Porous microscaffolds for 3D culture of dental pulp mesenchymal stem cells

• Published in: International journal of pharmaceutics 2016-12, Vol.515 (1-2), p.555-564
• Main Authors: Bhuptani, Ronak S., Patravale, Vandana B.
• Format: Article
• Language: English
• Subjects: 3D culture; Cell Culture Techniques - methods; Dental Pulp - cytology; Dental Pulp - metabolism; Dental Pulp - physiology; Dental pulp stem cell; Gene Expression Profiling; Humans; Lactic Acid; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - metabolism; Mesenchymal Stromal Cells - physiology; Microcarriers; Microscaffolds; PLGA; Polyglycolic Acid; Scaffolds; Stem cells; Tissue Scaffolds
• ISSN: 0378-5173; 1873-3476
• DOI: 10.1016/j.ijpharm.2016.10.040

[Display omitted] The collective power of stem cells due to their evident advantages is incessantly investigated in regenerative medicine to be the next generation exceptional remedy for tissue regeneration and treatment of diseases. Stem cells are highly sensitive and a 3D culture environment is a requisite for its successful transplantation and integration with tissues. Porous microscaffolds can create a 3D microenvironment for growing stems cells, controlling their fate both in vitro and in vivo. In the present study, interconnected porous PLGA microscaffolds were fabricated, characterized and employed to propagate human dental pulp mesenchymal stem cells (DPMSCs) in vitro. The porous topography was investigated by scanning electron microscopy and the pore size was controlled by fabrication conditions such as the concentration of porogen. DPMSCs were cultured on microscaffolds and were evaluated for their morphology, attachment, proliferation, cell viability via MTT and molecular expression (RT-PCR). DPMSCs were adequately proliferated and adhered over the microscaffolds forming a 3D cell-microscaffold construct. The average number of DPMSCs grown on PLGA microscaffolds was significantly higher than monolayer 2D culture during 5th and 7th day. Moreover, cell viability and gene expression results together corroborated that microscaffolds maintained the viability, stemness and plasticity of the cultured dental pulp mesenchymal stem cells. The novel porous microscaffold developed acts as promising scaffold for 3D culture and survival and transplantation of stem cells for tissue engineering.