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Aldo-Keto Reductases in the Eye
Aldose reductase (AKR1B1) is an NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Accelerated glucose metabolism through this pathway has been implicated in diabetic cataract and retinopathy. Some human tissues contain AKR1B1 as well as AKR1B10, a clos...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902055/ https://www.ncbi.nlm.nih.gov/pubmed/20628518 http://dx.doi.org/10.1155/2010/521204 |
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author | Huang, Shun Ping Palla, Suryanarayana Ruzycki, Philip Varma, Ross Arjun Harter, Theresa Reddy, G. Bhanuprakesh Petrash, J. Mark |
author_facet | Huang, Shun Ping Palla, Suryanarayana Ruzycki, Philip Varma, Ross Arjun Harter, Theresa Reddy, G. Bhanuprakesh Petrash, J. Mark |
author_sort | Huang, Shun Ping |
collection | PubMed |
description | Aldose reductase (AKR1B1) is an NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Accelerated glucose metabolism through this pathway has been implicated in diabetic cataract and retinopathy. Some human tissues contain AKR1B1 as well as AKR1B10, a closely related member of the aldo-keto reductase gene superfamily. This opens the possibility that AKR1B10 may also contribute to diabetic complications. The goal of the current study was to characterize the expression profiles of AKR1B1 and AKR1B10 in the human eye. Using quantitative reverse transcriptase-PCR and immunohistochemical staining, we observed expression of both AKR genes in cornea, iris, ciliary body, lens, and retina. Expression of AKR1B1 was the highest in lens and retina, whereas AKR1B10 was the highest in cornea. Lenses from transgenic mice designed for overexpression of AKR1B10 were not significantly different from nontransgenic controls, although a significant number developed a focal defect in the anterior lens epithelium following 6 months of experimentally induced diabetes. However, lenses from AKR1B10 mice remained largely transparent following longterm diabetes. These results indicate that AKR1B1 and AKR1B10 may have different functional properties in the lens and suggest that AKR1B10 does not contribute to the pathogenesis of diabetic cataract in humans. |
format | Text |
id | pubmed-2902055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-29020552010-07-13 Aldo-Keto Reductases in the Eye Huang, Shun Ping Palla, Suryanarayana Ruzycki, Philip Varma, Ross Arjun Harter, Theresa Reddy, G. Bhanuprakesh Petrash, J. Mark J Ophthalmol Research Article Aldose reductase (AKR1B1) is an NADPH-dependent aldo-keto reductase best known as the rate-limiting enzyme of the polyol pathway. Accelerated glucose metabolism through this pathway has been implicated in diabetic cataract and retinopathy. Some human tissues contain AKR1B1 as well as AKR1B10, a closely related member of the aldo-keto reductase gene superfamily. This opens the possibility that AKR1B10 may also contribute to diabetic complications. The goal of the current study was to characterize the expression profiles of AKR1B1 and AKR1B10 in the human eye. Using quantitative reverse transcriptase-PCR and immunohistochemical staining, we observed expression of both AKR genes in cornea, iris, ciliary body, lens, and retina. Expression of AKR1B1 was the highest in lens and retina, whereas AKR1B10 was the highest in cornea. Lenses from transgenic mice designed for overexpression of AKR1B10 were not significantly different from nontransgenic controls, although a significant number developed a focal defect in the anterior lens epithelium following 6 months of experimentally induced diabetes. However, lenses from AKR1B10 mice remained largely transparent following longterm diabetes. These results indicate that AKR1B1 and AKR1B10 may have different functional properties in the lens and suggest that AKR1B10 does not contribute to the pathogenesis of diabetic cataract in humans. Hindawi Publishing Corporation 2010 2010-06-13 /pmc/articles/PMC2902055/ /pubmed/20628518 http://dx.doi.org/10.1155/2010/521204 Text en Copyright © 2010 Shun Ping Huang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Huang, Shun Ping Palla, Suryanarayana Ruzycki, Philip Varma, Ross Arjun Harter, Theresa Reddy, G. Bhanuprakesh Petrash, J. Mark Aldo-Keto Reductases in the Eye |
title | Aldo-Keto Reductases in the Eye |
title_full | Aldo-Keto Reductases in the Eye |
title_fullStr | Aldo-Keto Reductases in the Eye |
title_full_unstemmed | Aldo-Keto Reductases in the Eye |
title_short | Aldo-Keto Reductases in the Eye |
title_sort | aldo-keto reductases in the eye |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902055/ https://www.ncbi.nlm.nih.gov/pubmed/20628518 http://dx.doi.org/10.1155/2010/521204 |
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