Gaitán-Salvatella Iñigo, González-Alva Patricia, Montesinos Juan José, Alvarez-Perez Marco Antonio
Tissue Bioengineering Laboratory, Postgraduate Studies, Research Division, Faculty of Dentistry, National Autonomous University of Mexico (UNAM), Coyoacán, Mexico City 04510, Mexico.
Mesenchymal Stem Cells Laboratory, Oncology Research Unit, Oncology Hospital, National Medical Center (IMSS), POST, Mexico City 06720, Mexico.
Bioengineering (Basel). 2023 May 10;10(5):571. doi: 10.3390/bioengineering10050571.
Bone defects lead to the structural loss of normal architecture, and those in the field of bone tissue engineering are searching for new alternatives to aid bone regeneration. Dental pulp-mesenchymal stem cells (DP-MSC) could provide a promising alternative to repair bone defects, principally due to their multipotency and capacity to fabricate three-dimensional (3D) spheroids. The present study aimed to characterize the 3D DP-MSC microsphere and the osteogenic differentiation capacity potential cultured by a magnetic levitation system. To achieve this, the 3D DP-MSC microsphere was grown for 7, 14, and 21 days in an osteoinductive medium and compared to 3D human fetal osteoblast (hFOB) microspheres by examining the morphology, proliferation, osteogenesis, and colonization onto PLA fiber spun membrane. Our results showed good cell viability for both 3D microspheres with an average diameter of 350 μm. The osteogenesis examination of the 3D DP-MSC microsphere revealed the lineage commitment, such as the hFOB microsphere, as evidenced by ALP activity, the calcium content, and the expression of osteoblastic markers. Finally, the evaluation of the surface colonization exhibited similar patterns of cell-spreading over the fibrillar membrane. Our study demonstrated the feasibility of forming a 3D DP-MSC microsphere structure and the cell-behavior response as a strategy for the applications of bone tissue guiding.
骨缺损会导致正常结构的丧失,骨组织工程领域的研究人员正在寻找新的方法来促进骨再生。牙髓间充质干细胞(DP-MSC)有望成为修复骨缺损的替代方法,主要是因为它们具有多能性以及能够形成三维(3D)球体。本研究旨在表征3D DP-MSC微球体以及通过磁悬浮系统培养的成骨分化潜能。为此,将3D DP-MSC微球体在成骨诱导培养基中培养7天、14天和21天,并通过观察其形态、增殖、成骨情况以及在聚乳酸(PLA)纤维纺丝膜上的定植情况,与3D人胎儿成骨细胞(hFOB)微球体进行比较。我们的结果显示,两种平均直径为350μm的3D微球体均具有良好的细胞活力。对3D DP-MSC微球体的成骨检查显示,其细胞谱系定向与hFOB微球体相似,碱性磷酸酶活性、钙含量和成骨细胞标志物的表达均证明了这一点。最后,对表面定植的评估显示,细胞在纤维状膜上的铺展模式相似。我们的研究证明了形成3D DP-MSC微球体结构的可行性以及细胞行为反应作为骨组织引导应用策略的可行性。