促炎细胞因子
材料科学
体内
小胶质细胞
炎症
背景(考古学)
生物相容性
癌症研究
医学
药理学
免疫学
生物
生物技术
古生物学
冶金
作者
Wei Fu,Lu Ma,Yan Ju,Jianguo Xu,Hao Li,Sirong Shi,Tao Zhang,Ronghui Zhou,Jianwei Zhu,Ruxiang Xu,Chao You,Yunfeng Lin
标识
DOI:10.1002/adfm.202101435
摘要
Abstract Modulating microglial polarization is a potential strategy to assuage secondary brain injury caused by intracranial hemorrhage (ICH). However, despite decades of effort, effective therapies targeting microglia for ICH are still lacking. Here, a nanorobotic, tetrahedral framework nucleic acid (tFNA), is successfully synthesized and designed to carry C‐C chemokine receptor 2 (siCCR2) for use in in vitro hemin‐induced and in vivo collagenase‐induced ICH models. This nanoscale complex (tFNA‐siCCR2), which possesses biocompatibility, editability, and structural stability, exhibits a favorable effect in inhibiting the expression of CCR2 . After treatment with tFNA‐siCCR2, hematoma absorption is accelerated, and neurological inflammation is mitigated by decreasing levels of proinflammatory cytokines, while increasing the release of anti‐inflammatory factors. Consequently, the neurological deficits of mice with ICH improve. These results indicate that inhibiting CCR2 expression during the acute phase of ICH polarizes microglia towards a therapeutic subtype, and restores neurological function, which demonstrates that tFNA has a promising ability to transfer siCCR2 for treating ICH.
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