一种用于牙周韧带干细胞的新型水凝胶支架。

Krisztina Nagy, Orsolya Láng, Júlia Láng, Katalin Perczel-Kovách, Szabolcs Gyulai-Gaál, Kristóf Kádár, László Kőhidai, Gábor Varga
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引用次数: 21

摘要

牙周韧带干细胞(PDLSCs)具有广泛的再生潜力。然而,它们的治疗应用需要具有适当性能的支架。HydroMatrix (HydM)是近年来开发的一种新型可注射肽纳米纤维水凝胶。我们的目的是测试HydM是否可以作为PDLSCs增殖和成骨分化的合适支架。将PDLSCs植入未包被或hydm包被的表面。实时阻抗分析和细胞活力分析都记录了HydM上细胞的生长情况。PDLSCs在水凝胶上呈现健康的成纤维细胞样形态。在成骨培养基中培养3周后,与对照组相比,HydM培养物的矿化程度要高得多。在凝胶上生长的细胞的碱性磷酸酶活性达到未包被的对照水平。我们的数据提供了证据,证明PDLSCs可以在HydM上粘附、存活、迁移和增殖,并且这种凝胶也支持它们的成骨分化。我们首先将阻抗法应用于支架上培养的牙干细胞。HydM是PDLSCs体外研究的理想选择。它不仅可以作为参考材料,而且在未来作为一种有前途的生物相容性支架用于临床前研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A novel hydrogel scaffold for periodontal ligament stem cells.

Periodontal ligament stem cells (PDLSCs) possess extensive regeneration potential. However, their therapeutic application demands a scaffold with appropriate properties. HydroMatrix (HydM) is a novel injectable peptide nanofiber hydrogel developed recently for cell culture. Our aim was to test whether HydM would be a suitable scaffold for proliferation and osteogenic differentiation of PDLSCs. PDLSCs were seeded on non-coated or HydM-coated surfaces. Both real-time impedance analysis and cell viability assay documented cell growth on HydM. PDLSCs showed healthy, fibroblast-like morphology on the hydrogel. After a 3-week-long culture in osteogenic medium, mineralization was much more intense in HydM cultures compared to control. Alkaline phosphatase activity of the cells grown on the gels reached the non-coated control levels. Our data provided evidence that PDLSCs can adhere, survive, migrate, and proliferate on HydM and this gel also supports their osteogenic differentiation. We first applied impedimetry for dental stem cells cultured on a scaffold. HydM is ideal for in vitro studies of PDLSCs. It may also serve not only as a reference material but also in the future as a promising biocompatible scaffold for preclinical studies.

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来源期刊
Interventional Medicine and Applied Science
Interventional Medicine and Applied Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
15 weeks
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