Department of Pharmacology and Center for Lung and Vascular Biology, College of Medicine, University of Illinois, Chicago, USA.
IUBMB Life. 2011 Aug;63(8):659-67. doi: 10.1002/iub.485. Epub 2011 Jul 15.
The endothelial cell monolayer lining the vessel wall forms a size-selective, semi-permeable barrier between the blood and tissue that must be crossed by blood borne therapeutic agents to reach diseased extravascular tissue. Nanoparticles engineered to carry drugs present an opportunity to enhance the specificity and efficacy of drug delivery. Therefore, an understanding of how these engineered nanoparticles are transported across the vessel wall will help us to more fully exploit this powerful therapeutic technology. Vascular endothelial cells are rich in caveolae, cell surface invaginations 50-100 nm in diameter that mediate endocytosis of lipids, proteins, and viruses. Caveolar invaginations pinch off to form intracellular vesicles that can transport cargo across the cell and release the cargo into the extravascular space via exocytosis. Here, we will review the current concepts and state of development for delivering engineered nanoparticles across the endothelium via the caveolae-mediated pathway.
血管壁内皮细胞单层形成了一个大小选择性的、半透性的屏障,血液中的治疗药物必须穿过这个屏障才能到达病变的血管外组织。设计用于携带药物的纳米颗粒为增强药物递送的特异性和疗效提供了机会。因此,了解这些工程纳米颗粒如何穿过血管壁将有助于我们更充分地利用这种强大的治疗技术。血管内皮细胞富含 caveolae,即直径为 50-100nm 的细胞表面内陷,介导脂质、蛋白质和病毒的内吞作用。caveolar 内陷会缢缩形成细胞内囊泡,可以将货物穿过细胞运输,并通过胞吐作用将货物释放到血管外空间。在这里,我们将回顾通过 caveolae 介导的途径将工程纳米颗粒递送到内皮细胞的当前概念和发展状况。