Institute of Polymer Science and Engineering, National Taiwan University, Taipei, Taiwan, ROC.
Biomaterials. 2012 Dec;33(35):8943-54. doi: 10.1016/j.biomaterials.2012.08.069. Epub 2012 Sep 15.
Mesenchymal stem cells (MSCs) were recently found to form three-dimensional (3D) multicellular spheroids on chitosan membranes. The exact mechanism of spheroid formation, however, remains unclear. In this study, the regulation of spheroid formation for adipose derived adult stem cells (ADAS) grown on chitosan membranes was examined. By varying the membrane thickness, calcium concentration in culture medium, and acetylation extent of chitosan, the physico-chemical characteristics of chitosan that modulated spheroid formation was elucidated. The capacity of cardiomyogenic differentiation was further evaluated. Results suggested that the calcium binding capacity of chitosan may affect the cell-substrate and cell-cell interactions and critically influence the dynamics of spheroid formation. The intracellular calcium level was elevated for ADAS spheroids on chitosan. Chitosan-bound calcium was observed to enter the cells. The expression of N-cadherin was upregulated for ADAS spheroids on chitosan, evidenced by quantitative RT-PCR and Western blot. After the induction by 5-aza, the expression levels of cardiac marker genes (Gata4, Nkx2.5, Tnnt2, and Myh6) were remarkably enhanced (about four-fold) for ADAS on chitosan vs. tissue culture polystyrene or polyvinyl alcohol. Immunofluorescence staining confirmed the expression of cardiac-associated tight junction protein ZO-1 for ADAS grown on chitosan membranes. The gene expression of Wnt11 was significantly upregulated for ADAS spheroids on chitosan at 3 days and 12 days. We suggested that Wnt11 may be involved in the spheroid formation and cardiomyogenic differentiation of MSCs on chitosan membranes. Spheroids formed on the acetylated chitosan or polyvinyl alcohol membranes failed to show such behavior. The properties of MSC spheroids were therefore determined by the culture substrate.
间充质干细胞(MSCs)最近被发现可在壳聚糖膜上形成三维(3D)多细胞球体。然而,球体形成的确切机制仍不清楚。在这项研究中,研究了在壳聚糖膜上生长的脂肪来源的成体干细胞(ADAS)球体形成的调节。通过改变膜的厚度、培养基中的钙离子浓度和壳聚糖的乙酰化程度,阐明了调节壳聚糖球体形成的物理化学特性。进一步评估了心肌生成分化的能力。结果表明,壳聚糖的钙结合能力可能影响细胞-基质和细胞-细胞相互作用,并对球体形成的动力学产生重大影响。ADAS 球体在壳聚糖上的细胞内钙离子水平升高。观察到壳聚糖结合的钙进入细胞。ADAS 球体在壳聚糖上的 N-钙粘蛋白表达上调,通过定量 RT-PCR 和 Western blot 证实。在用 5-aza 诱导后,ADAS 在壳聚糖上的心脏标记基因(Gata4、Nkx2.5、Tnnt2 和 Myh6)的表达水平显著增强(约四倍)相比,组织培养聚苯乙烯或聚乙烯醇。免疫荧光染色证实了 ADAS 在壳聚糖膜上的心脏相关紧密连接蛋白 ZO-1 的表达。ADAS 球体在壳聚糖上的 Wnt11 基因表达在第 3 天和第 12 天显著上调。我们认为 Wnt11 可能参与了 MSC 在壳聚糖膜上的球体形成和心肌生成分化。在乙酰化壳聚糖或聚乙烯醇膜上形成的球体未能表现出这种行为。因此,MSC 球体的性质取决于培养底物。