自噬
材料科学
DNA甲基化
脂质体
阳离子脂质体
体内
细胞生物学
药理学
癌症研究
纳米技术
医学
转染
生物
生物化学
细胞凋亡
生物技术
基因表达
基因
作者
Yulin Li,Anning Yang,Yue Sun,Dayue Liu,Peidong You,Yaling Zeng,Shangkun Quan,Hongwen Zhang,Huiping Zhang,Shengchao Ma,Yinju Hao,Jiantuan Xiong,Bin Liu,Guizhong Li,Yideng Jiang
标识
DOI:10.1016/j.matdes.2023.111807
摘要
Cardiovascular disease (CVD) caused by atherosclerosis has become a main threaten for human health. As an independent risk factor, hyperhomocysteinemia (HHcy) played an important role in the pathogenesis of atherosclerosis by regulating DNA methylation modification and autophagy of macrophages. In this study, we constructed a new kind of macro-liposome nanoparticle by hybridizing liposome with macrophages membranes (Møm) to encapsulate hydroxysafflower yellow A (HSYA). Assertion of Hyaluronic acid (HA) on the macro-liposome NPs was adopted to endow nanodrug targeting ability. In vitro results showed that the prepared macro-liposome nanoparticles can significantly inhibit Atg13 DNA methylation, while enhance autophagy of macrophages to promote cholesterol efflux, as well. In vivo studies have shown that the HA modification made the macro-liposome NPs an ideal decoy for targeting plaques. Thus, the macro-liposome NPs with prolonged blood circulation time, and improved targeting ability can achieve optimal HSYA accumulation at the region of atherosclerotic plaques to obtain high efficacy. According to our point, the nano-drug delivery system with high immune escape capability provided a feasible therapeutic strategy for efficient atherosclerosis therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI