Simultaneous Analysis of Intracellular pH and Ca2+ from Cell Populations

Although changes in both pHin and [Ca2+ ]i have been observed in response to a variety of agonists, it is not clear whether these ionic events work independently or are coordinated to lead to a specific physiological response. One of the fundamental problems in studying these ionic events is that changes in pHin modify Ca2+ regulatory mechanisms and changes in Ca2+ may modify pH regulation. It is desirable to use a technique that allows concomitant monitoring of these two ions in cell populations with high time resolution. Furthermore, like many Ca2+ binding proteins, all Ca2+ -sensitive fluoroprobes are inherently sensitive to pH owing to competition of H+ for the Ca2+ -binding sites. This chapter describes experimental paradigms that provide optimum conditions for simultaneous measurement of pH from the fluorescence emission of snarf-1, and Ca2+ using fura-2. The fluorescence spectra of these compounds are sufficiently different to allow simultaneous measurement of pH and Ca2+ both in vitro and in vivo. Moreover, the ratio of the H+ -sensitive wavelengths of snarf-1 is unaffected by Ca2+ , or the concomitant presence of fura-2 in cells. Although the fluorescence ratio of fura-2 is insensitive to the presence of snarf-1, it is affected by pH, as indicated above. We describe procedures to correct for this effect and to obtain calibration parameters for fura-2 and snarf-1 required to facilitate analysis of pH and Ca2+ concentrations within cell populations.