Hassanzadeh Ali, Shomali Navid, Kamrani Amin, Nasiri Hadi, Ahmadian Heris Javad, Pashaiasl Maryam, Sadeghi Mohammadreza, Sadeghvand Shahram, Valedkarimi Zahra, Akbari Morteza
Department of Applied Cell Sciences, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Department of Immunology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
EXCLI J. 2024 Mar 25;23:401-420. doi: 10.17179/excli2023-6538. eCollection 2024.
Coronary heart disease (CHD) continues to be the leading cause of morbidity and mortality. There are numerous therapeutic reperfusion methods, including thrombolytic therapy, primary percutaneous coronary intervention, and anti-remodeling drugs like angiotensin-converting enzyme inhibitors and beta-blockers. Despite this, there is no pharmacological treatment that can effectively stop cardiomyocyte death brought on by myocardial ischemia/reperfusion (I/R) injury. For the purpose of regenerating cardiac tissue, mesenchymal stem cell (MSC) therapy has recently gained more attention. The pleiotropic effects of MSCs are instead arbitrated by the secretion of soluble paracrine factors and are unrelated to their capacity for differentiation. One of these paracrine mediators is the extracellular vesicle known as an exosome. Exosomes deliver useful cargo to recipient cells from MSCs, including peptides, proteins, cytokines, lipids, miRNA, and mRNA molecules. Exosomes take part in intercellular communication processes and help tissues and organs that have been injured or are ill heal. Exosomes alone were found to be the cause of MSCs' therapeutic effects in a variety of animal models, according to studies. Here, we have focused on the recent development in the therapeutic capabilities of exosomal MSCs in cardiac diseases.
冠心病(CHD)仍然是发病和死亡的主要原因。有多种治疗性再灌注方法,包括溶栓治疗、直接经皮冠状动脉介入治疗以及诸如血管紧张素转换酶抑制剂和β受体阻滞剂等抗重塑药物。尽管如此,尚无药物治疗能够有效阻止心肌缺血/再灌注(I/R)损伤导致的心肌细胞死亡。为了再生心脏组织,间充质干细胞(MSC)疗法最近受到了更多关注。相反,MSC的多效性作用是由可溶性旁分泌因子的分泌介导的,与其分化能力无关。这些旁分泌介质之一是被称为外泌体的细胞外囊泡。外泌体将有用的物质传递给来自MSC的受体细胞,包括肽、蛋白质、细胞因子、脂质、miRNA和mRNA分子。外泌体参与细胞间通讯过程,并帮助受伤或患病的组织和器官愈合。根据研究,在多种动物模型中发现外泌体本身就是MSC治疗作用的原因。在此,我们重点关注了外泌体MSC在心脏病治疗能力方面的最新进展。