Electrophysiological Properties of Mitogen-Expanded Adult Rat Spinal Cord and Subventricular Zone Neural Precursor Cells

• Published in: Experimental neurology 1999-07, Vol.158 (1), p.143-154
• Main Authors: Liu, Rong-Huan, Morassutti, Dante J., Whittemore, Scott R., Sosnowski, Jeffrey S., Magnuson, David S.K.
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; cell culture; Cell Differentiation - drug effects; Cells, Cultured; Central nervous system; Cerebral Ventricles - cytology; Cerebral Ventricles - drug effects; development; Electric Stimulation - methods; Electrophysiology; Epidermal Growth Factor - metabolism; Fibroblast Growth Factors - metabolism; Fundamental and applied biological sciences. Psychology; Glutamic Acid - pharmacology; Membrane Potentials - drug effects; Mitogens - pharmacology; neural precursor cell; Neuroglia - cytology; Neuroglia - drug effects; Neurons - cytology; Neurons - drug effects; progenitor cell; Rats; Rats, Sprague-Dawley; spinal cord; Spinal Cord - cytology; Spinal Cord - drug effects; Stem Cells - drug effects; subventricular zone; Time Factors; Vertebrates: nervous system and sense organs
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1006/exnr.1999.7078

Growth factor-expanded neural precursor cells isolated from the mammalian central nervous system can differentiate into neurons and glia. Although the morphological and neurochemical development of these neural precursor cells has been investigated, little attention has been paid to their electrophysiology. This study examined the electrophysiological properties of neurons and glia derived from neural precursor cells isolated from the adult rat spinal cord (SC) and subventricular zone (SVZ). Cells were cultured in medium containing epidermal growth factor and/or fibroblast growth factor-2. After at least two passages, spheres of neural precursor cells were plated on coated coverslips and maintained in culture for up to 6 weeks. Whole-cell patch recordings were made using standard current clamp techniques. Immature action potentials were observed within hours of plating for both SC and SVZ cells. Input resistance and time constants decreased over the first week after plating and no further changes were found at later times. At similar times following plating, however, SVZ cells had a lower input resistance and shorter time constant compared to SC cells. SVZ cells also had higher resting membrane potentials and smaller after hyperpolarizations than those of SC cells, despite no significant difference in the amplitude of action potentials. Neither the SC nor the SVZ cells were capable of eliciting more than a single action potential in response to injected current. While all SC cells tested were depolarized by glutamate, the response of SVZ cells to glutamate varied considerably. This study revealed that neural precursor cells from SC and SVZ differ in both active and passive membrane properties. It appears also that the electrophysiological development of SC and SVZ precursor-derived neurons is incomplete under the conditions used. These observations suggest that the neural precursor cells from different anatomical locations may be physiologically diverse and may exhibit some differences in commitment toward neuronal or glial phenotypes.