USE OF FLUO-3 TO MEASURE CYTOSOLIC CA-2+ IN PLATELETS AND NEUTROPHILS - LOADING CELLS WITH THE DYE, CALIBRATION OF TRACES, MEASUREMENTS IN THE PRESENCE OF PLASMA, AND BUFFERING OF CYTOSOLIC CA-2+

A description is given of the methodology, and problems encountered, for the use of a new fluorescent Ca2+-indicator dye, fluo-3, in neutrophils and platelets. The higher K(d) and longer excitation wavelength of fluo-3 can have significant advantages over fura-2. Although neutrophils and platelets are used as examples, these observations will be applicable to other cell types. The K(d) of fluo-3 for binding Ca2+ at 37°C was measured and found to be 864 nM; the previously published value was 400 nM at 22°C. The K(d) of fluo-3, like that of fura-2, is therefore very temperature-dependent. Protocols for loading cells, and preventing leakage of fluo-3, are described; probenecid, known to inhibit fura-2 leakage from cells, was found to be essential to get good fluo-3 signals from platelets. Calibration of fluo-3 fluorescence signals to [Ca2+] and methods for obtaining maximum and minimum fluorescence signals are described; these methods differ from those used with fura-2. Agonist-stimulated responses of fluo-3-loaded neutrophils and platelets are shown, and the calculated cytosolic [Ca2+] is comparable with that previously obtained with fura-2. Responses of cells in the presence of plasma are also shown; such measurements, unobtainable with quin2, fura-2 or indo-1, are possible with fluo-3, owing to its longer excitation wavelengths. Co-loading of cells with bis-(o-aminophenoxy)ethane-N N N'N'-tetra-acetic acid and fluo-3 is included as an example of how cytosolic [Ca2+] can be buffered and manipulated. Many of these observations will be of value when using fluo-3 (or other Ca2+-indicator dyes) in most cell types.