Department of Neurosurgery, Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, 310016, People's Republic of China.
Key Laboratory of Precise Treatment and Clinical Translational Research of Neurological Diseases, Hangzhou, 310016, People's Republic of China.
Int J Nanomedicine. 2024 Sep 2;19:8987-9007. doi: 10.2147/IJN.S473611. eCollection 2024.
Intracerebral hemorrhage (ICH) is a primary, non-traumatic cerebral event associated with substantial mortality and disability. Despite advancements in understanding its etiology and refining diagnostic techniques, a validated treatment to significantly improve ICH prognosis remains elusive. Exosomes, a subtype of extracellular vesicles, encapsulate bioactive components, predominantly microRNAs (miRNAs), facilitating and regulating intercellular communication. Currently, exosomes have garnered considerable interests in clinical transformation for their nanostructure, minimal immunogenicity, low toxicity, inherent stability, and the ability to traverse the blood-brain barrier. A wealth of studies has demonstrated that exosomes can improve the prognosis of ICH through anti-apoptosis, neurogenesis, angiogenesis, anti-inflammation, immunomodulation, and autophagy, primarily via the transportation or overexpression of selected miRNAs. More importantly, exosomes can be easily customized with specific miRNAs or bioactive compounds to establish delivery systems, broadening their potential applications. This review focuses on the therapeutic potential of exosomes in ICH, reviewing the mechanisms of molecular biology mediated by certain miRNAs, discussing the benefits, challenges, and future prospects in ICH treatment. We hope comprehensive understanding of exosomes based on miRNAs will provide new insights into the treatment of ICH and guide the translation of exosome's research from laboratory to clinical practice.
脑出血 (ICH) 是一种与高死亡率和高残疾率相关的原发性非外伤性脑事件。尽管在了解其病因和改进诊断技术方面取得了进展,但仍缺乏一种经证实可显著改善 ICH 预后的治疗方法。外泌体是细胞外囊泡的一种亚型,可包裹生物活性成分,主要是 microRNAs (miRNAs),从而促进和调节细胞间的通讯。目前,外泌体因其纳米结构、低免疫原性、低毒性、固有稳定性和穿越血脑屏障的能力,在临床转化方面引起了广泛关注。大量研究表明,外泌体可以通过抗细胞凋亡、神经发生、血管生成、抗炎、免疫调节和自噬来改善 ICH 的预后,主要通过运输或过表达选定的 miRNAs。更重要的是,外泌体可以很容易地用特定的 miRNAs 或生物活性化合物进行定制,以建立递药系统,从而拓宽它们的潜在应用。本综述重点关注外泌体在 ICH 中的治疗潜力,综述了特定 miRNAs 介导的分子生物学机制,并讨论了在 ICH 治疗中的益处、挑战和未来前景。我们希望基于 miRNAs 对细胞外泌体的全面了解,能为 ICH 的治疗提供新的见解,并指导外泌体研究从实验室向临床实践的转化。