一种优化的可注射水凝胶支架支持人牙髓干细胞的生存和扩散。

Advances in Medicine Pub Date : 2016-01-01 Epub Date: 2016-05-16 DOI:10.1155/2016/7363579
T D Jones, A Kefi, S Sun, M Cho, S B Alapati
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引用次数: 24

摘要

介绍。HyStem-C™是一种市售可注射水凝胶,由聚乙二醇二丙烯酸酯(PEGDA)、透明质酸(HA)和明胶(Gn)组成。这些成分可以通过机械调节来增强细胞活力和扩散。方法。添加二硫键的PEGDA (PEGSSDA)的浓度在0.5 ~ 8.0% (w/v)范围内变化,以确定临床注射应用的最佳浓度。我们评估了人牙髓干细胞(hDPSCs)包埋在2% (w/v) PEGSSDA-HA-Gn水凝胶中的细胞活力。HA: Gn的体积比从100:0到25:75变化,以促进hDPSC的扩散。在我们的模型中加入纤维连接蛋白(Fn),以确定细胞外基质蛋白浓度对hDPSC行为的影响。结果。我们的初步数据表明,随着PEGSSDA交联剂浓度的增加,水凝胶凝胶化时间缩短。PEGSSDA-HA-Gn与hdpsc具有生物相容性,增加HA: Gn的比例可提高细胞存活14天。此外,添加纤维连接蛋白的PEGDA-HA-Gn水凝胶在1.0和10.0 μg/mL浓度下,随着时间的推移,细胞增殖显著增加,而在0.1 μg/mL浓度下,细胞扩散显著增加。结论。本研究表明,以聚乙二醇为基础的可注射水凝胶主要在细胞外基质(ECM)蛋白存在的情况下维持hDPSC的活力并促进细胞扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

An Optimized Injectable Hydrogel Scaffold Supports Human Dental Pulp Stem Cell Viability and Spreading.

An Optimized Injectable Hydrogel Scaffold Supports Human Dental Pulp Stem Cell Viability and Spreading.

An Optimized Injectable Hydrogel Scaffold Supports Human Dental Pulp Stem Cell Viability and Spreading.

An Optimized Injectable Hydrogel Scaffold Supports Human Dental Pulp Stem Cell Viability and Spreading.

Introduction. HyStem-C™ is a commercially available injectable hydrogel composed of polyethylene glycol diacrylate (PEGDA), hyaluronan (HA), and gelatin (Gn). These components can be mechanically tuned to enhance cell viability and spreading. Methods. The concentration of PEGDA with an added disulfide bond (PEGSSDA) was varied from 0.5 to 8.0% (w/v) to determine the optimal concentration for injectable clinical application. We evaluated the cell viability of human dental pulp stem cells (hDPSCs) embedded in 2% (w/v) PEGSSDA-HA-Gn hydrogels. Volume ratios of HA : Gn from 100 : 0 to 25 : 75 were varied to encourage hDPSC spreading. Fibronectin (Fn) was added to our model to determine the effect of extracellular matrix protein concentration on hDPSC behavior. Results. Our preliminary data suggests that the hydrogel gelation time decreased as the PEGSSDA cross-linker concentration increased. The PEGSSDA-HA-Gn was biocompatible with hDPSCs, and increased ratios of HA : Gn enhanced cell viability for 14 days. Additionally, cell proliferation with added fibronectin increased significantly over time at concentrations of 1.0 and 10.0 μg/mL in PEGDA-HA-Gn hydrogels, while cell spreading significantly increased at Fn concentrations of 0.1 μg/mL. Conclusions. This study demonstrates that PEG-based injectable hydrogels maintain hDPSC viability and facilitate cell spreading, mainly in the presence of extracellular matrix (ECM) proteins.

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