Figure 6
Effect of Aiolos on apoptosis in B cells from CLL patients. (A) Influence of Aiolos knockdown and Aiolos overexpression on antiapoptotic gene expression analyzed by qRT-PCR and normalized by use of the 2−ΔCt calculation method (Ct indicates cycle threshold) and β-actin as reference gene. Results are expressed as fold down- or up-regulation of transfected cells by pcDNA3.1-Flag-Aio-1 vector or Aiolos siRNA compared with transfected cells by pcDNA3.1-Flag vector or nontargeting negative control siRNA, respectively. The histograms represent the mean ± SD of genes down-regulation (n = 3, left) or up-regulation (n = 2, right). (B) PMA/ionomycin-induced cell death assayed by AV/PI double staining and flow cytometry. B cells from CLL patients transfected with pcDNA-Flag-Aio-1 or pcDNA-Flag vector. Eighteen hours after transfection, cells were stimulated by PMA and ionomycin (10 ng/mL and 1 μg/mL) for 8 hours before apoptosis analysis. Representative dot plots show AV/PI staining on B cells from patient P44. Percentages of viable (AV−/PI−), apoptotic (AV+/PI−), secondary apoptotic/necrotic (AV+/PI+), and necrotic (AV−/PI+) populations are indicated (left). The histograms represent the mean proportions of AV−/PI−, AV+/PI−, AV+/PI+, and AV−/PI+ cells obtained with cells from 5 patients (P37-39, P43, P44; right).

Effect of Aiolos on apoptosis in B cells from CLL patients. (A) Influence of Aiolos knockdown and Aiolos overexpression on antiapoptotic gene expression analyzed by qRT-PCR and normalized by use of the 2−ΔCt calculation method (Ct indicates cycle threshold) and β-actin as reference gene. Results are expressed as fold down- or up-regulation of transfected cells by pcDNA3.1-Flag-Aio-1 vector or Aiolos siRNA compared with transfected cells by pcDNA3.1-Flag vector or nontargeting negative control siRNA, respectively. The histograms represent the mean ± SD of genes down-regulation (n = 3, left) or up-regulation (n = 2, right). (B) PMA/ionomycin-induced cell death assayed by AV/PI double staining and flow cytometry. B cells from CLL patients transfected with pcDNA-Flag-Aio-1 or pcDNA-Flag vector. Eighteen hours after transfection, cells were stimulated by PMA and ionomycin (10 ng/mL and 1 μg/mL) for 8 hours before apoptosis analysis. Representative dot plots show AV/PI staining on B cells from patient P44. Percentages of viable (AV/PI), apoptotic (AV+/PI), secondary apoptotic/necrotic (AV+/PI+), and necrotic (AV/PI+) populations are indicated (left). The histograms represent the mean proportions of AV/PI, AV+/PI, AV+/PI+, and AV/PI+ cells obtained with cells from 5 patients (P37-39, P43, P44; right).

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