Tetrahedral-Framework Nucleic Acids Carry Small Interfering RNA to Downregulate Toll-Like Receptor 2 Gene Expression for the Treatment of Sepsis.
Xiaolin ZhangMei ZhangMi ZhouTao ZhangYang GaoSonghang LiYunfeng LinXiaoxiao CaiPublished in: ACS applied materials & interfaces (2022)
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.
Keyphrases
- inflammatory response
- toll like receptor
- nucleic acid
- lps induced
- lipopolysaccharide induced
- immune response
- nuclear factor
- cancer therapy
- poor prognosis
- acute kidney injury
- gene expression
- intensive care unit
- induced apoptosis
- septic shock
- anti inflammatory
- oxidative stress
- signaling pathway
- cell proliferation
- cell cycle arrest
- binding protein
- weight gain
- drug delivery
- dna methylation
- risk assessment
- long non coding rna
- tissue engineering
- combination therapy
- emergency department
- bioinformatics analysis
- weight loss
- bone marrow
- stem cells