Water-soluble protein signals (pheromones) of the ciliate Euplotes have been supposed to be functional precursors of growth factors and cytokines that regulate cell–cell interactionin multi-cellular eukaryotes.This work provides evidence that native preparations of the Euplotes raikovi pheromone Er-1 (a helical protein of 40 aminoacids) specifically increases viability, DNA synthesis, proliferation, and the production of interferon-g, tumor necrosis factor-a, interleukin (IL)-1b, IL-2, and IL-13 in human Jurkat T-cells. Also, Er-1 significantly decreases them RNA levels of the b and g subunits of IL-2 receptor(IL-2R), while them RNA levels of the a subunit appeared to be not affected. Jurkat T-cell treatments with Er-1 induced the down-regulation of the IL-2Ra subunit by a reversible and time-dependent endocytosis, and increased the levels of phosphorylation of the extracellular signal-regulated kinases (ERK). The cell-type specificity of these effects was supported by the finding that Er-1, although unable to directly influence the growth of human glioma U373 cells, induced Jurkat cells to synthesize and release factors that, in turn, inhibited the U373 cell proliferation. Overall, these findings imply that Er-1 coupling to IL-2R and ERK immuno-enhances T-cell activity, and that this effect likely translates to an inhibition of glioma cell growth.

The protein pheromone Er-1 of the ciliate Euplotes raikovi stimulates humanT-cell activity: Involvement of interleukin-2 system

ALIMENTI, Claudio;VALLESI, Adriana
2013-01-01

Abstract

Water-soluble protein signals (pheromones) of the ciliate Euplotes have been supposed to be functional precursors of growth factors and cytokines that regulate cell–cell interactionin multi-cellular eukaryotes.This work provides evidence that native preparations of the Euplotes raikovi pheromone Er-1 (a helical protein of 40 aminoacids) specifically increases viability, DNA synthesis, proliferation, and the production of interferon-g, tumor necrosis factor-a, interleukin (IL)-1b, IL-2, and IL-13 in human Jurkat T-cells. Also, Er-1 significantly decreases them RNA levels of the b and g subunits of IL-2 receptor(IL-2R), while them RNA levels of the a subunit appeared to be not affected. Jurkat T-cell treatments with Er-1 induced the down-regulation of the IL-2Ra subunit by a reversible and time-dependent endocytosis, and increased the levels of phosphorylation of the extracellular signal-regulated kinases (ERK). The cell-type specificity of these effects was supported by the finding that Er-1, although unable to directly influence the growth of human glioma U373 cells, induced Jurkat cells to synthesize and release factors that, in turn, inhibited the U373 cell proliferation. Overall, these findings imply that Er-1 coupling to IL-2R and ERK immuno-enhances T-cell activity, and that this effect likely translates to an inhibition of glioma cell growth.
2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11581/250272
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