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富集miR-29b的外泌体在心肌梗死后抑制心室重构的影响

郑伟 王晓明 韩志伟 邹龙 范晨亮 孙宏达 员建平

中国体外循环杂志2025,Vol.23Issue(3):258-262,268,6.
中国体外循环杂志2025,Vol.23Issue(3):258-262,268,6.DOI:10.13498/j.cnki.chin.j.ecc.2025.03.13

富集miR-29b的外泌体在心肌梗死后抑制心室重构的影响

Research on the role and mechanism of miR-29b-enriched exosomes in inhibiting post-myocardial infarction ventricular remodeling

郑伟 1王晓明 2韩志伟 2邹龙 2范晨亮 3孙宏达 3员建平2

作者信息

  • 1. 014000 包头,包头市中心医院心内科
  • 2. 014000 包头,包头市中心医院心血管外科
  • 3. 150050 哈尔滨,哈尔滨精神专科白鱼泡医院第 11 病区
  • 折叠

摘要

Abstract

Objective To investigate the role and underlying mechanisms of exosomes(EXOs)enriched with miR-29b in inhibiting post-myocardial infarction(MI)ventricular remodeling.Methods miR-29b-enriched EXOs were engineered via in vitro transfection and administered to MI-induced mice through tail vein injection.The experiment was divided into four groups:normal control,MI model,EXO-treated,and miR-29b-enriched EXO-treated.Cardiac function,ventricular remodeling,and related molecular mechanisms were assessed using echocardiography,histopathological staining,and Western blot analysis.Results Compared to the MI model group,miR-29b-enriched EXO treatment significant improved post-MI cardiac function,in the miR-29b-enriched EXO group.miR-29b overexpression in cardiac tissue correlated with downregulated collagen I and collagen III expression.Conclusion Tail vein injection of miR-29b-enriched EXOs effectively suppresses ventricular remodeling post-MI by targeting myocardial fibrosis.This study highlights the potential of miRNA-engineered exosomes as a novel therapeutic strategy for cardiovascular diseases.

关键词

急性心肌梗死/外泌体/miR-29b/心室重构/心肌纤维化

Key words

Acute myocardial infarction/Exosome/miR-29b/Ventricular remodeling/Myocardial fibrosis

引用本文复制引用

郑伟,王晓明,韩志伟,邹龙,范晨亮,孙宏达,员建平..富集miR-29b的外泌体在心肌梗死后抑制心室重构的影响[J].中国体外循环杂志,2025,23(3):258-262,268,6.

基金项目

内蒙古自治区自然科学基金资助项目(2022LHMS08014) (2022LHMS08014)

内蒙古医科大学联合项目(YKD2021LH093) (YKD2021LH093)

内蒙古自治区2022年卫生健康科技计划项目(202201508) (202201508)

中国体外循环杂志

1672-1403

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