组织工程用多糖类水凝胶

RAN Pub Date : 2016-04-01 DOI:10.11159/NDDTE16.112
Jaewon Lee, Hyoseok An, K. Lee
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引用次数: 3

摘要

多糖具有良好的生物相容性,是生物医学领域广泛应用的材料之一。然而,大多数基于多糖的水凝胶通常是在可能引起毒性的赋形化学试剂存在的情况下制备的。在本报告中,我们报告了如何制备透明质酸水凝胶,而不使用有毒的化学交联剂。透明质酸是由β-1,4- d-葡萄糖醛酸-β-1,3- n -乙酰- d-葡萄糖胺残基组成,在滑液和细胞外基质中含量丰富。我们将海藻酸盐引入透明质酸骨架,允许在钙离子存在下形成凝胶[1]。水凝胶的力学性能随多糖种类和浓度的不同而变化。利用这些水凝胶将原代软骨细胞/水凝胶构建物皮下注射到小鼠模型中进行组织再生。此外,利用水凝胶控制干细胞表型已被广泛研究,使用细胞指导聚合物对调节间充质干细胞(MSCs)的增殖和分化至关重要[2]。在本报告中,我们报告了一个仿生系统,通过使用细胞引导藻酸盐微球提供干细胞生态位来培养间充质干细胞。MSCs的成软骨分化通常受到聚集形成的影响[3],钙粘蛋白是干细胞凝聚和成软骨过程中介导细胞间相互作用的关键因子。采用油包水乳液法制备海藻酸盐微球,并在氯化钙存在下固化[4],用E-cadherin受体衍生的肽修饰海藻酸盐微球。肽修饰的海藻酸盐微球在MSCs存在下形成聚集体,导致良好的细胞活力,并促进体外软骨形成。这种方法可能会在三维干细胞培养和组织工程中找到有用的应用。
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Polysaccharide-Based Hydrogels for Tissue Engineering
Extended Abstract Polysaccharide is one of widely utilized materials in biomedical areas due to its excellent biocompatibility. However, most polysaccharide-based hydrogels are typically prepared in the presence of excipient chemical reagents that may cause toxicity. In this presentation, we report how hyaluronate hydrogels can be prepared without toxic chemical cross-linking agents. Hyaluronate is composed of β-1,4-D-glucuronic acid-β-1,3-N-acetyl-D-glucosamine residues, and is abundant in synovial fluid and extracellular matrix. We introduced alginate to the hyaluronate backbone, allowing gel formation in the presence of calcium ions [1]. The mechanical properties of hydrogels were varied depending on type and concentration of polysaccharide. Tissue regeneration using these hydrogels were carried out by subcutaneous injection of primary chondrocyte/hydrogel constructs into a mouse model. In addition, a control of stem cell phenotype using hydrogels has been extensively investigated, and a use of cellinstructive polymers is critical to regulate the proliferation and differentiation of mesenchymal stem cells (MSCs) [2]. In this presentation, we report a biomimetic system to culture MSCs by providing stem cell niche using cell-instructive alginate microspheres. Chondrogenic differentiation of MSCs is typically influenced by aggregate formation [3] and cadherin is a key factor in mediating cell-cell interactions during stem cell condensation and chondrogenesis. Alginate microspheres, prepared by the water-in-oil emulsion method and solidified in the presence of calcium chloride [4], were thus modified with a peptide derived from E-cadherin receptor. Peptide-modified alginate microspheres formed an aggregate in the presence of MSCs, resulted in excellent cell viability, and promoted chondrogenesis in vitro. This approach may find useful applications in 3-D stem cell culture and tissue engineering.
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