Objective As the photostability of calcium ions (Ca2+) indicators is an important property for indicating the temporal features of cytosolic Ca2+ in cells, this study aims to quantitatively measure the light-induced fluorescence enhancement in cells stained with Ca2+ indicators. Methods Five cell lines, MC3T3-E1, RAW264.7, MLO-Y4, MEF3T3 and HEK293, were exposed to the light with five levels of optical power, respectively, so as to investigate the light induced responses of two commonly-used Ca2+ indicators, Fluo-4 AM and Oregon green. The light-induced fluorescence enhancement, the succeeding photobleaching and the thapsigargin (TG)-induced responsive peak followed by were observed. The characteristic parameters of responsive peaks were further analyzed. Results Light with higher power level would induce the fluorescence enhancement for both Fluo-4 AM or Oregon green, while the responsive percentage as well as the magnitude and time span of light-induced peak of Oregon green-stained cells were significantly lower than those of Fluo-4 AM-stained cells. Conclusions The use of Oregon green with low power level light shows better photostability to indicate the intracellular Ca2+.