Figure 3.
Figure 3. CD38 expression is associated with elevated basal Ca2+ levels. MEC1-GFP, MEC1-CD38H, and primary CLL cells with varying CD38 expression levels (n = 17 patient samples, analyzed in 3 independent experiments) were incubated with the ratiometric Ca2+ indicator Indo-1 and analyzed by flow cytometry. The basal fluorescence level was recorded for 60 seconds before stimulation with CCL21 (100 ng/mL) for a further 120 seconds. (A,C) Representative bivariate plot of the median of fluorescent intensity ratio (Indo-1 emission wavelengths: 420/510 nm) against time; red boxes indicate the basal fluorescence level. (B,D) Peak values of the median basal fluorescence intensity were obtained using FlowJo Kinetic statistic tool. Horizontal bars in panel D indicate mean values of the fluorescence intensity peak calculated in each experiment for CD38low (green) and CD38high (red) samples. Significant differences between the 2 experimental groups were determined using a 2-tailed Student t test.

CD38 expression is associated with elevated basal Ca2+levels. MEC1-GFP, MEC1-CD38H, and primary CLL cells with varying CD38 expression levels (n = 17 patient samples, analyzed in 3 independent experiments) were incubated with the ratiometric Ca2+ indicator Indo-1 and analyzed by flow cytometry. The basal fluorescence level was recorded for 60 seconds before stimulation with CCL21 (100 ng/mL) for a further 120 seconds. (A,C) Representative bivariate plot of the median of fluorescent intensity ratio (Indo-1 emission wavelengths: 420/510 nm) against time; red boxes indicate the basal fluorescence level. (B,D) Peak values of the median basal fluorescence intensity were obtained using FlowJo Kinetic statistic tool. Horizontal bars in panel D indicate mean values of the fluorescence intensity peak calculated in each experiment for CD38low (green) and CD38high (red) samples. Significant differences between the 2 experimental groups were determined using a 2-tailed Student t test.

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