Review Article
Electrical Stimulation Promotes Stem Cell Neural Differentiation in Tissue Engineering
Table 2
Direct current stimulation used in stem cell neural differentiation.
| ES type | Cell type | Conductive material | Stimulation parameters | ES effect | Reference |
| DC | NSCs | Two parallel Ag/AgCl wires | 115 V/m, 2 hours/day for two days | Enhanced undifferentiated cell mobility and directional migration, and differentiation towards βIII-tubulin+ neurons | Zhao H et al. [39] | DC | NSCs | Platinum electrodes | 0.53 or 1.83 V/m, 10 min/days for 2 days | Increased neurites length, and βIII-tubulin, NeuN gene expression and in intracellular Ca2+ | Kobelt LJ et al. [40] | DC | MSCs | Two parallel 316 L stainless steel electrodes, PANI films | 1 mV-2 V, 10 min/day, 3 days | Enhanced filopodial elongation, increased nestin and βIII-tubulin gene expression | Thrivikraman G et al. [41] | DC | NSCs | Poly-D-lysin/lamini-coated electrotactic chambers | 150 mV/mm, 7, 14 days | Enhanced neural differentiation (Ascl1, βIII-tubulin, MAP2 gene expression) | Dong ZY et al. [42] | DC | Coculture of C2C12 with hMSCs | Two parallel electrodes | 8 mV/mm, 20 h/day, 8 days | Increased neural markers (SOX2, nestin, βIII-tubulin) gene level and intracellular Ca2+ activity | Naskar S et al. [43] |
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