Store depletion induces Ca2+ entry in hTrp3-transfected
wild-type DT40 cells. Fura-2-loaded wild-type DT40 cells transfected
with either hTrp3 or its vector (Mock), along with a construct encoding
eGFP as transfection marker (see Materials and Methods),
were incubated in a nominally Ca2+-free medium and then
exposed to 2 μM thapsigargin to deplete intracellular
Ca2+ stores. After cytosolic Ca2+ returned to
basal levels, Ca2+ (1.5 mM) was re-added to the medium.
Shown are average curves ± SEM (in gray) from three independent
experiments, each of them performed on at least four single cells.
Measurements were performed on positively transfected cells, which were
selected by their green fluorescence when excited at 488 nm
(eGFP-positive cells).