Department of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, Massachusetts 01609, USA.
J Biomed Mater Res A. 2011 Feb;96(2):301-12. doi: 10.1002/jbm.a.32978.
We developed a method to produce discrete fibrin microthreads, which can be seeded with human mesenchymal stem cells (hMSCs) and used as a suture to enhance the efficiency and localization of cell delivery. To assess the efficacy of fibrin microthreads to support hMSC attachment, proliferation, and survival, microthreads (100 μm diameter per microthread) were bundled together, seeded with 50,000 hMSCs for 2 h, and cultured for 5 days. Cell density on microthread bundles increased over time in culture to a maximum average density of 731 ± 101 cells/mm(2) after 5 days. A LIVE/DEAD assay confirmed that the cells were viable, and Ki-67 staining verified hMSC proliferation. In addition, functional differentiation assays demonstrated that hMSCs cultured on microthreads retained their ability to differentiate into adipocytes and osteocytes. The results of this study demonstrate that fibrin microthreads support hMSC viability and proliferation, while maintaining their multipotency. We anticipate that these cell-seeded fibrin microthreads will serve as a platform technology to improve localized delivery and engraftment of viable cells to damaged tissue.
我们开发了一种生产离散纤维蛋白微丝的方法,可以将其接种人骨髓间充质干细胞(hMSCs)并用作缝线,以提高细胞递送的效率和定位。为了评估纤维蛋白微丝对支持 hMSC 附着、增殖和存活的功效,将微丝(每条微丝直径 100μm)捆扎在一起,接种 50000 个 hMSC 培养 2 小时,然后培养 5 天。在培养过程中,随着时间的推移,微丝束上的细胞密度增加,5 天后平均密度最高达到 731±101 个细胞/mm2。LIVE/DEAD 检测证实细胞是存活的,Ki-67 染色证实 hMSC 增殖。此外,功能分化试验表明,在微丝上培养的 hMSCs 保留了分化为脂肪细胞和成骨细胞的能力。这项研究的结果表明,纤维蛋白微丝支持 hMSC 的存活和增殖,同时保持其多能性。我们预计,这些细胞接种的纤维蛋白微丝将作为一种平台技术,改善对受损组织的有活力细胞的局部递送和植入。