基因敲除
小干扰RNA
基因沉默
体内
RNA干扰
炎症
体外
基因表达
细胞生物学
脂多糖
化学
癌症研究
药理学
核糖核酸
医学
生物
基因
免疫学
生物化学
生物技术
作者
Taewon Jeon,David C. Luther,Ritabrita Goswami,C E Bell,Harini Nagaraj,Yağız Anıl Çiçek,Rui Huang,Javier A. Mas‐Rosario,James L. Elia,Jungkyun Im,Yi-Wei Lee,Yuanchang Liu,Federica Scaletti,Michelle E. Farkas,Jesse Mager,Vincent M. Rotello
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-02-20
卷期号:17 (5): 4315-4326
被引量:13
标识
DOI:10.1021/acsnano.2c08690
摘要
Uncontrolled inflammation is responsible for acute and chronic diseases in the lung. Regulating expression of pro-inflammatory genes in pulmonary tissue using small interfering RNA (siRNA) is a promising approach to combatting respiratory diseases. However, siRNA therapeutics are generally hindered at the cellular level by endosomal entrapment of delivered cargo and at the organismal level by inefficient localization in pulmonary tissue. Here we report efficient anti-inflammatory activity in vitro and in vivo using polyplexes of siRNA and an engineered cationic polymer (PONI-Guan). PONI-Guan/siRNA polyplexes efficiently deliver siRNA cargo to the cytosol for highly efficient gene knockdown. Significantly, these polyplexes exhibit inherent targeting to inflamed lung tissue following intravenous administration in vivo. This strategy achieved effective (>70%) knockdown of gene expression in vitro and efficient (>80%) silencing of TNF-α expression in lipopolysaccharide (LPS)-challenged mice using a low (0.28 mg/kg) siRNA dosage.
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