New therapies are desperately needed for human central nervous system (CNS) regeneration to circumvent the lack of innate regenerative ability following traumatic injuries. Previously attempted therapies have been stymied by barriers to CNS regeneration largely because of protective mechanisms such as the blood brain barrier, inhibitory molecules, and glial scar formation. The application of electric stimulation (ES) has shown promise for enhancing peripheral nervous system regeneration, but is in its infancy in CNS regeneration. The objective of this study is to better understand how short duration ES can be harnessed to direct adult neural stem progenitor cell (NSPC) neurogenesis, neurite extension, and maturation. Herein, NSPCs were exposed to physiological levels of electrical stimulation of 0.53 or 1.83 V/m (applied power supply setting of 1.2 and 2.5 V) of direct current (DC) for 10 min/days for 2 days with a total differentiation time of 3 days. Culturing conditions consisted of either mitogenic growth factors or the neuronal differentiation factor interferon-γ (IFN-γ). Stimulated NSPCs showed lengths that were over five times longer than unstimulated controls (112.0 ± 88.8 μm at 0.53 V/m vs. 21.3 ± 8.5 μm for 0 V/m with IFN-γ) with the longest neurites reaching up to 600 µm. Additionally, ES resulted in mature neuronal morphologies and signs of differentiation through positive βIII tubulin, neuronal nuclei (NeuN), and better organized filamentous-actin (f-actin) staining with growth cone formation. Additionally, the neurites and soma of stimulated NSPCs showed increases in intracellular Ca(2+) during stimulation, signifying the presence of functional neurons capable of electrical conductance and communication with other cells. Our study demonstrates that short stimulation times (10 min/ day) result in significant neurite extension of stem cells in a quick time frame (3 days). This ES modality is potentially advantageous for promoting axon re-growth at an injury site using delivered adult stem cells; however, significant work still remains to understand both the delivery approach of cells as well as ES application in vivo.

New developments in growth factor and pharmaceutical control of cells for neural regenerative strategies have built a need for high throughput assays to conveniently screen these treatments in vitro before moving to more complex experiments. Towards this application, we have studied an easy and highly reproducible culture regime with a renewable cell source for central nervous system (CNS) strategies. Adult neural stem cells (NSCs) derived from the CNS are attractive for use in screening assay because they are easily expanded and can differentiate into all major CNS cell types. NSCs were cultured on glass alone or methacrylamide chitosan (MAC) hydrogel coated glass substrates, immobilized with extracellular matrix (ECM) proteins collagen and laminin at varying densities. Proteins were also adsorbed on the surfaces as a control. We found that adsorbed protein on hydrogel coated glass resulted in the highest cell densities after 8 d, over twice the density of immobilized groups or adsorbed protein on glass. No significant differences were observed between collagen, laminin, or both proteins together regarding cell differentiation (p > 0.05); however, the morphological spreading and branching of differentiated NSC processes was enhanced on MAC substrates with covalently immobilized laminin protein. The results of this study suggest that a soft MAC hydrogel surface with adsorbed protein would be most desirable for specifying neuronal differentiation of large numbers of stem cells due to the high cellularities they supported.

New developments in growth factor and pharmaceutical control of cells for neural regenerative strategies have built a need for high throughput assays to conveniently screen these treatments in vitro before moving to more complex experiments. Towards this application, we have studied an easy and highly reproducible culture regime with a renewable cell source for central nervous system (CNS) strategies. Adult neural stem cells (NSCs) derived from the CNS are attractive for use in screening assay because they are easily expanded and can differentiate into all major CNS cell types. NSCs were cultured on glass alone or methacrylamide chitosan (MAC) hydrogel coated glass substrates, immobilized with extracellular matrix (ECM) proteins collagen and laminin at varying densities. Proteins were also adsorbed on the surfaces as a control. We found that adsorbed protein on hydrogel coated glass resulted in the highest cell densities after 8 d, over twice the density of immobilized groups or adsorbed protein on glass. No significant differences were observed between collagen, laminin, or both proteins together regarding cell differentiation (p > 0.05); however, the morphological spreading and branching of differentiated NSC processes was enhanced on MAC substrates with covalently immobilized laminin protein. The results of this study suggest that a soft MAC hydrogel surface with adsorbed protein would be most desirable for specifying neuronal differentiation of large numbers of stem cells due to the high cellularities they supported.