Effects of Y-27632 on the osteogenic and adipogenic potential of human dental pulp stem cells in vitro

• Published in: Human & experimental toxicology Vol. 41; p. 9603271221089003
• Main Authors: Xie, Zhiwei, Xu, Qiuping, Sun, Lu, Li, Ruijing, Shi, Jizhou, Yang, Qian, Zong, Min, Qin, Jianyong
• Format: Journal Article
• Language: English
• Published: London, England SAGE Publications 01.01.2022; Sage Publications Ltd
• Subjects: Adipogenesis; Alizarin; Alkaline phosphatase; Amides; Annexin V; Apoptosis; CD105 antigen; CD73 antigen; Cell Differentiation; Cell Proliferation; Cells, Cultured; Cholecystokinin; Cloning; Dental Pulp; Differentiation (biology); Gene expression; Genes; Humans; Lipids; Mesenchymal stem cells; Neural crest; NF-κB protein; Nodules; Osteogenesis; Phenotypes; Pyridines; Regenerative medicine; Staining; Stem Cells; Tissue engineering; TLR4 protein; Toll-like receptors; Human dental pulp stem cells; Y-27632 treatment; cell proliferation; adipogenic differentiation; osteogenic differentiation
• ISSN: 0960-3271; 1477-0903
• DOI: 10.1177/09603271221089003

Background Human dental pulp stem cells (hDPSCs) possess mesenchymal stem cell properties, originating from migrating neural crest cells. hDPSCs have received extensive attention in the field of tissue engineering and regenerative medicine due to their accessibility and ability to differentiate in several cell phenotypes. In this study, we cultured hDPSCs with Y-27632 to observe their biological behaviors changes. Methods The hDPSCs were separately cultured with Y-27632 (0, 0.156, 0.312, 0.625, 1.25, 2.50, 5, 10, 20, 40 μm) for 24, 48, 72 h to select the suitable concentration and time using CCK-8. Then, the hDPSCs were cultured with 2.50 μm Y-27632 for 48 h to analyzed the biological behaviors changes by 5-Ethynyl-2′-deoxyuridine (EdU), plate cloning, transwell, scratch, and Annexin V FITC/PI assays, separately. Additionally, osteogenic calcium nodules and lipid droplets were analyzed using alizarin red staining and oil red O staining, respectively. qRT-PCR was used to analyze the expression of osteogenesis, adipogenesis, stemness maintenance, and inflammation related genes. Results The hDPSCs proliferation was significantly enhanced after cultured with 2.50 μm Y-27632 for 48 h, but there was no significant difference in migration and apoptosis. Observation of alkaline phosphatase (ALP) activity, osteogenic and adipogenic differentiation abilities of hDPSCs, Y-27632 treatment clearly decreased the ALP activity and osteogenic differentiation ability, increased the adipogenic differentiation ability. Furthermore, Y-27632 decreased the CD73, CD90, CD105, CD166, TLR4, and NF-κB p65 genes expression, but increased the IL-8 gene expression. Conclusions The biological behaviors of hDPSCs could be changed when they cultured with Y-27632.