Center for Craniofacial and Molecular Biology, Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, CA, 90089, USA.
J Mater Sci Mater Med. 2012 Dec;23(12):3041-51. doi: 10.1007/s10856-012-4759-3. Epub 2012 Sep 4.
The objectives of this study were to: (1) develop an injectable and biodegradable scaffold based on oxidized alginate microbeads encapsulating periodontal ligament (PDLSCs) and gingival mesenchymal stem cells (GMSCs); and (2) investigate the stem cell viability, and osteogenic differentiation of the stem cells in vitro. Stem cells were encapsulated using alginate hydrogel. The stem cell viability, proliferation and differentiation to adipogenic and osteogenic tissues were studied. To investigate the expression of both adipogenesis and ontogenesis related genes, the RNA was extracted and RT-PCR was performed. The degradation behavior of hydrogel based on oxidized sodium alginate with different degrees of oxidation was studied in PBS at 37 °C as a function of time by monitoring the changes in weight loss. The swelling kinetics of alginate hydrogel was also investigated. The results showed that alginate is a promising candidate as a non-toxic scaffold for PDLSCs and GMSCs. It also has the ability to direct the differentiation of these stem cells to osteogenic and adipogenic tissues as compared to the control group in vitro. The encapsulated stem cells remained viable in vitro and both osteo-differentiated and adipo-differentiated after 4 weeks of culturing in the induction media. It was found that the degradation profile and swelling kinetics of alginate hydrogel strongly depends on the degree of oxidation showing its tunable chemistry and degradation rate. These findings demonstrate for the first time that immobilization of PDLSCs and GMSCs in the alginate microspheres provides a promising strategy for bone tissue engineering.
(1)开发一种基于氧化海藻酸钠微球包埋牙周膜(PDLSCs)和牙龈间充质干细胞(GMSCs)的可注射和可生物降解的支架;(2)研究体外干细胞的活力和向成骨细胞分化的情况。使用海藻酸钠水凝胶包封干细胞。研究了干细胞的活力、增殖和向脂肪和成骨组织的分化情况。为了研究脂肪生成和个体发生相关基因的表达,提取 RNA 并进行 RT-PCR。在 37°C 的 PBS 中,通过监测重量损失的变化,研究了不同氧化度的氧化钠海藻酸盐基水凝胶的降解行为。还研究了海藻酸盐水凝胶的溶胀动力学。结果表明,海藻酸盐作为 PDLSCs 和 GMSCs 的无毒支架具有很大的潜力。与对照组相比,它还具有在体外将这些干细胞定向分化为成骨细胞和脂肪细胞的能力。在诱导培养基中培养 4 周后,体外培养的包封干细胞仍然存活,并且都能向成骨细胞和脂肪细胞分化。研究发现,海藻酸盐水凝胶的降解曲线和溶胀动力学强烈依赖于氧化程度,表明其具有可调的化学性质和降解速率。这些发现首次证明,将 PDLSCs 和 GMSCs 固定在海藻酸钠微球中为骨组织工程提供了一种很有前途的策略。