Juriga David, Kalman Eszter Eva, Toth Krisztina, Barczikai Dora, Szöllősi David, Földes Anna, Varga Gabor, Zrinyi Miklos, Jedlovszky-Hajdu Angela, Nagy Krisztina S
Department of Biophysics and Radiation Biology, Semmelweis University, H-1089 Budapest, Hungary.
Department of Molecular Biology, Semmelweis University, H-1083 Budapest, Hungary.
Gels. 2022 Jan 18;8(2):65. doi: 10.3390/gels8020065.
Several types of promising cell-based therapies for tissue regeneration have been developing worldwide. However, for successful therapeutical application of cells in this field, appropriate scaffolds are also required. Recently, the research for suitable scaffolds has been focusing on polymer hydrogels due to their similarity to the extracellular matrix. The main limitation regarding amino acid-based hydrogels is their difficult and expensive preparation, which can be avoided by using poly(aspartamide) (PASP)-based hydrogels. PASP-based materials can be chemically modified with various bioactive molecules for the final application purpose. In this study, dopamine containing PASP-based scaffolds is investigated, since dopamine influences several cell biological processes, such as adhesion, migration, proliferation, and differentiation, according to the literature. Periodontal ligament cells (PDLCs) of neuroectodermal origin and SH-SY5Y neuroblastoma cell line were used for the in vitro experiments. The chemical structure of the polymers and hydrogels was proved by H-NMR and FTIR spectroscopy. Scanning electron microscopical (SEM) images confirmed the suitable pore size range of the hydrogels for cell migration. Cell viability assay was carried out according to a standardized protocol using the WST-1 reagent. To visualize three-dimensional cell distribution in the hydrogel matrix, two-photon microscopy was used. According to our results, dopamine containing PASP gels can facilitate vertical cell penetration from the top of the hydrogel in the depth of around 4 cell layers (~150 μm). To quantify these observations, a detailed image analysis process was developed and firstly introduced in this paper.
全球范围内正在研发几种用于组织再生的、前景广阔的基于细胞的疗法。然而,要在该领域成功地将细胞用于治疗,还需要合适的支架。近来,由于聚合物水凝胶与细胞外基质相似,对合适支架的研究一直聚焦于聚合物水凝胶。基于氨基酸的水凝胶的主要局限在于其制备困难且成本高昂,而使用基于聚(天冬酰胺)(PASP)的水凝胶可以避免这一问题。基于PASP的材料可以用各种生物活性分子进行化学修饰,以用于最终的应用目的。在本研究中,对含多巴胺的基于PASP的支架进行了研究,因为据文献报道,多巴胺会影响多种细胞生物学过程,如黏附、迁移、增殖和分化。神经外胚层来源的牙周膜细胞(PDLCs)和SH-SY5Y神经母细胞瘤细胞系被用于体外实验。通过H-NMR和FTIR光谱证实了聚合物和水凝胶的化学结构。扫描电子显微镜(SEM)图像证实了水凝胶具有适合细胞迁移的孔径范围。使用WST-1试剂按照标准化方案进行细胞活力测定。为了观察水凝胶基质中细胞的三维分布,使用了双光子显微镜。根据我们的结果,含多巴胺的PASP凝胶可以促进细胞从水凝胶顶部垂直穿透至约4个细胞层深度(约150μm)。为了量化这些观察结果,本文开发并首次引入了详细的图像分析流程。