心肌梗塞
纳米颗粒
长非编码RNA
小干扰RNA
心脏病学
核糖核酸
内科学
材料科学
医学
纳米技术
化学
基因
生物化学
作者
Meng Gao,Lianhong Yin,Bo Zhang,Zhichao Dong,Wenjiao Jiang,Zhuoya Bai,Xuerong Zhao,Lina Xu,Ning Wang,Jinyong Peng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-05-08
卷期号:19 (19): 18475-18491
被引量:5
标识
DOI:10.1021/acsnano.5c01641
摘要
mice), and lncRNA AK156373 knockout obviously reduced the infarct size, collagen fiber deposition, and ischemia severity in MI mice, leading to improved cardiac function. Additionally, lncRNA AK156373 modulated miR-204-5p to regulate C-X-C motif chemokine receptor 2 (CXCR2) protein expression via the competing endogenous RNA (ceRNA) mechanism, exacerbating myocardial damage and accelerating MI progression. Subsequently, nanoparticles loaded with lncRNA AK156373 siRNA were synthesized. The nanoparticles significantly inhibited MI progression by modulating the miR-204-5p/CXCR2 axis to reduce oxidative stress and inflammation. Overall, these findings establish a key regulatory role for lncRNA AK156373 in MI progression and present a direct preclinical approach for MI therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI