Hosseini Seyed Mojtaba, Vasaghi Attiyeh, Nakhlparvar Newsha, Roshanravan Reza, Talaei-Khozani Tahereh, Razi Zahra
Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran ; Cell and Molecular Medicine Student Research Group, Medical School, Shiraz University of Medical Sciences, Shiraz, Iran ; Stem Cell Laboratory, Department of Anatomy, Shiraz University of Medical Sciences, Shiraz, Iran.
Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran ; Cell and Molecular Medicine Student Research Group, Medical School, Shiraz University of Medical Sciences, Shiraz, Iran.
Neural Regen Res. 2015 Aug;10(8):1312-6. doi: 10.4103/1673-5374.162768.
Alginate scaffold has been considered as an appropriate biomaterial for promoting the differentiation of embryonic stem cells toward neuronal cell lineage. We hypothesized that alginate scaffold is suitable for culturing Wharton's jelly mesenchymal stem cells (WJMSCs) and can promote the differentiation of WJMSCs into neuron-like cells. In this study, we cultured WJMSCs in a three-dimensional scaffold fabricated by 0.25% alginate and 50 mM CaCl2 in the presence of neurogenic medium containing 10 μM retinoic acid and 20 ng/mL basic fibroblast growth factor. These cells were also cultured in conventional two-dimensional culture condition in the presence of neurogenic medium as controls. After 10 days, immunofluorescence staining was performed for detecting β-tubulin (marker for WJMSCs-differentiated neuron) and CD271 (motor neuron marker). β-Tubulin and CD271 expression levels were significantly greater in the WJMSCs cultured in the three-dimensional alginate scaffold than in the conventional two-dimensional culture condition. These findings suggest that three-dimensional alginate scaffold cell culture system can induce neuronal differentiation of WJMSCs effectively.
藻酸盐支架已被认为是一种合适的生物材料,可促进胚胎干细胞向神经细胞谱系分化。我们假设藻酸盐支架适合培养沃顿胶间充质干细胞(WJMSCs),并能促进WJMSCs分化为神经元样细胞。在本研究中,我们将WJMSCs培养在由0.25%藻酸盐和50 mM氯化钙制成的三维支架中,同时加入含有10 μM视黄酸和20 ng/mL碱性成纤维细胞生长因子的神经诱导培养基。作为对照,这些细胞也在神经诱导培养基存在的情况下,于传统二维培养条件下培养。10天后,进行免疫荧光染色以检测β-微管蛋白(WJMSCs分化神经元的标志物)和CD271(运动神经元标志物)。在三维藻酸盐支架中培养的WJMSCs中,β-微管蛋白和CD271的表达水平显著高于传统二维培养条件。这些发现表明,三维藻酸盐支架细胞培养系统可有效诱导WJMSCs的神经元分化。