Magnetic Capture of Autologous Mesenchymal Stem Cells Promotes the Rapid Endothelialization of Peripheral Venous Stents in Rabbits.

Alexander A Oliver, Jonathan Cortese, Julien Ognard, Daying Dai, Esref A Bayraktar, Yong Hong Ding, Trace A Christensen, Scott I Gamb, Wasantha K Ranatunga, Kent D Carlson, Mukesh K Pandey, Roger J Guillory, Brandon J Tefft, Ramanathan Kadirvel, Dan Dragomir-Daescu, David F Kallmes
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Abstract

The rapid development of an endothelium over venous stents is associated with improved clinical outcomes. In this study, we investigate an approach to rapidly endothelialize venous stents using magnetic cell capture. Autologous mesenchymal stem cells were generated from rabbit adipose tissue and labeled with superparamagnetic iron oxide nanoparticles. Non-magnetic control and magnetic stents were deployed in the opposite external iliac veins of rabbits. The cells were delivered into the stent lumens in the presence of external magnets. Magnetic cell capture and retention, rate of endothelization, and stenosis were evaluated histologically. We found that the cells were capable of being magnetically captured by and adhering to the magnetic stents. Their magnetic capture facilitated the development of an endothelium over the magnetic stents within 3 days. In contrast, no magnetic cell capture was observed on the control stents, and the control stents were completely bare after 3 days. We found no significant difference in stenosis between the control and magnetic stents after 30 days. In conclusion, we demonstrated that autologous adipose derived mesenchymal stem cells labeled with superparamagnetic iron oxide nanoparticles are capable of being magnetically captured to the surface of magnetic stents, improving the rate of endothelialization in a rabbit iliac vein model. STATEMENT OF SIGNIFICANCE: Venous stents are deployed to mechanically open and restore blood flow through diseased, narrowed veins. Bare metal initially contacts blood, which may provoke thrombosis and neointimal hyperplasia leading to restenosis. Current drug‑eluting stents curb smooth muscle proliferation but delay endothelial healing, while antibody‑coated endothelial progenitor cell‑capturing stents accelerate healing but require permanent, expensive bioactive coatings. We studied autologous mesenchymal stem cells tagged with superparamagnetic iron‑oxide nanoparticles, magnetically drawn onto ferromagnetic stents by an external field. In a rabbit iliac vein model, this one‑time magnetic seeding significantly increased the rate of endothelialization on magnetic stents compared to non‑magnetic controls. This approach offers a mechanically simple, coating‑free route to improve venous stenting outcomes.

自体间充质干细胞磁捕获促进兔外周静脉支架快速内皮化。
血管内皮在静脉支架上的快速发展与临床结果的改善有关。在这项研究中,我们研究了一种利用磁细胞捕获快速内皮化静脉支架的方法。采用超顺磁性氧化铁纳米颗粒标记兔脂肪组织制备自体间充质干细胞。非磁性支架和磁性支架分别放置于家兔相对的髂外静脉。细胞在外部磁铁存在的情况下被送入支架管腔。组织学评价磁性细胞捕获和保留、内皮化率和狭窄程度。我们发现细胞能够被磁性支架捕获并粘附在磁性支架上。它们的磁性捕获有助于在3天内在磁性支架上形成内皮细胞。相比之下,在对照支架上没有观察到磁性细胞捕获,并且在3天后对照支架完全裸露。30天后,我们发现对照组和磁性支架之间的狭窄无显著差异。总之,我们证明了超顺磁性氧化铁纳米颗粒标记的自体脂肪来源的间充质干细胞能够被磁捕获到磁性支架表面,从而提高了兔髂静脉模型的内皮化率。意义说明:静脉支架的部署是为了机械地打开和恢复血液流过病变的、狭窄的静脉。裸金属最初接触血液,这可能引起血栓形成和新生内膜增生,导致再狭窄。目前的药物洗脱支架抑制平滑肌增殖,但延迟内皮细胞愈合,而抗体包被的内皮祖细胞捕获支架加速愈合,但需要永久的、昂贵的生物活性涂层。我们研究了用超顺磁性氧化铁纳米颗粒标记的自体间充质干细胞,通过外场将其磁性吸引到铁磁支架上。在兔髂静脉模型中,与非磁性对照组相比,这种一次性磁性植入显著增加了磁性支架上的内皮化率。这种方法提供了一种机械简单、无涂层的途径来改善静脉支架置入的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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