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Calcium-induced heterogeneous changes in membrane potential detected by flow cytofluorimetry
Authors:John A. Hickman   Owen C. Blair   Anita L. Stepanowski  Alan C. Sartorelli
Affiliation:1. Cancer Research Campaign Experimental Chemotherapy Group, Department of Pharmaceutical Sciences, University of Aston in Birmingham, Birmingham B4 7ET U.K.;2. Department of Pharmacology and Developmental Therapeutics Program, Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT 06510 U.S.A.
Abstract:Ionophore-induced changes in the cell-associated fluorescence of samples of approx. 50 000 individual murine L1210 leukemia cells which had been incubated with the voltage-sensitive dye 3,3′-dihexyloctacarbocyanine iodide (DiOC6(3)) were monitored by flow cytometry. The K+ ionophore valinomycin (1 μM) produced homogeneous changes in the fluorescence of the entire population, the magnitude of which was dependent upon the concentration of extracellular K+. These changes allowed the estimation of the potassium equilibrium potential of the cells, by the null-point method, to be – 11.9 mV. The Ca2+ ionophore A23187 (500 nM) produced heterogeneous changes in fluorescence, with populations of both hyperpolarised and depolarised cells. In addition, the depolarised population underwent an apparent size change, with a reduction in cell volume. This heterogeneity of response resulted in a minimal change in the median fluorescence value for the whole population, which suggests that it would not have been detectable by methods dependent upon net population-averaged changes in fluorescence. Removal of extracellular Na+ or preincubation of cells with amiloride (500 μM) effectively eliminated the depolarised population. Removal of extracellular K+ increased the hyperpolarised population. These findings provide evidence for the presence of Ca2+-induced Na+ exchange and Ca2+-induced K+ efflux mechanisms in these cells which may be expressed simultaneously in the cell population.
Keywords:Membrane potential   Cyanine dye   Na+ -Ca2+ exchange   K+ channel   Fluorescent probe   Flow cytofluorimetry   (Murine leukemia cell)
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