Fig. 4.
Fig. 4. Expression of the HTLV receptor on TCR-stimulated lymphocytes requires de novo protein synthesis. / Freshly isolated CD4+ lymphocytes were activated with immobilized αCD3 and αCD28 mAbs in the absence or presence of the protein synthesis inhibitor cycloheximide (CHX; 5 μg/mL) for 24 hours. The size and density of viable cells were monitored by forward angle light scatter (FSC) and side angle scatter (SSC) on a flow cytometer. HTLV receptor expression as well as CD25 and CD69 levels were assessed using HRBD and the appropriate conjugated mAbs, in the absence and presence of CHX. Filled histograms depict control binding. Data are representative of results obtained in 2 independent experiments.

Expression of the HTLV receptor on TCR-stimulated lymphocytes requires de novo protein synthesis.

Freshly isolated CD4+ lymphocytes were activated with immobilized αCD3 and αCD28 mAbs in the absence or presence of the protein synthesis inhibitor cycloheximide (CHX; 5 μg/mL) for 24 hours. The size and density of viable cells were monitored by forward angle light scatter (FSC) and side angle scatter (SSC) on a flow cytometer. HTLV receptor expression as well as CD25 and CD69 levels were assessed using HRBD and the appropriate conjugated mAbs, in the absence and presence of CHX. Filled histograms depict control binding. Data are representative of results obtained in 2 independent experiments.

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