Department of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Department of Stem Cell Biology, Stem Cell Technology Research Center, Tehran, Iran.
Mater Sci Eng C Mater Biol Appl. 2021 Jan;120:111739. doi: 10.1016/j.msec.2020.111739. Epub 2020 Nov 21.
The cell-extracellular matrix (ECM) interactions are known to have a strong impact on cell behaviors in neural tissues. Due to complex physiology system and limited regenerative capacity of nervous system, neural tissue engineering has attracted attention as a promising strategy. In this study, we designed a hydrogel loaded by poly (lactic-co-glycolic acid) (PLGA) microspheres containing carbon nanotubes (CNT) and the biochemical differentiation factors, as a scaffold, in order to replicate the neural niche for stem cell growth (and/or differentiation). Different formulations from Hyaluronic acid (H), Poloxamer (P), Ethoxy-silane-capped poloxamer (PE), and cross-linked Alginate (Alg) were utilized as an in situ gel structure matrix to mirror the mechanical properties of the ECM of CNS. Subsequently, conductivity, surface morphology, size of microspheres, and CNT dispersion in microsphere were measured using two probes electrical conductometer, scanning electron microscopy (SEM), dynamic light scattering (DLS), and Raman spectroscopy, respectively. According to SEM and fluorescent microscopy images, CNTs increased the porosity of polymeric structure, which, in turn, facilitated the adhesion of stem cells on the surface of microspheres compared with control. Microstructure and rheological behaviors of different gel compositions were investigated using SEM and parallel-plate oscillatory rheometer, respectively. The MTT assay showed the toxicity profile of hydrogels was appropriate for cell transplantation. The confocal images illustrated the 3D platform of P15%H10% and P20%H5% gel formulations containing the PLGA-CNT microspheres, which allows the proliferation of neural stem cells (NSCs) derived from MSC. The results of real-time PCR and immunocytochemistry showed neuronal differentiation capacity of cultured NSCs derived from MSC in the alginate gel that contained PLGA-CNT microspheres as well as other control groups. The dispersion of the CNT-PLGA microspheres, covered by NSCs, into alginate gel in the presence of induction factors was found to notably enhance the expression of Sox2-SYP and β-Tubulin III neuronal markers.
细胞-细胞外基质(ECM)的相互作用被认为对神经组织中的细胞行为有很强的影响。由于神经系统的复杂生理系统和有限的再生能力,神经组织工程作为一种有前途的策略引起了人们的关注。在这项研究中,我们设计了一种水凝胶,其中负载了含有碳纳米管(CNT)和生化分化因子的聚(乳酸-共-乙醇酸)(PLGA)微球,作为支架,以复制干细胞生长(和/或分化)的神经龛。不同配方的透明质酸(H)、泊洛沙姆(P)、乙氧基-硅烷封端的泊洛沙姆(PE)和交联海藻酸盐(Alg)被用作原位凝胶结构基质,以模拟中枢神经系统 ECM 的机械性能。随后,使用双探针电导率计、扫描电子显微镜(SEM)、动态光散射(DLS)和拉曼光谱分别测量微球的导电性、表面形貌、微球的大小和 CNT 在微球中的分散性。根据 SEM 和荧光显微镜图像,与对照组相比,CNT 增加了聚合物结构的孔隙率,从而促进了干细胞在微球表面的黏附。使用 SEM 和平行板振荡流变仪分别研究了不同凝胶组成的微观结构和流变行为。MTT 测定表明水凝胶的毒性谱适合细胞移植。共聚焦图像说明了包含 PLGA-CNT 微球的 P15%H10%和 P20%H5%凝胶配方的 3D 平台,允许 MSC 来源的神经干细胞(NSCs)增殖。实时 PCR 和免疫细胞化学的结果表明,含有 PLGA-CNT 微球的藻酸盐凝胶中 MSC 来源的 NSCs 具有神经元分化能力,以及其他对照组。在诱导因子存在下,被 NSCs 覆盖的 CNT-PLGA 微球在藻酸盐凝胶中的分散明显增强了 Sox2-SYP 和 β-Tubulin III 神经元标记物的表达。