Back to Search Start Over

High glucose promotes atherosclerosis by regulating miRNA let7d‐5p level

Authors :
Hua Wang
Fentao Liu
Wenyu Zhao
Yiting Guo
Peipei Mai
Songfeng Zhao
Zhiguo Wen
Jie Su
Xuan Li
Yunlong Wang
Yanfang Zhang
Source :
Journal of Diabetes Investigation, Vol 15, Iss 6, Pp 711-724 (2024)
Publication Year :
2024
Publisher :
Wiley, 2024.

Abstract

ABSTRACT Background MiRNA let7d‐5p has been recently reported to be abnormally expressed in diabetes‐associated atherosclerosis (AS). However, it still remains unknown how let7d‐5p contributes to the process of atherosclerosis. Methods Twenty fresh tissues and a total of 28 wax block specimens from carotid endarterectomy procedures were obtained from the Luoyang Central Hospital affiliated to Zhengzhou University. The expression of let7d‐5p was assessed using quantitative RT‐PCR (qRT‐PCR). A series of in vitro experiments was used to determine the roles of let7d‐5p knockdown and overexpression in vascular smooth muscle cells (VSMCs). Results We discovered that the carotid plaques from diabetic patients had lower expression levels of miR let7d‐5p. In VSMCs, the expression of miRNA let7d‐5p was significantly lower in high glucose conditions compared with low glucose situations. The proliferation and migration of VSMCs were also inhibited by the overexpression of let7d‐5p, whereas the opposite was true when let7d‐5p was inhibited, according to gain and loss of function studies. Mechanically, let7d‐5p might activate the GSK3β/β‐catenin signaling pathway via binding to the high mobility group AT‐Hook 2 (HMGA2) mRNA in VSMCs. Additionally, GLP‐1RA liraglutide may prevent the migration and proliferation of VSMCs by raising let7d‐5p levels. Conclusions High glucose stimulated the proliferation and migration of VSMCs by regulating the let7d‐5p/HMGA2/GSK3β/β‐catenin pathway, and liraglutide may slow atherosclerosis by increasing the levels of miR let7d‐5p.

Details

Language :
English
ISSN :
20401124 and 20401116
Volume :
15
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Journal of Diabetes Investigation
Publication Type :
Academic Journal
Accession number :
edsdoj.f4951f040e7d43aa836b4c753ec97fa8
Document Type :
article
Full Text :
https://doi.org/10.1111/jdi.14180