Fig. 2: cAMP signal propagation in a chemotactic giant cell.

a Time-lapse fluorescence images of Flamindo2-expressing giant cells after starvation for 7 h in DB showing spatial changes in cytoplasmic cAMP levels (inverted intensity). Fluorescence imaging was performed using a confocal microscope with a 40× objective. Cells were observed at 5 s intervals. The elapsed time from the start of imaging was shown. Scale bars: 20 μm. b Kymograph of cAMP signal intensity extracted from the white rectangle in (a) (46 µm in length), showing an earlier increase at the front (F) and an earlier decrease at the rear (R) over time.