Cartaya Ana E, Lutz Halle, Maiocchi Sophie, Nalesnik Morgan, Bahnson Edward M
Department of Surgery, Division of Vascular Surgery, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Center for Nanotechnology in Drug Delivery, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Antioxidants (Basel). 2021 Apr 29;10(5):709. doi: 10.3390/antiox10050709.
Selective delivery of nuclear factor erythroid 2-related factor 2 (Nrf2) activators to the injured vasculature at the time of vascular surgical intervention has the potential to attenuate oxidative stress and decrease vascular smooth muscle cell (VSMC) hyperproliferation and migration towards the inner vessel wall. To this end, we developed a nanoformulation of cinnamic aldehyde (CA), termed Antioxidant Response Activating nanoParticles (ARAPas), that can be readily loaded into macrophages ex vivo. The CA-ARAPas-macrophage system was used to study the effects of CA on VSMC in culture. CA was encapsulated into a pluronic micelle that was readily loaded into both murine and human macrophages. CA-ARAPas inhibits VSMC proliferation and migration, and activates Nrf2. Macrophage-mediated transfer of CA-ARAPas to VSMC is evident after 12 h, and Nrf2 activation is apparent after 24 h. This is the first report, to the best of our knowledge, of CA encapsulation in pluronic micelles for macrophage-mediated delivery studies. The results of this study highlight the feasibility of CA encapsulation and subsequent macrophage uptake for delivery of cargo into other pertinent cells, such as VSMC.
在血管外科手术干预时,将核因子红细胞2相关因子2(Nrf2)激活剂选择性递送至受损血管系统,有可能减轻氧化应激,并减少血管平滑肌细胞(VSMC)的过度增殖以及向血管内壁的迁移。为此,我们开发了一种肉桂醛(CA)的纳米制剂,称为抗氧化反应激活纳米颗粒(ARAPas),它可以在体外轻松加载到巨噬细胞中。利用CA-ARAPas-巨噬细胞系统研究了CA对培养的VSMC的影响。CA被包裹在一种普朗尼克胶束中,这种胶束很容易加载到小鼠和人类巨噬细胞中。CA-ARAPas可抑制VSMC的增殖和迁移,并激活Nrf2。12小时后,巨噬细胞介导的CA-ARAPas向VSMC的转移很明显,24小时后Nrf2激活明显。据我们所知,这是关于将CA包裹在普朗尼克胶束中用于巨噬细胞介导的递送研究的首次报道。这项研究的结果突出了CA包裹以及随后巨噬细胞摄取以将货物递送至其他相关细胞(如VSMC)的可行性。