Figure 2.
Figure 2. Method used to investigate the PMCA Vmax distribution in RBCs. (Panel A) Computer simulation of the Ca2+ load-extrusion protocol in an RBC population whose symmetrical distribution of PMCA Vmax activity is shown in the inset. Substrate-fed RBCs are assumed to be suspended at an Hct of approximately 10% in an iso-osmotic buffer containing 80 mM K+ and 100 μM CaCl2 at 37°C with magnetic stirring. A high ionophore concentration is used to rapidly induce a large and uniform RBC Ca2+ load. After about 2 minutes (to prevent significant reduction of cell ATP levels) Co2+ is added in excess of Ca2+ in the medium to block ionophore-mediated Ca2+ transport and to expose the uphill extrusion of Ca2+ by the pump. [CaT]i was estimated in timed samples with the use of 45Ca by dividing the measured cell-contained 45Ca radioactivity by the specific activity of 45Ca (there are no endogenous Ca2+ pools that could dilute the specific activity set by the addition of tracer). Each of the Ca2+ extrusion curves was obtained by solving numerically the differential equation d[Ca2+]i /dt = (Vmax)([Ca2+]i2/(Kd2 + [Ca2+]i2)), using a different Vmax value for each curve and applying the conversion [CaT]i = [Ca2+]i /α (Figure 1 legend). The thick line was computed as the weighted mean of the Vmax distribution shown in the inset. Note that the Ca2+-extrusion curves with different Vmax remain linear until [CaT]i falls to about 2 to 4 μM, as expected from a Ca2+ desaturation kinetics with Kd values in the range of 0.2 to 0.5 μM.2,4,36 The mean-Vmax curve also renders a linear segment with a slope close to the true mean Vmax of the distribution (approximately 14 mmol (340 g Hb)-1h-1) but with an apparent Ca2+ desaturation pattern starting at [CaT]i approximately 100 μmol (340 g Hb)-1 a level much higher than that of the single-Vmax desaturation curves. This specious desaturation effect results from retention of Ca2+ within the low-Vmax cells. Points A to E mark sampling times for hemolysis curves expected to have the patterns illustrated in panel B. The horizontal dashed line is at the [CaT]i level above which Gardos channels are assumed to open maximally. (Panel B) Actual hemolysis curves from preliminary experiments illustrate the patterns expected with samples taken at the time points A (▴) to E (•) of the load-extrusion protocol simulated in panel A.

Method used to investigate the PMCA Vmaxdistribution in RBCs. (Panel A) Computer simulation of the Ca2+ load-extrusion protocol in an RBC population whose symmetrical distribution of PMCA Vmax activity is shown in the inset. Substrate-fed RBCs are assumed to be suspended at an Hct of approximately 10% in an iso-osmotic buffer containing 80 mM K+ and 100 μM CaCl2 at 37°C with magnetic stirring. A high ionophore concentration is used to rapidly induce a large and uniform RBC Ca2+ load. After about 2 minutes (to prevent significant reduction of cell ATP levels) Co2+ is added in excess of Ca2+ in the medium to block ionophore-mediated Ca2+ transport and to expose the uphill extrusion of Ca2+ by the pump. [CaT]i was estimated in timed samples with the use of 45Ca by dividing the measured cell-contained 45Ca radioactivity by the specific activity of 45Ca (there are no endogenous Ca2+ pools that could dilute the specific activity set by the addition of tracer). Each of the Ca2+ extrusion curves was obtained by solving numerically the differential equation d[Ca2+]i /dt = (Vmax)([Ca2+]i2/(Kd2 + [Ca2+]i2)), using a different Vmax value for each curve and applying the conversion [CaT]i = [Ca2+]i /α (Figure 1 legend). The thick line was computed as the weighted mean of the Vmax distribution shown in the inset. Note that the Ca2+-extrusion curves with different Vmax remain linear until [CaT]i falls to about 2 to 4 μM, as expected from a Ca2+ desaturation kinetics with Kd values in the range of 0.2 to 0.5 μM.2,4,36  The mean-Vmax curve also renders a linear segment with a slope close to the true mean Vmax of the distribution (approximately 14 mmol (340 g Hb)-1h-1) but with an apparent Ca2+ desaturation pattern starting at [CaT]i approximately 100 μmol (340 g Hb)-1 a level much higher than that of the single-Vmax desaturation curves. This specious desaturation effect results from retention of Ca2+ within the low-Vmax cells. Points A to E mark sampling times for hemolysis curves expected to have the patterns illustrated in panel B. The horizontal dashed line is at the [CaT]i level above which Gardos channels are assumed to open maximally. (Panel B) Actual hemolysis curves from preliminary experiments illustrate the patterns expected with samples taken at the time points A (▴) to E (•) of the load-extrusion protocol simulated in panel A.

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