Department of Marine Bio-Pharmacology, College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China.
Department of Mechanical Engineering, McMaster University, Canada; School of Biomedical Engineering, McMaster University, Canada.
Int J Biol Macromol. 2020 Nov 15;163:9-18. doi: 10.1016/j.ijbiomac.2020.06.173. Epub 2020 Jun 20.
Fabrication of biomaterial that mimics a suitable biological microenvironment is still a major challenge in the field of periodontitis treatment. Hence, in this report, we presented for the first time the fabrication of a novel biomaterial 3D matrix using collagen combined with sodium alginate and titanium oxide (TiO) to recreate the in-vivo microenvironment and to act as a platform for the culture of human periodontal ligament fibroblasts (HPLF) towards osteogenic differentiation. Further, we explored the changes of differentiated and undifferentiated HPLF cells in morphological and cellular level comparing 2D (standard culture plates) and 3D cell culture systems. The physicochemical parameters such as stiffness, water binding capacity, swelling, shrinkage factor, porosity and in-vitro biodegradation show the suitability of this 3D matrix to act as a scaffold for in-vitro periodontal regeneration. The differentiated HPLF cells in the 3D matrix secrete high levels of collagen, osteocalcin, alkaline phosphatase compared to the conventional 2D cell culture. Morphological analysis revealed the structural changes of HPLF cells before and after differentiation in 2D and 3D cell culture. In this study, we find that the level of osteocalcin secretion towards osteogenic differentiation was enhanced in HPLF cells by 3D matrix as compared with 2D cell culture, which demonstrates the osteogenic stimulatory potential of 3D matrix. Overall, the fabricated 3D matrix supports the differentiation of the HPLF cells into osteoblastogenic lineage cells in-vitro and is a promising approach for further investigations in in-vivo treatment of periodontal tissue impairment.
生物材料的制造模仿合适的生物微环境仍然是牙周病治疗领域的主要挑战。因此,在本报告中,我们首次提出了使用胶原蛋白结合海藻酸钠和氧化钛(TiO)制造新型生物材料 3D 基质的方法,以重现体内微环境,并作为培养人牙周韧带成纤维细胞(HPLF)向成骨分化的平台。此外,我们通过比较 2D(标准培养板)和 3D 细胞培养系统,在形态和细胞水平上探索了分化和未分化的 HPLF 细胞的变化。物理化学参数,如硬度、水结合能力、溶胀、收缩因子、孔隙率和体外生物降解,表明这种 3D 基质适合作为体外牙周再生的支架。与传统的 2D 细胞培养相比,3D 基质中的分化 HPLF 细胞分泌高水平的胶原蛋白、骨钙素和碱性磷酸酶。形态分析显示了 HPLF 细胞在 2D 和 3D 细胞培养前后的结构变化。在这项研究中,我们发现 3D 基质可增强 HPLF 细胞向成骨分化的骨钙素分泌水平,与 2D 细胞培养相比,这表明 3D 基质具有成骨刺激潜力。总的来说,所制造的 3D 基质支持 HPLF 细胞在体外向成骨细胞谱系细胞分化,是进一步研究牙周组织损伤体内治疗的有前途的方法。