ACS Nano. 2019 Feb 26;13(2):1272-1283. doi: 10.1021/acsnano.8b06572. Epub 2019 Jan 28.
Ischemic stroke is an acute and severe neurological disease, resulting in disability and death. Reperfusion to an ischemic brain is a means to reverse brain damage after stroke; however, this causes secondary tissue damage induced by inflammation responses, called ischemia/reperfusion (I/R) injury. Adhesion of neutrophils to endothelial cells underlies the initiation of inflammation in I/R. Inspired by this interaction, we report a drug delivery system comprised of neutrophil membrane-derived nanovesicles loaded with Resolvin D2 (RvD2) that can enhance resolution of inflammation, thus protecting brain damage during ischemic stroke. In the study, the middle cerebral artery occlusion (MCAO) mouse model was developed to mimic ischemic stroke. Using intravital microscopy of a live mouse brain, we visualized the binding of nanovesicles to inflamed brain vasculature for delivery of therapeutics to ischemic stroke lesions in real-time. We also observed that RvD2-loaded nanovesicles dramatically decreased inflammation in ischemic stroke and improved mouse neurological functions. Our study provides a strategy to inhibit neuroinflammation using neutrophil-derived nanovesicles for ischemic stroke therapy.
缺血性脑卒中是一种急性且严重的神经系统疾病,可导致残疾和死亡。对缺血性大脑进行再灌注是中风后逆转脑损伤的一种手段;然而,这会导致炎症反应引起的继发性组织损伤,称为缺血/再灌注 (I/R) 损伤。中性粒细胞与内皮细胞的黏附是 I/R 中炎症起始的基础。受此相互作用的启发,我们报告了一种由负载有 Resolvin D2 (RvD2) 的中性粒细胞膜衍生的纳米囊泡组成的药物递送系统,该系统可以增强炎症的消退,从而在缺血性脑卒中期间保护脑损伤。在该研究中,通过建立大脑中动脉闭塞 (MCAO) 小鼠模型来模拟缺血性脑卒中。通过对活体小鼠大脑的活体显微镜观察,我们实时观察到纳米囊泡与发炎的大脑血管结合,将治疗药物递送到缺血性脑卒中病变部位。我们还观察到负载 RvD2 的纳米囊泡可显著减轻缺血性脑卒中的炎症反应,并改善小鼠的神经功能。我们的研究为使用中性粒细胞衍生的纳米囊泡抑制神经炎症以治疗缺血性脑卒中提供了一种策略。