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Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina
To discover the mechanisms underlying the progression of diabetic retinopathy (DR), a more comprehensive understanding of the biomolecular processes in individual retinal cells subjected to hyperglycemia is required. Despite extensive studies, the changes in the biochemistry of retinal layers during...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773523/ https://www.ncbi.nlm.nih.gov/pubmed/29348593 http://dx.doi.org/10.1038/s41598-018-19425-8 |
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author | Aboualizadeh, Ebrahim Sorenson, Christine M. Schofield, Alex J. Unger, Miriam Sheibani, Nader Hirschmugl, Carol J. |
author_facet | Aboualizadeh, Ebrahim Sorenson, Christine M. Schofield, Alex J. Unger, Miriam Sheibani, Nader Hirschmugl, Carol J. |
author_sort | Aboualizadeh, Ebrahim |
collection | PubMed |
description | To discover the mechanisms underlying the progression of diabetic retinopathy (DR), a more comprehensive understanding of the biomolecular processes in individual retinal cells subjected to hyperglycemia is required. Despite extensive studies, the changes in the biochemistry of retinal layers during the development of DR are not well known. In this study, we aimed to determine a more detailed understanding of the natural history of DR in Akita/+ (type 1 diabetes model) male mice with different duration of diabetes. Employing label-free spatially resolved Fourier transform infrared (FT-IR) chemical imaging engaged with multivariate analysis enabled us to identify temporal-dependent reproducible biomarkers of the individual retinal layers from mice with 6 weeks,12 weeks, 6 months, and 10 months of age. We report, for the first time, the nature of the biochemical alterations over time in the biochemistry of distinctive retinal layers namely photoreceptor retinal layer (PRL), inner nuclear layer (INL), and plexiform layers (OPL, IPL). Moreover, we present the molecular factors associated with the changes in the protein structure and cellular lipids of retinal layers induced by different duration of diabetes. Our paradigm provides a new conceptual framework for a better understanding of the temporal cellular changes underlying the progression of DR. |
format | Online Article Text |
id | pubmed-5773523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57735232018-01-26 Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina Aboualizadeh, Ebrahim Sorenson, Christine M. Schofield, Alex J. Unger, Miriam Sheibani, Nader Hirschmugl, Carol J. Sci Rep Article To discover the mechanisms underlying the progression of diabetic retinopathy (DR), a more comprehensive understanding of the biomolecular processes in individual retinal cells subjected to hyperglycemia is required. Despite extensive studies, the changes in the biochemistry of retinal layers during the development of DR are not well known. In this study, we aimed to determine a more detailed understanding of the natural history of DR in Akita/+ (type 1 diabetes model) male mice with different duration of diabetes. Employing label-free spatially resolved Fourier transform infrared (FT-IR) chemical imaging engaged with multivariate analysis enabled us to identify temporal-dependent reproducible biomarkers of the individual retinal layers from mice with 6 weeks,12 weeks, 6 months, and 10 months of age. We report, for the first time, the nature of the biochemical alterations over time in the biochemistry of distinctive retinal layers namely photoreceptor retinal layer (PRL), inner nuclear layer (INL), and plexiform layers (OPL, IPL). Moreover, we present the molecular factors associated with the changes in the protein structure and cellular lipids of retinal layers induced by different duration of diabetes. Our paradigm provides a new conceptual framework for a better understanding of the temporal cellular changes underlying the progression of DR. Nature Publishing Group UK 2018-01-18 /pmc/articles/PMC5773523/ /pubmed/29348593 http://dx.doi.org/10.1038/s41598-018-19425-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Aboualizadeh, Ebrahim Sorenson, Christine M. Schofield, Alex J. Unger, Miriam Sheibani, Nader Hirschmugl, Carol J. Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title | Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title_full | Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title_fullStr | Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title_full_unstemmed | Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title_short | Temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
title_sort | temporal diabetes-induced biochemical changes in distinctive layers of mouse retina |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773523/ https://www.ncbi.nlm.nih.gov/pubmed/29348593 http://dx.doi.org/10.1038/s41598-018-19425-8 |
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