Electrical Stimulation Decreases Dental Pulp Stem Cell Osteo-/Odontogenic Differentiation.
Karla Mychellyne Costa Oliveira1, Liudmila Leppik1, Khyati Keswani1
1Frankfurt Initiative for Regenerative Medicine, J.W. Goethe-University, Frankfurt/Main, Germany.
Electrical stimulation (EStim) did not enhance osteo-/odontogenic differentiation in dental pulp stem cells (DPSCs). Moderate EStim impaired cell function and differentiation, suggesting it may hinder tissue engineering applications.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Cell Biology
Background:
- Dental pulp stem cells (DPSCs) are crucial for tissue engineering (TE) in dentistry.
- Electrical stimulation (EStim) influences cellular functions relevant to TE.
- The impact of EStim on DPSCs remains under-investigated.
Purpose of the Study:
- To investigate the effects of direct current (DC) EStim on osteo-/odontogenic differentiation of DPSCs.
- To determine optimal EStim parameters for DPSC-based TE treatments.
Main Methods:
- DPSCs were isolated and characterized for stemness.
- Cells were exposed to varying voltages of DC EStim (10-150 mV/mm) for 7 days.
- Osteo-/odontogenic differentiation was assessed via calcium and collagen deposition, ALP activity, and gene expression (Osteocalcin, RunX2, BSP, DMP1).
Main Results:
- 10 and 50 mV/mm EStim had no effect on cell number or metabolic activity.
- 100 mV/mm EStim reduced cell number; 150 mV/mm caused cell death.
- Despite increased osteo-/odontogenic gene expression, 50 mV/mm EStim decreased collagen deposition and ALP activity, with reduced calcium deposition at day 14.
Conclusions:
- DC EStim, under the tested conditions, appears to impair DPSC osteo-/odontogenic differentiation.
- Further research is needed to understand DPSC responses to EStim for potential TE applications.
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