小RNA
张力素
PTEN公司
重性抑郁障碍
炎症
体内
萧条(经济学)
PI3K/AKT/mTOR通路
癌症研究
材料科学
医学
细胞生物学
内科学
生物
信号转导
基因
遗传学
经济
宏观经济学
扁桃形结构
作者
Yuling Luo,Xiao Yang,Yue Du,Yikai Dou,Weitong Cui,Jiajie Li,Jinxue Wei,Xiaohong Ma,Yunfeng Lin
标识
DOI:10.1021/acsami.3c03054
摘要
Major depressive disorder (MDD) is a common illness with an increasing lifetime prevalence. Thus, an increasing number of studies have investigated the association between MDD and microRNAs (miRNAs), which are a novel approach for treating depression. However, the therapeutic potential of miRNA-based strategies has several limitations. To overcome these limitations, DNA tetrahedra (TDNs) have been used as piggyback materials. In this study, we successfully used TDNs as carriers of miRNA-22-3p (miR-22-3p) and synthesized a novel DNA nanocomplex (TDN-miR-22-3p), which was used in a lipopolysaccharide (LPS)-induced depression cell model. The results suggest that miR-22-3p may regulate inflammation by regulating phosphatase and tensin homologue (PTEN), an important regulatory molecule in the PI3K/AKT pathway, and downregulating the expression of NLRP3. We further validated the role of TDN-miR-22-3p in vivo using an LPS-induced animal model of depression. The results indicate that it ameliorated depression-like behavior and attenuated the expression of inflammation-related factors in mice. This study demonstrates the establishment of a straightforward and efficacious miRNA delivery system and the potential of TDNs as therapeutic vectors and tools for mechanistic studies. To the best of our knowledge, this is the first study to use TDNs in combination with miRNAs to treat depression.
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