N1E-115 mouse
neuroblastoma cells were injected with the
calcium indicator dye arsenazo III. Optical absorbance changes during voltage-clamp depolarization were used to examine the properties of the two
calcium currents present in these cells. The rapidly inactivating
calcium current (Moolenar and Spector, 1979b, Journal of Physiology, 292:307-323) inactivates by a voltage-dependent mechanism. The slowly inactivating
calcium current is dominant in raising intracellular
calcium during depolarizations to greater than -20 mV. Lowering the extracellular
calcium concentration affects the two
calcium currents unequally, with the slowly inactivating current being reduced more. Intracellular
calcium falls very slowly (tau greater than 1 min) after a depolarization. The rapidly inactivating
calcium current is responsible for a
calcium action potential under physiological conditions. In contrast, it is unlikely that the slowly inactivating
calcium current has an important electrical role. Rather, its function may be to add a further increment of
calcium influx over and above the
calcium influx through the rapidly inactivating
calcium channels.