Murine T helper type 2 clones were stimulated with immobilized anti-CD3 antibody or with recombinant lymphokines to compare the expression of T-cell activation genes induced by these stimuli. Immobilized anti-CD3 antibody, recombinant interleukin 2 (IL-2), and recombinant Interleukin 4 (IL-4) all induced proliferation of the T helper type 2 clones 10-5-17 and D10. Proliferation of these clones Induced by anti-CD3 antibody was completely inhibited by cyclosporine A, whereas cyclosporine A had little effect on proliferation induced by recombinant IL-2 or recombinant IL-4. Both immobilized anti-CD3 antibody, and recombinant IL-2 induced the expression of the protooncogenes c-myc and c-myb. Immobilized anti-CD3 antibody also induced expression of the lymphokine genes IL-4, interleukin 5 (IL-5), and granulocyte-macrophage colony-stimulating factor. In contrast, recombinant IL-2 induced IL-5 mRNA expression but did not induce detectable expression of IL-4 or granulocyte-macrophage colony-stimulating factor mRNA. Likewise, recombi-nant IL-4 induced expression of IL-5 but not IL-4 mRNA. Thus, the IL-4 and IL-5 genes appear to be differentially regulated after stimulation with recombinant lymphokines. Effects of cyclosporine A and the protein synthesis inhibitors cycloheximide and anisomycin on IL-4 and IL-5 gene expres-sion suggest that these genes are activated by different pathways after anti-CD3 stimulation. Cyclosporine A completely Inhibited anti-CD3-induced expression of IL-4 mRNA but not of IL-5 mRNA, and protein-synthesis inhibitors completely Inhibited induction of IL-5 mRNA but not of IL-4 mRNA. Together, our data show that T-cell receptor-mediated and cytophokine receptor-mediated signals induce different pat-of lymphokine gene expression and provide strong evi-dance that the IL-4 and IL-5 genes are differentially regulated. (.
CITATION STYLE
Bohjanen, P. R., Okajima, M., & Hodes, R. J. (1990). Differential regulation of interleukin 4 and interleukin 5 gene expression: A comparison of T-cell gene induction by anti-CD3 antibody or by exogenous lymphokines. Proceedings of the National Academy of Sciences of the United States of America, 87(14), 5283–5287. https://doi.org/10.1073/pnas.87.14.5283
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