis of AMD. MDPI 2021-12-25 /pmc/articles/PMC8745408/ /pubmed/35008647 http://dx.doi.org/10.3390/ijms23010222 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yakovleva, Marina
Dontsov, Alexander
Trofimova, Natalia
Sakina, Natalia
Kononikhin, Alexey
Aybush, Arseny
Gulin, Alexander
Feldman, Tatiana
Ostrovsky, Mikhail
Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title_full Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title_fullStr Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title_full_unstemmed Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title_short Lipofuscin Granule Bisretinoid Oxidation in the Human Retinal Pigment Epithelium forms Cytotoxic Carbonyls
title_sort lipofuscin granule bisretinoid oxidation in the human retinal pigment epithelium forms cytotoxic carbonyls
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745408/
https://www.ncbi.nlm.nih.gov/pubmed/35008647
http://dx.doi.org/10.3390/ijms23010222
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