Development of Transient Outward Currents Coupled With Ca2+-Induced Ca2+Release Mediates Oscillatory Membrane Potential in Ascidian Muscle Cells

Abstract

Isolated ascidian Halocynthia roretzi blastomeres of the muscle lineage exhibit muscle cell-like excitability on differentiation despite the arrest of cell cleavage early in development. This characteristic provides a unique opportunity to track changes in ion channel expression during muscle cell differentiation. Here, we show that the intrinsic membrane property of ascidian cleavage-arrested muscle-type cells becomes oscillatory by expressing transient outward currents ( Ito) activated by Ca2+-induced Ca2+release (CICR) in a maturation-dependent manner. In current-clamp mode, most day 4 (72 h after fertilization) cleavage-arrested muscle cells exhibited an oscillatory membrane potential of –20 mV at 15 Hz, whereas most day 3 (48 h after fertilization) cells exhibited a spiking pattern. In voltage-clamp mode, the day 4 cells exhibited prominent transient outward currents that were not present in day 3 cells. Itowas abolished by the application of 10 mM caffeine, implying that CICR was involved in Itoactivation. Itowas based on K+efflux and sensitive to tetraethylammonium and some Ca2+-activated K+channel inhibitors. We found a 60-pS single channel conductance that was activated by local Ca2+release in ascidian muscle cell. Voltage-clamp recording with an oscillatory waveform as a command pulse showed that CICR-activated K+currents were activated during the falling phase of the membrane potential oscillation. These results suggest that developmental expression of CICR-activated K+current plays a role in the maturation of larval locomotion by modifying the intrinsic membrane excitability of muscle cells.