微泡
血管生成
旁分泌信号
小RNA
细胞生物学
生物
癌症研究
血管内皮生长因子
电池类型
细胞
医学
生物信息学
免疫学
基因
生物化学
血管内皮生长因子受体
受体
作者
Kasra Moeinabadi‐Bidgoli,Malihe Rezaee,Nikoo Hossein‐Khannazer,Amirhesam Babajani,Hamid Asadzadeh Aghdaei,Mandana Kazem Arki,Siamak Afaghi,Hassan Niknejad,Massoud Vosough
摘要
Abstract Ischaemic disorders are leading causes of morbidity and mortality worldwide. While the current therapeutic approaches have improved life expectancy and quality of life, they are unable to “cure” ischemic diseases and instate regeneration of damaged tissues. Exosomes are a class of extracellular vesicles with an average size of 100–150 nm, secreted by many cell types and considered a potent factor of cells for paracrine effects. Since exosomes contain multiple bioactive components such as growth factors, molecular intermediates of different intracellular pathways, microRNAs and nucleic acids, they are considered as cell‐free therapeutics. Besides, exosomes do not rise cell therapy concerns such as teratoma formation, alloreactivity and thrombotic events. In addition, exosomes are stored and utilized more convenient. Interestingly, exosomes could be an ideal complementary therapeutic tool for ischemic disorders. In this review, we discussed therapeutic functions of exosomes in ischemic disorders including angiogenesis induction through various mechanisms with specific attention to vascular endothelial growth factor pathway. Furthermore, different delivery routes of exosomes and different modification strategies including cell preconditioning, gene modification and bioconjugation, were highlighted. Finally, pre‐clinical and clinical investigations in which exosomes were used were discussed.
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