Fig. 5.
Fig. 5. Induction of HTLV receptor expression on IL-7–stimulated neonatal CD4+ lymphocytes. / (A) Adult and neonatal CD4+ T cells were isolated from adult peripheral blood (APB) and umbilical cord blood (UC), respectively, and cultured for 7 days in the presence of recombinant IL-7 (10 ng/mL). Expression of the HTLV and amphotropic MLV receptors as well as CD25 levels were monitored by FACS using HRBD, ARBD, and a PE-conjugated αCD25 mAb. Filled histograms depict control binding. (B) Cell cycle entry of IL-7–stimulated APB and UC CD4+ lymphocytes was monitored at day 7 by assessing the DNA content of PI-stained cells on FACS. Results are representative of data obtained in 3 independent experiments.

Induction of HTLV receptor expression on IL-7–stimulated neonatal CD4+ lymphocytes.

(A) Adult and neonatal CD4+ T cells were isolated from adult peripheral blood (APB) and umbilical cord blood (UC), respectively, and cultured for 7 days in the presence of recombinant IL-7 (10 ng/mL). Expression of the HTLV and amphotropic MLV receptors as well as CD25 levels were monitored by FACS using HRBD, ARBD, and a PE-conjugated αCD25 mAb. Filled histograms depict control binding. (B) Cell cycle entry of IL-7–stimulated APB and UC CD4+ lymphocytes was monitored at day 7 by assessing the DNA content of PI-stained cells on FACS. Results are representative of data obtained in 3 independent experiments.

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