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Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury

BACKGROUND: The purpose of this study was to determine whether elevated glucose can induce a dermal microvascular endothelial cell metabolic memory, thus affecting angiogenesis in the repair process of mammalian cutaneous wound. We hypothesized that transient elevated glucose levels cause sustained...

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Autores principales: Wang, Qiuyun, Song, Fei, Dong, Jiaoyun, Qiao, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246238/
https://www.ncbi.nlm.nih.gov/pubmed/34268371
http://dx.doi.org/10.21037/atm-20-7617
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author Wang, Qiuyun
Song, Fei
Dong, Jiaoyun
Qiao, Liang
author_facet Wang, Qiuyun
Song, Fei
Dong, Jiaoyun
Qiao, Liang
author_sort Wang, Qiuyun
collection PubMed
description BACKGROUND: The purpose of this study was to determine whether elevated glucose can induce a dermal microvascular endothelial cell metabolic memory, thus affecting angiogenesis in the repair process of mammalian cutaneous wound. We hypothesized that transient elevated glucose levels cause sustained alteration of endothelial cell responses to injury and persistent epigenetic changes in gene expression. METHODS: Human dermal microvascular endothelial cells were exposed to experimental conditions with or without 30 mM D-glucose. The control group was maintained at 5 mM D-glucose; while in the transient glucose group, after being exposed to 30 mM D-glucose for two days, then being put under the control conditions during the experiment. Besides, in the whole process of the experiment, the chronic glucose group was kept in the condition with 30 mM D-glucose. Proliferation, migration, tube formation, gene expression and histone methylation were assessed for individual conditions. RESULTS: Transient elevated glucose caused sustained effects on endothelial cell migration, tube formation and TIMP3 gene expression. The effects on TIMP3 expression were associated with persistent changes in histone modification at the 5' end of the TIMP3 gene, suggesting an epigenetic effect. CONCLUSIONS: Hyperglycemia induced metabolic memory could promote the regulation of TIMP3, and it can be used as a possible innovative molecular target for therapeutic intervention in the treatment of chronic non-healing diabetic wounds.
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spelling pubmed-82462382021-07-14 Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury Wang, Qiuyun Song, Fei Dong, Jiaoyun Qiao, Liang Ann Transl Med Original Article BACKGROUND: The purpose of this study was to determine whether elevated glucose can induce a dermal microvascular endothelial cell metabolic memory, thus affecting angiogenesis in the repair process of mammalian cutaneous wound. We hypothesized that transient elevated glucose levels cause sustained alteration of endothelial cell responses to injury and persistent epigenetic changes in gene expression. METHODS: Human dermal microvascular endothelial cells were exposed to experimental conditions with or without 30 mM D-glucose. The control group was maintained at 5 mM D-glucose; while in the transient glucose group, after being exposed to 30 mM D-glucose for two days, then being put under the control conditions during the experiment. Besides, in the whole process of the experiment, the chronic glucose group was kept in the condition with 30 mM D-glucose. Proliferation, migration, tube formation, gene expression and histone methylation were assessed for individual conditions. RESULTS: Transient elevated glucose caused sustained effects on endothelial cell migration, tube formation and TIMP3 gene expression. The effects on TIMP3 expression were associated with persistent changes in histone modification at the 5' end of the TIMP3 gene, suggesting an epigenetic effect. CONCLUSIONS: Hyperglycemia induced metabolic memory could promote the regulation of TIMP3, and it can be used as a possible innovative molecular target for therapeutic intervention in the treatment of chronic non-healing diabetic wounds. AME Publishing Company 2021-05 /pmc/articles/PMC8246238/ /pubmed/34268371 http://dx.doi.org/10.21037/atm-20-7617 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Wang, Qiuyun
Song, Fei
Dong, Jiaoyun
Qiao, Liang
Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title_full Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title_fullStr Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title_full_unstemmed Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title_short Transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
title_sort transient exposure to elevated glucose levels causes persistent changes in dermal microvascular endothelial cell responses to injury
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246238/
https://www.ncbi.nlm.nih.gov/pubmed/34268371
http://dx.doi.org/10.21037/atm-20-7617
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