Small extracellular vesicles associated miRNA in myocardial fibrosis

被引：1
作者：
Long, Minwen [1 ]
Cheng, Min [1 ]
机构：
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Cardiol, Wuhan, Peoples R China
来源：
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 2024年 / 727卷
基金：
中国国家自然科学基金;
关键词：
Small extracellular vesicles; miRNA; Myocardial fibrosis; Stem cells; MESENCHYMAL STEM-CELLS; INHIBIT CARDIOMYOCYTE APOPTOSIS; CHRONIC KIDNEY-DISEASE; CARDIAC-FUNCTION; ATRIAL-FIBRILLATION; HEART-FAILURE; STROKE RISK; EXOSOMES; INFARCTION; MATRIX;
D O I：
10.1016/j.bbrc.2024.150336
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Myocardial fibrosis involves the loss of cardiomyocytes, myocardial fibroblast proliferation, and a reduction in angiogenesis, ultimately leading to heart failure, Given its significant implications, it is crucial to explore novel therapies for myocardial fibrosis. Recently one emerging avenue has been the use of small extracellular vesicles (sEV)-carried miRNA. In this review, we summarize the regulatory role of sEV-carried miRNA in myocardial fibrosis. We explored not only the potential diagnostic value of circulating miRNA as biomarkers for heart disease but also the therapeutic implications of sEV-carried miRNA derived from various cellular sources and applications of modified sEV. This exploration is paramount for researchers striving to develop innovative, cell-free therapies as potential drug candidates for the management of myocardial fibrosis.
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页数：15
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