归巢(生物学)
核酸
材料科学
小RNA
冲程(发动机)
肽
缺血性中风
肽核酸
医学
内科学
缺血
生物
生物化学
基因
机械工程
生态学
工程类
作者
Guannan Du,Yangxue Yao,Wen Chen,Yunfeng Lin,Yao He,Mi Zhou,Xiaoxiao Cai
标识
DOI:10.1021/acsami.5c00507
摘要
Acute ischemic stroke (AIS) is associated with a high mortality rate and poor prognosis, with a lack of effective therapeutic drugs for post-thrombolytic treatment. MicroRNA-based gene therapy is a promising approach for treating AIS, but its clinical application has been limited due to challenges, such as poor targeting efficiency, unsatisfactory stability, and inadequate cellular uptake. In this study, we successfully developed a microRNA-targeted delivery system based on the tetrahedral framework nucleic acid (tFNA). This nanodelivery system, guided by stroke-homing peptides, effectively targeted and delivered miRNA124 to the ischemic hemisphere. With the assistance of tFNA, miRNA124 efficiently entered cells and exerted therapeutic effects. Additionally, it promoted the transformation of microglia from the pro-inflammatory M1 phenotype to the anti-inflammatory M2 phenotype, reducing neuronal apoptosis and, ultimately, decreasing the infarct size and mortality rate. These findings present a promising therapeutic strategy for the targeted treatment of AIS.
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