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磁致感应加热和微胶囊化的双重抑制作用可使干细胞-藻酸盐水凝胶构建体进行低浓度保护剂玻璃化。

Dual Suppression Effect of Magnetic Induction Heating and Microencapsulation on Ice Crystallization Enables Low-Cryoprotectant Vitrification of Stem Cell-Alginate Hydrogel Constructs.

机构信息

Department of Electronic Science and Technology , University of Science and Technology of China , Hefei 230027 , Anhui , China.

Fischell Department of Bioengineering , University of Maryland , College Park , Maryland 20742 , United States.

出版信息

ACS Appl Mater Interfaces. 2018 May 16;10(19):16822-16835. doi: 10.1021/acsami.8b04496. Epub 2018 May 7.

Abstract

Stem cells microencapsulated in hydrogel as stem cell-hydrogel constructs have wide applications in the burgeoning cell-based medicine. Due to their short shelf life at ambient temperature, long-term storage or banking of the constructs is essential to the "off-the-shelf" ready availability needed for their widespread applications. As a high-efficiency, easy-to-operate, low-toxicity, and low-cost method for long-term storage of the constructs, low-cryoprotectant (CPA) vitrification has attracted tremendous attention recently. However, we found many cells in the stem cell-alginate constructs (∼500 μm in diameter) could not attach to the substrate post low-CPA vitrification with ∼2 M penetrating CPAs. To address this problem, we introduced nanowarming via magnetic induction heating (MIH) of FeO nanoparticles to minimize recrystallization and devitrification during the warming step of the low-CPA vitrification procedure. Our results indicate that high-quality stem cell-alginate hydrogel constructs with an intact microstructure, high immediate cell survival (>80%), and greatly improved attachment efficiency (by nearly three times, 68% versus 24%) of the encapsulated cells could be obtained post-cryopreservation with nanowarming. Moreover, the cells encapsulated in the cell-hydrogel constructs post-cryopreservation maintained normal proliferation under 3D culture and retained intact biological function of multilineage differentiation. This novel low-CPA vitrification approach for cell cryopreservation enabled by the combined use of alginate hydrogel microencapsulation and FeO nanoparticles-mediated nanowarming may be valuable in facilitating the widespread application of stem cells in the clinic.

摘要

将干细胞微囊封在水凝胶中作为干细胞-水凝胶构建体,在新兴的基于细胞的医学中有广泛的应用。由于其在环境温度下的保质期短,因此对构建体进行长期储存或存储对于实现广泛应用所需的“即用型”现成可用性至关重要。作为一种高效、易于操作、低毒性和低成本的长期储存构建体的方法,低冷冻保护剂 (CPA) 玻璃化最近引起了极大的关注。然而,我们发现许多细胞在干细胞-藻酸盐构建体(直径约 500 μm)中不能附着在基质上,用约 2 M 的穿透性 CPA 进行低-CPA 玻璃化后。为了解决这个问题,我们通过 FeO 纳米粒子的磁感应加热 (MIH) 引入了纳米升温,以最大限度地减少低-CPA 玻璃化程序升温过程中的再结晶和非晶化。我们的结果表明,通过纳米升温,可以获得具有完整微观结构、高即时细胞存活率(>80%)和封装细胞附着效率大大提高(近三倍,68%对 24%)的高质量干细胞-藻酸盐水凝胶构建体。此外,在 3D 培养下,冷冻保存后细胞在细胞-水凝胶构建体中保持正常增殖,并保留多谱系分化的完整生物学功能。这种新型的低-CPA 细胞冷冻保存方法结合使用藻酸盐水凝胶微囊化和 FeO 纳米粒子介导的纳米升温,可能有助于干细胞在临床上的广泛应用。

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