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Responses of retinal and brain microvasculature to streptozotocin induced diabetes revealed by global expression profiling
This study aims to determine the effects of diabetes in the retinal and brain microvasculature through gene expression profiling. Twelve male Wistar rats were randomly divided into two groups: streptozotocin-induced diabetic rats and time-matched nondiabetic rats. The retinal microvessels (RMVs) and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982389/ https://www.ncbi.nlm.nih.gov/pubmed/36606460 http://dx.doi.org/10.1177/14791641221147533 |
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author | Li, Youhai Faiz, Alen Moshage, Han Schilling, Lothar Kamps, Jan AAM |
author_facet | Li, Youhai Faiz, Alen Moshage, Han Schilling, Lothar Kamps, Jan AAM |
author_sort | Li, Youhai |
collection | PubMed |
description | This study aims to determine the effects of diabetes in the retinal and brain microvasculature through gene expression profiling. Twelve male Wistar rats were randomly divided into two groups: streptozotocin-induced diabetic rats and time-matched nondiabetic rats. The retinal microvessels (RMVs) and brain microvessels (BMVs) were mechanically isolated from individual rats. Differentially expressed genes (DEGs) in diabetic and nondiabetic microvessels were identified by cDNA microarrays analysis. In RMVs, we identified 43 DEGs, of which 20 were upregulated while 23 were downregulated by diabetes. In BMVs, 35 genes DEGs were identified, of which 22 were upregulated and 13 were downregulated by diabetes. Altered expression of the Nars, Gars, Mars, Iars, Yars, Bcl2, Nqo1, NR4A3, Gpd1, Stc1, Tsc22d3, Tnfrsf21 mRNA as observed in the microarray analyses, was confirmed by quantitative RT-PCR. The aminoacyl-tRNA synthetases (aaRSs) pathway in RMVs was significantly overrepresented as compared to BMVs. Our study demonstrates for the first time that in the brain microvasculature multiple compensatory mechanisms exists, serving to protect brain tissue from diabetic insults, whereas these mechanisms are not activated in the retinal microvasculature. This provides new insights as to why brain microvasculature is less susceptible to diabetes. |
format | Online Article Text |
id | pubmed-9982389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-99823892023-03-04 Responses of retinal and brain microvasculature to streptozotocin induced diabetes revealed by global expression profiling Li, Youhai Faiz, Alen Moshage, Han Schilling, Lothar Kamps, Jan AAM Diab Vasc Dis Res Original Article This study aims to determine the effects of diabetes in the retinal and brain microvasculature through gene expression profiling. Twelve male Wistar rats were randomly divided into two groups: streptozotocin-induced diabetic rats and time-matched nondiabetic rats. The retinal microvessels (RMVs) and brain microvessels (BMVs) were mechanically isolated from individual rats. Differentially expressed genes (DEGs) in diabetic and nondiabetic microvessels were identified by cDNA microarrays analysis. In RMVs, we identified 43 DEGs, of which 20 were upregulated while 23 were downregulated by diabetes. In BMVs, 35 genes DEGs were identified, of which 22 were upregulated and 13 were downregulated by diabetes. Altered expression of the Nars, Gars, Mars, Iars, Yars, Bcl2, Nqo1, NR4A3, Gpd1, Stc1, Tsc22d3, Tnfrsf21 mRNA as observed in the microarray analyses, was confirmed by quantitative RT-PCR. The aminoacyl-tRNA synthetases (aaRSs) pathway in RMVs was significantly overrepresented as compared to BMVs. Our study demonstrates for the first time that in the brain microvasculature multiple compensatory mechanisms exists, serving to protect brain tissue from diabetic insults, whereas these mechanisms are not activated in the retinal microvasculature. This provides new insights as to why brain microvasculature is less susceptible to diabetes. SAGE Publications 2023-01-06 /pmc/articles/PMC9982389/ /pubmed/36606460 http://dx.doi.org/10.1177/14791641221147533 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Li, Youhai Faiz, Alen Moshage, Han Schilling, Lothar Kamps, Jan AAM Responses of retinal and brain microvasculature to streptozotocin induced diabetes revealed by global expression profiling |
title | Responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
title_full | Responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
title_fullStr | Responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
title_full_unstemmed | Responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
title_short | Responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
title_sort | responses of retinal and brain microvasculature to streptozotocin
induced diabetes revealed by global expression profiling |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9982389/ https://www.ncbi.nlm.nih.gov/pubmed/36606460 http://dx.doi.org/10.1177/14791641221147533 |
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