内皮干细胞
背景(考古学)
VCAM-1
内皮
基因传递
转染
癌症研究
化学
医学
细胞生物学
细胞粘附
细胞
生物
生物化学
体外
基因
内科学
古生物学
作者
Nicholas Distasio,Hugo Salmon,France Dierick,Talin Ebrahimian,Maryam Tabrizian,Stéphanie Lehoux
标识
DOI:10.1002/adtp.202000196
摘要
Abstract The ability to target nanoparticles to the dysfunctional endothelium may present a new and innovative therapy for cardiovascular disease. In this work, an anti‐inflammatory gene therapy nanoparticle targeted to VCAM‐1, a protein overexpressed by inflamed endothelial cells located within atherosclerotic plaque, is developed. Targeting is accomplished via a peptide‐grafted coating for the nanoparticles. Nanoparticle binding to VCAM‐1 is probed via surface plasmon resonance with imaging to determine kinetics and binding dynamics. Targeted nanoparticles are internalized by transfected inflamed primary endothelial cells more than nontargeted controls (80% vs 30% positive cells) under both static and dynamic flow conditions. The nanoparticles also bind specifically to VCAM‐1+ endothelial cells within atherosclerotic plaque from mouse models in both the aortic sinus and whole aorta. Taken together, this nanoparticle formulation may be an effective and specific strategy for anti‐inflammatory therapy within the context of atherosclerosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI