Kinetics of calcium steps underlying calcium oscillations in melanotrope cells of Xenopus laevis

Melanotrope cells of Xenopus laevis display intracellular calcium oscillations which are generated at the plasma membrane and travel as a wave through the cytoplasm into the nucleus. An oscillation involves discrete increases in intracellular Ca 2+ (‘steps’), followed by a relatively smooth return to the basal Cat 2+ level. The aim of our investigation was to determine what role these steps play in shaping the Ca 2+ signal in melanotrope cells, by conducting a high resolution spatio-temporal analysis of the kinetics of the Ca 2+ steps. To this end Fura-red loaded cells were analysed by confocal laser scanning microscopy using the line scanning method to achieve 6 ms time resolution. Furthermore, the kinetics of the steps were analysed in 3 different intracellular areas, to see if there are spatial differences in Ca 2+ signalling kinetics. The results showed that each calcium oscillation is built up by 3–4 steps that were generated very quickly and had approximately the same size. Following each Ca 2+ step, there was a slow removal of calcium before the next step boosted the overall level of Ca 2+. Since the Ca 2+ steps were most pronounced directly beneath the plasma membrane, they appear to be generated in this region. The speed of the Ca 2+ wave near the membrane exceeded 40 Lm/s, indicating an active mechanism for wave propagation. In deeper regions of the cell, the wave speed was much slower (about 8 μ/s) and the size of each step was smaller, indicating that regulation occurs within a narrower range of [Ca 2+] i. Inside the nucleus, however, the calcium wave accelerated again (23 μ/s). Treatment with TRH evoked a high amplitude Ca 2+ transient and increased the number of Ca 2+ steps to 5 or 6. Each step had approximately the same size as the steps of the pretreatment Ca 2+ oscillations. Caffeine treatment, which increased the frequency of the oscillations, had no effect on the number or the size of the Ca 2+ steps, but it reduced the time needed for each step to reach its maximum height. We suggest a possible ‘building block’ function for the Ca 2+ steps, whereby a cell generates more steps to achieve a high oscillation amplitude or accelerates the speed of the steps to increase the frequency of oscillations. Both phenomena may play a crucial role in the encoding of information transduced from an extracellular input to the intracellular target.