下调和上调
小干扰RNA
TLR2型
核酸
先天免疫系统
基因沉默
败血症
Toll样受体
TLR4型
RNA干扰
受体
脂多糖
CD14型
核糖核酸
模式识别受体
细胞生物学
生物
基因
免疫学
信号转导
生物化学
作者
Xiaolin Zhang,Mei Zhang,Mi Zhou,Tao Zhang,Yang Gao,Songhang Li,Yunfeng Lin,Xiaoxiao Cai
标识
DOI:10.1021/acsami.1c23708
摘要
Sepsis is caused by the invasion of pathogenic microorganisms, which can lead to excessive expression of toll-like receptors (TLRs) in cells and uncontrollable amplification of the inflammatory response. TLR2, as an essential part of the TLR family, has a significant feature in the identification of innate immune responses. Therefore, blocking the expression and activation of TLR2 can inhibit the synthesis and release of inflammatory factors and avoid the occurrence of excessive inflammatory reactions. Small interfering RNA (siRNA) can selectively target the silencing or downregulation of pathogenic genes and has the advantages of high specificity, a strong effect, and fewer adverse reactions. However, the application of siRNA is limited by its high molecular weight, poor biostability, and difficulty in passive uptake into cells. Tetrahedral-framework nucleic acid (tFNA) is a new kind of three-dimensional nucleic acid nanomaterial, which has the advantages of good biocompatibility, stable structure, and editability. In this study, we used tFNA as carriers to deliver siRNA-targeting downregulation of TLR2 expression for anti-inflammatory therapy. We show that siRNA can specifically reduce lipopolysaccharide (LPS)-induced TLR2 elevation and reduce release of inflammatory factors in LPS-induced experimental sepsis, which provides a new idea for the prevention and treatment of sepsis.
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