دورية أكاديمية
Cardiac-derived extracellular vesicles improve mitochondrial function to protect the heart against ischemia/reperfusion injury by delivering ATP5a1
العنوان: | Cardiac-derived extracellular vesicles improve mitochondrial function to protect the heart against ischemia/reperfusion injury by delivering ATP5a1 |
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المؤلفون: | Xuan Liu, Qingshu Meng, Shanshan Shi, Xuedi Geng, Enhao Wang, Yinzhen Li, Fang Lin, Xiaoting Liang, Xiaoling Xi, Wei Han, Huimin Fan, Xiaohui Zhou |
المصدر: | Journal of Nanobiotechnology, Vol 22, Iss 1, Pp 1-19 (2024) |
بيانات النشر: | BMC, 2024. |
سنة النشر: | 2024 |
المجموعة: | LCC:Biotechnology LCC:Medical technology |
مصطلحات موضوعية: | Extracellular vesicles, Myocardial ischemia-reperfusion, Mitochondria, Ferroptosis, ATP5a1, Biotechnology, TP248.13-248.65, Medical technology, R855-855.5 |
الوصف: | Abstract Background Numerous studies have confirmed the involvement of extracellular vesicles (EVs) in various physiological processes, including cellular death and tissue damage. Recently, we reported that EVs derived from ischemia-reperfusion heart exacerbate cardiac injury. However, the role of EVs from healthy heart tissue (heart-derived EVs, or cEVs) on myocardial ischemia-reperfusion (MI/R) injury remains unclear. Results Here, we demonstrated that intramyocardial administration of cEVs significantly enhanced cardiac function and reduced cardiac damage in murine MI/R injury models. cEVs treatment effectively inhibited ferroptosis and maintained mitochondrial homeostasis in cardiomyocytes subjected to ischemia-reperfusion injury. Further results revealed that cEVs can transfer ATP5a1 into cardiomyocytes, thereby suppressing mitochondrial ROS production, alleviating mitochondrial damage, and inhibiting cardiomyocyte ferroptosis. Knockdown of ATP5a1 abolished the protective effects of cEVs. Furthermore, we found that the majority of cEVs are derived from cardiomyocytes, and ATP5a1 in cEVs primarily originates from cardiomyocytes of the healthy murine heart. Moreover, we demonstrated that adipose-derived stem cells (ADSC)-derived EVs with ATP5a1 overexpression showed much better efficacy on the therapy of MI/R injury compared to control ADSC-derived EVs. Conclusions These findings emphasized the protective role of cEVs in cardiac injury and highlighted the therapeutic potential of targeting ATP5a1 as an important approach for managing myocardial damage induced by MI/R injury. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 1477-3155 |
Relation: | https://doaj.org/toc/1477-3155 |
DOI: | 10.1186/s12951-024-02618-x |
URL الوصول: | https://doaj.org/article/cccd6f4a630c4db795fd19e25af20bd2 |
رقم الأكسشن: | edsdoj.6f4a630c4db795fd19e25af20bd2 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 14773155 |
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DOI: | 10.1186/s12951-024-02618-x |