Figure 2
Figure 2. CD38+/ZAP-70+ CLL cells show enhanced migration in response to SDF-1α. (A) PBMCs from 38 patients with CLL were assayed in the bare-filter chemotaxis assay for migration toward SDF-1α (100 ng/mL). The comparison between CD38+ (n = 15) and CD38− (n = 14) patients (▩) or between ZAP-70+ (n = 15) and ZAP-70− (n = 15) patients (□) is not statistically significant. On the contrary, the results scored by comparing CD38+/ZAP-70+ (n = 11) with CD38−/ZAP-70− (n = 11) or with CD38+/ZAP-70− (n = 8) patients (■) are significantly different. Results are expressed as the mean of the migration indexes, while the error bars indicate the SEM. Statistical difference was calculated according to the Student 2-sample, 2-tailed t test. (B) MFI values for CXCR4 expressed by the 38 patients studied for migration. The comparison between CD38+ (n = 23) and CD38− (n = 16) () is not statistically significant, as opposed to the results scored by comparing ZAP-70+ (n = 17) with ZAP-70− (n = 22) patients (◇) and CD38+/ZAP-70+ (n = 13) with CD38−/ZAP-70− (n = 14) patients (◆). CD38+/ZAP-70− patients (n = 8) featured CXCR4 MFI values not significantly different from CD38−/ZAP-70− patients. (C) Migration was completely abrogated by anti (α)–CXCR4 treatment. Pretreatment with the irrelevant anti (α)–gp120 mAb excluded a nonspecific block. Results are presented as percentage of inhibition of migration in the absence of antibodies and are the means plus or minus SEM of 5 experiments.

CD38+/ZAP-70+ CLL cells show enhanced migration in response to SDF-1α. (A) PBMCs from 38 patients with CLL were assayed in the bare-filter chemotaxis assay for migration toward SDF-1α (100 ng/mL). The comparison between CD38+ (n = 15) and CD38 (n = 14) patients (▩) or between ZAP-70+ (n = 15) and ZAP-70 (n = 15) patients (□) is not statistically significant. On the contrary, the results scored by comparing CD38+/ZAP-70+ (n = 11) with CD38/ZAP-70 (n = 11) or with CD38+/ZAP-70 (n = 8) patients (■) are significantly different. Results are expressed as the mean of the migration indexes, while the error bars indicate the SEM. Statistical difference was calculated according to the Student 2-sample, 2-tailed t test. (B) MFI values for CXCR4 expressed by the 38 patients studied for migration. The comparison between CD38+ (n = 23) and CD38 (n = 16) () is not statistically significant, as opposed to the results scored by comparing ZAP-70+ (n = 17) with ZAP-70 (n = 22) patients (◇) and CD38+/ZAP-70+ (n = 13) with CD38/ZAP-70 (n = 14) patients (◆). CD38+/ZAP-70 patients (n = 8) featured CXCR4 MFI values not significantly different from CD38/ZAP-70 patients. (C) Migration was completely abrogated by anti (α)–CXCR4 treatment. Pretreatment with the irrelevant anti (α)–gp120 mAb excluded a nonspecific block. Results are presented as percentage of inhibition of migration in the absence of antibodies and are the means plus or minus SEM of 5 experiments.

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