Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1933806 | Biochemical and Biophysical Research Communications | 2009 | 5 Pages |
Abstract
Interleukin-2 (IL-2) is a cytokine that regulates proliferation, differentiation and survival of various lymphoid cell subsets. Its actions are mediated through its binding to the IL-2 receptor which is composed of three subunits (IL-2Rα, IL-2Rβ and γc). Only β and γc have been shown to transduce intra cellular signals. The γc chain is shared by the interleukin-2, 4, 7, 9, 15 and 21 receptors, and is essential for lymphocyte functions. The regulation of γc expression level is therefore critical for the ability of cells to respond to these cytokines. In the present work, we show that the IL-2R constitutively associates with the ubiquitin ligase NEDD4-2, and to a lesser extent NEDD4-1. We identified the specific binding site on γc. And we show that the loss of NEDD4 association on γc is accompanied by a dramatic increase of the half-life of the receptor subunit.
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Authors
Valérie Malardé, Richard Proust, Alice Dautry-Varsat, Franck Gesbert,