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Long-Term Cryostorage of Mesenchymal Stem Cell-Containing Hybrid Hydrogel Scaffolds Based on Fibrin and Collagen

机译:基于纤维蛋白和胶原的间充质干细胞杂交水凝胶支架长期低温蒸发器

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摘要

The most difficult issue when using tissue engineering products is enabling the ability to store them without losing their restorative capacity. The numbers and viability of mesenchymal stem cells encapsulated in a hydrogel scaffold after cryostorage at −80 °C (by using, individually, two kinds of cryoprotectors—Bambanker and 10% DMSO (Dimethyl sulfoxide) solution) for 3, 6, 9, and 12 months were determined, with subsequent assessment of cell proliferation after 96 h. The analysis of the cellular component was performed using fluorescence microscopy and the two fluorochromes—Hoechst 3334 and NucGreenTM Dead 488. The experimental protocol ensured the preservation of cells in the scaffold structure, retaining both high viability and proliferative activity during storage for 3 months. Longer storage of scaffolds led to their significant changes. Therefore, after 6 months, the proliferative activity of cells decreased. Cryostorage of scaffolds for 9 months led to a decrease in cells’ viability and proliferative activity. As a result of cryostorage of scaffolds for 12 months, a decrease in viability and proliferative activity of cells was observed, as well as pronounced changes in the structure of the hydrogel. The described scaffold cryostorage protocol could become the basis for the development of storage protocols for such tissue engineering products, and for helping to extend the possibilities of their clinical use while accelerating their commercialization.
机译:使用组织工程产品时,最困难的问题是能够在不失去恢复能力的情况下储存它们。在-80℃的低温托晶段后封装在水凝胶支架中的间充质干细胞的数量和活力(通过使用,单独地,两种冷冻保护剂 - Bambanker和10%DMSO(二甲基磺氧化亚砜)溶液)进行3,6,9,和确定12个月,随后评估96小时后细胞增殖。使用荧光显微镜和两种荧光铬-Hoechst 3334和Nucgreentm死488进行细胞组分的分析。实验方案确保保存支架结构中的细胞,在储存期间保持高活力和增殖活性3个月。脚手架的较长储存导致了它们的显着变化。因此,在6个月后,细胞的增殖活性减少。支架的冷冻镜9个月导致细胞的活力和增殖活性降低。由于支架的低温蒸馏12个月,观察到细胞的活力和增殖活性的降低,以及水凝胶结构的显着变化。所描述的支架低温仪协议可以成为这种组织工程产品的储存协议开发的基础,并且有助于帮助延长其临床应用的可能性,同时加速其商业化。

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