Fig. 5.
Fig. 5. Heterodimerization of the cytoplasmic domain of βIL3 and IL3 induces mitogenesis in CTLL-2 cells. (A) Flow cytometric analysis confirming expression of the hCD8 chimeric receptors. Thin lines represent results with cells treated with FITC-coupled secondary antibody alone; thick lines represent results with cells treated with CD8 and FITC-coupled secondary antibody. (B) Immunoprecipitation of surface biotinylated proteins confirming expression of both CD8/ and CD8/β in doubly transfected cells as described in the legend to Fig 4B. Lane 1, parental CTLL-2; lane 2, CTLL-2 transfected with CD8/βIL-3; lane 3, CTLL-2 transfected with CD8/IL-3; lane 4, CTLL-2 transfected with CD8/IL-3 and CD8/βIL-3. (C) [3H]-thymidine incorporation of transfectants in the absence of IL-2. Cells were cultured with or without IL-2 for 40 hours and then incubated for an additional 8 hours in the presence of [3H]-thymidine. Data are plotted as the percent of maximal incorporation observed in IL-2. Error bars represent the SEM of triplicate samples.

Heterodimerization of the cytoplasmic domain of βIL3 and IL3 induces mitogenesis in CTLL-2 cells. (A) Flow cytometric analysis confirming expression of the hCD8 chimeric receptors. Thin lines represent results with cells treated with FITC-coupled secondary antibody alone; thick lines represent results with cells treated with CD8 and FITC-coupled secondary antibody. (B) Immunoprecipitation of surface biotinylated proteins confirming expression of both CD8/ and CD8/β in doubly transfected cells as described in the legend to Fig 4B. Lane 1, parental CTLL-2; lane 2, CTLL-2 transfected with CD8/βIL-3; lane 3, CTLL-2 transfected with CD8/IL-3; lane 4, CTLL-2 transfected with CD8/IL-3 and CD8/βIL-3. (C) [3H]-thymidine incorporation of transfectants in the absence of IL-2. Cells were cultured with or without IL-2 for 40 hours and then incubated for an additional 8 hours in the presence of [3H]-thymidine. Data are plotted as the percent of maximal incorporation observed in IL-2. Error bars represent the SEM of triplicate samples.

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