Comparison of Pluripotency, Differentiation, and Mitochondrial Metabolism Capacity in Three-Dimensional Spheroid Formation of Dental Pulp-Derived Mesenchymal Stem Cells

• Published in: BioMed research international Vol. 2021; pp. 1 - 10
• Main Authors: Son, Young-Bum, Bharti, Dinesh, Kim, Saet-Byul, Jo, Chan-Hee, Bok, Eun-Yeong, Lee, Sung-Lim, Kang, Young-Hoon, Rho, Gyu-Jin
• Format: Journal Article
• Language: English
• Published: New York Hindawi 2021; Hindawi Limited
• Subjects: Agglomeration; Antibodies; Apoptosis; Biomedical materials; Biotechnology; Cell aggregation; Cell culture; Cell cycle; Cell growth; Culture techniques; Dental pulp; Differentiation; Flow cytometry; Glucose; Mesenchymal stem cells; Metabolism; Mitochondria; Monolayers; Oxygen consumption; Pluripotency; Spheroids; Stem cells; Tissue engineering; United States > US
• DOI: 10.1155/2021/5540877
• ISSN: 2314-6133

Mesenchymal stem cells (MSCs) are valuable candidates in tissue engineering and stem cell-based therapy. Traditionally, MSCs derived from various tissues have been successfully expanded in vitro using adherent culture plates commonly called as monolayer two-dimensional (2D) cultures. Recently, many studies demonstrated that stemness and multilineage differentiation potential could be enhanced to greater extent when MSCs are cultured as suspended aggregates by means of three-dimensional (3D) culturing techniques. However, there are limited reports on changed mitochondrial metabolism on 3D spheroid formation of MSCs. Therefore, the present study was aimed at investigating the stemness, differentiation potential, and mitochondrial metabolism capacity of 3D dental pulp-derived MSC (DPSC) spheroids in comparison to monolayer cultured DPSCs. We isolated dental pulp-derived MSCs (DPSCs) and successfully developed a 3D culture system which facilitated the formation of MSC spheroids. The cell aggregation was observed after 2 hours, and spheroids were formed after 24 hours and remained in shape for 72 hours. After spheroid formation, the levels of pluripotent markers increased along with enhancement in adipogenic and osteogenic potential compared to 2D cultured control cells. However, decreased proliferative capacity, cell cycle arrest, and elevated apoptosis rate were observed with the time course of the 3D culture except for the initial 24-hour aggregation. Furthermore, oxygen consumption rates of living cells decreased with the time course of the aggregation except for the initial 24 hours. Overall, our study indicated that the short-term 3D culture of MSCs could be a suitable alternative to culture the cells.