Human Dental Pulp-Derived Mesenchymal Stem Cell Potential to Differentiate into Smooth Muscle-Like Cells In Vitro

• Published in: BioMed research international Vol. 2021; pp. 8858412 - 13
• Main Authors: Ha, Jinhee, Bharti, Dinesh, Kang, Young-Hoon, Lee, Sang-Yeob, Oh, Seong-Ju, Kim, Saet-Byul, Jo, Chan-Hee, Son, Jang-Ho, Sung, Iel-Yong, Cho, Yeong-Cheol, Rho, Gyu-Jin, Park, Jeong-Kil
• Format: Journal Article
• Language: English
• Published: United States Hindawi 2021; Hindawi Limited
• Subjects: Biomarkers; Biomedical materials; Cell culture; Cell differentiation; Cell surface; Cytokines; Dental pulp; Differentiation (biology); Gelatin; Medical research; Mesenchymal stem cells; Morphology; mRNA; Muscle contraction; Muscles; Platelet-derived growth factor; Platelet-derived growth factor BB; Plates; Pluripotency; Smooth muscle; Stem cells; Substrates; Surface markers; Transforming growth factor-b1; Denmark; United States > US; Japan
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2021/8858412

Previous studies have shown that mesenchymal stem cells (MSCs) derived from various tissue sources can be differentiated into smooth muscle-like cells (SMLCs) in vitro. In this paper, dental pulp-derived mesenchymal stem cells (DPSCs) were evaluated for their differentiation ability towards smooth muscle-like cells (SMLCs) under the effect of widely used cytokines (TGF-β1 and PDGF-BB) with special focus on different culturing environments. For this purpose, both the commercially used culturing plates (Norm-c) and 0.1% gelatin-precoated (Gel-c) plates were used. Isolated cells displayed plastic adherence, pluripotency and cell surface marker profiling, and adipogenic and osteogenic differentiation potential with lineage specific marker expression. Differentiated cells induced under different culturing plates showed successful differentiation into SMLCs by positively expressing smooth muscle cell (SMC) specific markers both at the mRNA and protein levels. Gelatin coating could substantially enhance DPSC differentiation potential than Norm-c-induced cells. However, the absence of mature marker MHY-11 by immunostaining results from all treatment groups further indicated the development of immature and synthetic SMLCs. Finally, it was concluded that DPSC differentiation ability into SMLCs can be enhanced under cytokine treatment as well as by altering the cellular niche by precoating the culturing plates with suitable substrates. However, to get fully functional, contractile, and mature SMLCs, still many different cytokine cocktail combinations and more suitable coating substrates will be needed.