微泡
医学
疾病
外体
血管生成
分离(微生物学)
生物信息学
重症监护医学
小RNA
病理
癌症研究
生物
生物化学
基因
作者
Gui-hao Chen,Jun Xu,Yuejin Yang
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physical Society]
日期:2017-06-24
卷期号:313 (3): H508-H523
被引量:31
标识
DOI:10.1152/ajpheart.00213.2017
摘要
Ischemic heart disease(IHD) is the leading cause of death worldwide. Despite the development of continuously improving therapeutic strategies, morbidity and mortality of patients with IHD remain relatively high. Exosomes are a subpopulation of vesicles that are universally recognized as major mediators in intercellular communication. Numerous preclinical studies have shown that these tiny vesicles were protective in IHD, through such actions as alleviating myocardial ischemia-reperfusion injury, promoting angiogenesis, inhibiting fibrosis, and facilitating cardiac regeneration. Our review focused on these beneficial exosome-mediated processes. In addition, we discuss in detail how to fully exploit the therapeutic potentials of exosomes in the field of IHD. Topics include identifying robust sources of exosomes, loading protective agents into exosomes, developing heart-specific exosomes, optimizing isolation methods, and translating the cardioprotective effects of exosomes into clinical practice. Finally, both the advantages and disadvantages of utilizing exosomes in clinical settings are addressed.
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