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拉蓬特®纳米硅酸盐增强了 FG-4592 的血管生成作用和 BMP-2 的成骨作用。

LAPONITE® nano-silicates potentiate the angiogenic effects of FG-4592 and osteogenic effects of BMP-2.

机构信息

Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA.

Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, 55905, USA.

出版信息

Biomater Sci. 2024 Oct 22;12(21):5610-5619. doi: 10.1039/d4bm00636d.

Abstract

LAPONITE®-based drug delivery systems offer many advantages due to the unique ionic and physical properties of LAPONITE®. The high ionicity and large surface area of LAPONITE® nanoparticles enable the intercalation and dissolution of biomolecules. In this study, we explored the potential of LAPONITE® as a carrier for FG-4592 to support angiogenesis and as a carrier for bone morphogenic protein-2 (BMP-2) to support osteogenesis. Interestingly, we found that LAPONITE® promoted the FG-4592 induced upregulation of vascular endothelial growth factor (VEGF) gene expression of human umbilical cord endothelial cells (HUVECs). Additionally, we observed that LAPONITE® could provide a sustained release of BMP-2 and significantly potentiate the osteogenic effects of BMP-2 on adipose derived mesenchymal stem cells (AMSCs). Overall, current findings on the LAPONITE®-drug/protein model system provide a unique way to potentiate the angiogenic activities of FG-4592 on HUVECs and osteogenic effects of BMP-2 on AMSCs for tissue engineering application. Future studies will be directed towards gaining a deeper understanding of these effects on a co-culture system of HUVECs and AMSCs.

摘要

基于 LAPONITE®的药物传递系统由于 LAPONITE®独特的离子和物理特性而具有许多优势。LAPONITE®纳米颗粒的高离子性和大表面积使生物分子能够插入和溶解。在这项研究中,我们探讨了 LAPONITE®作为 FG-4592 的载体支持血管生成和作为骨形态发生蛋白-2(BMP-2)的载体支持成骨的潜力。有趣的是,我们发现 LAPONITE®促进了 FG-4592 诱导的人脐静脉内皮细胞(HUVEC)血管内皮生长因子(VEGF)基因表达的上调。此外,我们观察到 LAPONITE®可以提供 BMP-2 的持续释放,并显著增强 BMP-2 对脂肪来源间充质干细胞(AMSCs)的成骨作用。总的来说,目前关于 LAPONITE®-药物/蛋白质模型系统的研究结果提供了一种独特的方法,可以增强 FG-4592 在 HUVEC 上的血管生成活性和 BMP-2 在 AMSCs 上的成骨作用,用于组织工程应用。未来的研究将致力于更深入地了解这些在 HUVEC 和 AMSCs 共培养系统中的作用。

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