Abstract
Voltage-gated potassium (K) currents are important in controlling a neuron's excitability. We have shown previously (McFarlane and Cooper, 1992) that neonatal superior cervical ganglia (SCG) neurons express three voltage-gated K currents: a noninactivating delayed-rectifier type current (IK), a rapidly inactivating A-current (IAf), and a slowly inactivating A-current (IAs). When grown in culture for 4 weeks without other cell types, SCG neurons lose their expression of IAf and IAs, suggesting that an extrinsic factor(s) is involved in controlling the expression of these currents. In vivo, SCG neurons are surrounded by non-neuronal cells. Therefore, in this study we investigated whether the ganglionic non-neuronal cells provide a factor required for A- current expression. We show that postnatal day 1 (P1) SCG neurons continue to express IAf and IAs when cocultured with their ganglionic non-neuronal cells. Medium conditioned by ganglionic non-neuronal cells mimics the non-neuronal cell influence on IAf and IAs expression, suggesting that the effects of non-neuronal cells are mediated by way of a secreted factor. Ciliary neurotrophic factor, a factor present in peripheral non-neuronal cells, had similar effects to those of ganglionic cell-conditioned medium. Moreover, we find that the dependence of IAf on a non-neuronal cell factor is developmentally regulated; P14 neurons grown in culture without other cell types continue to express IAf. However, IAs on P14 neurons maintains its dependence on a factor from non-neuronal cells. Finally, in addition to extrinsic control of voltage-gated K currents, we suggest that SCG neurons use intrinsic mechanisms to coordinate their expression of IAf, IAs, and IK such that changes in one K current are compensated for by reciprocal changes in one or more of the other K currents.