小干扰RNA
亚精胺
巨噬细胞极化
炎症
DNA损伤
药物输送
巨噬细胞
体内
细胞生物学
药理学
癌症研究
体外
化学
生物
免疫学
DNA
材料科学
转染
纳米技术
细胞培养
生物化学
酶
生物技术
遗传学
作者
Chaowang Huang,Qianyi You,Jing Xu,Di Wu,Huaping Chen,Yuhang Guo,Jiancheng Xu,Mingdong Hu,Hang Qian
标识
DOI:10.1002/adhm.202200008
摘要
Acute lung injury (ALI) is characterized by severe inflammation and damage to the lung air-blood barrier, resulting in respiratory function damage and life-threatening outcomes. Macrophage polarization plays an essential role in the occurrence, development, and outcome of ALI. As drug carriers, self-assembled DNA nanostructures can potentially overcome the drawbacks and limitations of traditional anti-inflammatory agents owing to their nontoxicity, programmability, and excellent structural control at the nanoscale. A small interfering RNA (siRNA) and drug dual therapy nanoplatform are proposed and constructed here to combat ALI. The nanoplatform consists of a spermidine-assembled DNA tetrahedron and four mammalian target of rapamycin siRNAs. Spermidine serves as a mediator of drug delivery vehicle synthesis and a drug that alters macrophage polarization. Both spermidine and siRNA exert anti-inflammatory effects in vitro and in vivo by regulating the macrophage phenotype. More importantly, these factors exhibit a synergistic anti-inflammatory effect by promoting macrophage autophagy. For the first time, an anti-inflammatory dual therapy strategy that uses self-assembled DNA nanostructures as nontoxic, programmable delivery vehicles is proposed and demonstrated through this work. Future work on utilizing DNA nanostructures for the treatment of noncancerous diseases such as ALI is highly promising and desirable.
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