The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction

Microvascular dysfunction (MVD) has long plagued the medical field despite improvements in its prevention, diagnosis, and intervention. Microvascular lesions from MVD increase with age and further lead to impaired microcirculation, target organ dysfunction, and a mass of microvascular complications,...

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Main Authors: Ye-Ran Zhang, Jiang-Dong Ji, Jia-Nan Wang, Ying Wang, Hong-Jing Zhu, Ru-Xu Sun, Qing-Huai Liu, Xue Chen
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Cells
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Online Access:https://www.mdpi.com/2073-4409/11/20/3193
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author Ye-Ran Zhang
Jiang-Dong Ji
Jia-Nan Wang
Ying Wang
Hong-Jing Zhu
Ru-Xu Sun
Qing-Huai Liu
Xue Chen
author_facet Ye-Ran Zhang
Jiang-Dong Ji
Jia-Nan Wang
Ying Wang
Hong-Jing Zhu
Ru-Xu Sun
Qing-Huai Liu
Xue Chen
author_sort Ye-Ran Zhang
collection DOAJ
description Microvascular dysfunction (MVD) has long plagued the medical field despite improvements in its prevention, diagnosis, and intervention. Microvascular lesions from MVD increase with age and further lead to impaired microcirculation, target organ dysfunction, and a mass of microvascular complications, thus contributing to a heavy medical burden and rising disability rates. An up-to-date understanding of molecular mechanisms underlying MVD will facilitate discoveries of more effective therapeutic strategies. Recent advances in epigenetics have revealed that RNA methylation, an epigenetic modification, has a pivotal role in vascular events. The N<sup>6</sup>-methylation of adenosine (m<sup>6</sup>A) modification is the most prevalent internal RNA modification in eukaryotic cells, which regulates vascular transcripts through splicing, degradation, translation, as well as translocation, thus maintaining microvascular homeostasis. Conversely, the disruption of the m<sup>6</sup>A regulatory network will lead to MVD. Herein, we provide a review discussing how m<sup>6</sup>A methylation interacts with MVD. We also focus on alterations of the m<sup>6</sup>A regulatory network under pathological conditions. Finally, we highlight the value of m<sup>6</sup>A regulators as prognostic biomarkers and novel therapeutic targets, which might be a promising addition to clinical medicine.
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spelling doaj.art-daa4e6f78fe7469c88ebd8fb4fe61a622023-11-23T23:27:06ZengMDPI AGCells2073-44092022-10-011120319310.3390/cells11203193The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular DysfunctionYe-Ran Zhang0Jiang-Dong Ji1Jia-Nan Wang2Ying Wang3Hong-Jing Zhu4Ru-Xu Sun5Qing-Huai Liu6Xue Chen7Department of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaDepartment of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University, Nanjing 210029, ChinaMicrovascular dysfunction (MVD) has long plagued the medical field despite improvements in its prevention, diagnosis, and intervention. Microvascular lesions from MVD increase with age and further lead to impaired microcirculation, target organ dysfunction, and a mass of microvascular complications, thus contributing to a heavy medical burden and rising disability rates. An up-to-date understanding of molecular mechanisms underlying MVD will facilitate discoveries of more effective therapeutic strategies. Recent advances in epigenetics have revealed that RNA methylation, an epigenetic modification, has a pivotal role in vascular events. The N<sup>6</sup>-methylation of adenosine (m<sup>6</sup>A) modification is the most prevalent internal RNA modification in eukaryotic cells, which regulates vascular transcripts through splicing, degradation, translation, as well as translocation, thus maintaining microvascular homeostasis. Conversely, the disruption of the m<sup>6</sup>A regulatory network will lead to MVD. Herein, we provide a review discussing how m<sup>6</sup>A methylation interacts with MVD. We also focus on alterations of the m<sup>6</sup>A regulatory network under pathological conditions. Finally, we highlight the value of m<sup>6</sup>A regulators as prognostic biomarkers and novel therapeutic targets, which might be a promising addition to clinical medicine.https://www.mdpi.com/2073-4409/11/20/3193N<sup>6</sup>-methyladenosine modificationangiogenesismicrovascular dysfunctionsepigenetics
spellingShingle Ye-Ran Zhang
Jiang-Dong Ji
Jia-Nan Wang
Ying Wang
Hong-Jing Zhu
Ru-Xu Sun
Qing-Huai Liu
Xue Chen
The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
Cells
N<sup>6</sup>-methyladenosine modification
angiogenesis
microvascular dysfunctions
epigenetics
title The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
title_full The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
title_fullStr The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
title_full_unstemmed The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
title_short The Role of N<sup>6</sup>-Methyladenosine Modification in Microvascular Dysfunction
title_sort role of n sup 6 sup methyladenosine modification in microvascular dysfunction
topic N<sup>6</sup>-methyladenosine modification
angiogenesis
microvascular dysfunctions
epigenetics
url https://www.mdpi.com/2073-4409/11/20/3193
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