Vascular Repair by Circumferential Cell Therapy Using Magnetic Nanoparticles and Tailored Magnets

• Published in: ACS nano 2016-01, Vol.10 (1), p.369-376
• Main Authors: Vosen, Sarah, Rieck, Sarah, Heidsieck, Alexandra, Mykhaylyk, Olga, Zimmermann, Katrin, Bloch, Wilhelm, Eberbeck, Dietmar, Plank, Christian, Gleich, Bernhard, Pfeifer, Alexander, Fleischmann, Bernd K, Wenzel, Daniela
• Format: Article
• Language: English
• Subjects: Animals; Carotid Artery, Common - cytology; Carotid Artery, Common - metabolism; Carotid Artery, Common - surgery; Cell- and Tissue-Based Therapy - methods; Endothelial Cells - cytology; Endothelial Cells - enzymology; Endothelial Cells - transplantation; Endothelium, Vascular - cytology; Endothelium, Vascular - metabolism; Endothelium, Vascular - surgery; Gene Expression; Genetic Vectors - chemistry; Genetic Vectors - metabolism; Green Fluorescent Proteins - genetics; Green Fluorescent Proteins - metabolism; Lentivirus - genetics; Lentivirus - metabolism; Magnetite Nanoparticles - chemistry; Magnets; Mice; Mice, Knockout; Nitric Oxide Synthase Type III - genetics; Nitric Oxide Synthase Type III - metabolism; Polyethyleneimine - chemistry; Recombinant Fusion Proteins - genetics; Recombinant Fusion Proteins - metabolism; Tissue Engineering; Transduction, Genetic; Transgenes
• ISSN: 1936-0851; 1936-086X
• DOI: 10.1021/acsnano.5b04996

Cardiovascular disease is often caused by endothelial cell (EC) dysfunction and atherosclerotic plaque formation at predilection sites. Also surgical procedures of plaque removal cause irreversible damage to the EC layer, inducing impairment of vascular function and restenosis. In the current study we have examined a potentially curative approach by radially symmetric re-endothelialization of vessels after their mechanical denudation. For this purpose a combination of nanotechnology with gene and cell therapy was applied to site-specifically re-endothelialize and restore vascular function. We have used complexes of lentiviral vectors and magnetic nanoparticles (MNPs) to overexpress the vasoprotective gene endothelial nitric oxide synthase (eNOS) in ECs. The MNP-loaded and eNOS-overexpressing cells were magnetic, and by magnetic fields they could be positioned at the vascular wall in a radially symmetric fashion even under flow conditions. We demonstrate that the treated vessels displayed enhanced eNOS expression and activity. Moreover, isometric force measurements revealed that EC replacement with eNOS-overexpressing cells restored endothelial function after vascular injury in eNOS–/– mice ex and in vivo. Thus, the combination of MNP-based gene and cell therapy with custom-made magnetic fields enables circumferential re-endothelialization of vessels and improvement of vascular function.