Tenchurin Timur Kh, Rodina Alla V, Saprykin Vladimir P, Gorshkova Lada V, Mikhutkin Alexey A, Kamyshinsky Roman A, Yakovlev Dmitry S, Vasiliev Alexander L, Chvalun Sergey N, Grigoriev Timofey E
National Research Centre "Kurchatov Institute", 123098 Moscow, Russia.
Natural Sciences Department, Moscow Region State University, 105005 Moscow, Russia.
Polymers (Basel). 2022 Oct 15;14(20):4352. doi: 10.3390/polym14204352.
The 3D reconstruction of 100 μm- and 600 μm-thick fibrous poly-L/L-lactide scaffolds was performed by confocal laser scanning microscopy and supported by scanning electron microscopy and showed that the density of the fibers on the side adjacent to the electrode is higher, which can affect cell diffusion, while the pore size is generally the same. Bone marrow mesenchymal stem cells cultured in a 600 μm-thick scaffold formed colonies and produced conditions for cell differentiation. An in vitro study of stem cells after 7 days revealed that cell proliferation and hepatocyte growth factor release in the 600 μm-thick scaffold were higher than in the 100 μm-thick scaffold. An in vivo study of scaffolds with and without stem cells implanted subcutaneously onto the backs of recipient mice was carried out to test their biodegradation and biocompatibility over a 0-3-week period. The cells seeded onto the 600 μm-thick scaffold promoted significant neovascularization in vivo. After 3 weeks, a significant number of donor cells persisted only on the inside of the 600 μm-thick scaffold. Thus, the use of bulkier matrices allows to prolong the effect of secretion of growth factors by stem cells during implantation. These 600 μm-thick scaffolds could potentially be utilized to repair and regenerate injuries with stem cell co-culture for vascularization of implant.
通过共聚焦激光扫描显微镜对100μm厚和600μm厚的纤维状聚L/L-丙交酯支架进行三维重建,并辅以扫描电子显微镜,结果显示靠近电极一侧的纤维密度更高,这可能会影响细胞扩散,而孔径通常相同。在600μm厚的支架中培养的骨髓间充质干细胞形成了集落,并为细胞分化创造了条件。对干细胞进行7天的体外研究发现,600μm厚支架中的细胞增殖和肝细胞生长因子释放高于100μm厚的支架。将植入和未植入干细胞的支架皮下植入受体小鼠背部,进行体内研究,以测试其在0至3周内的生物降解性和生物相容性。接种在600μm厚支架上的细胞在体内促进了显著的新血管形成。3周后,大量供体细胞仅在600μm厚支架的内部持续存在。因此,使用更厚的基质可以延长干细胞在植入过程中分泌生长因子的作用时间。这些600μm厚的支架有可能用于通过干细胞共培养修复和再生损伤,实现植入物的血管化。