Ligand-induced autoregulation of IL-2 receptor {alpha} chain expression in murine T cell lines |
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Authors: | Demaison, Christophe Chastagner, Patricia Moreau, Jean-Louis Theze, Jacques |
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Affiliation: | Unité d'immunogénétique Cellulaire, Institut Pasteur 25 rue du D. Roux, 75015 Paris, France |
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Abstract: | The IL-2 receptor (IL-2R) is composed of three chains a, ßand . In mice, contrary to the human system, we have previouslydemonstrated that the IL-2Rß complex does not bindIL-2. Therefore, mouse IL-2 response is completely dependenton the expression of the IL-2R gene product. T cell clones expressingmouse IL-2Rß and the human IL-2R transgene have beenstudied. When cells are grown in IL-4, mouse IL-2R is not expressed.However, exposure to IL-2 leads to the expression of the endogenousmurine IL-2R subunit. The T cell line expressing mouse IL-2Rand human IL-2Rß can grow in IL-2 but does not expressendogenous murine IL-2 R. Transfection of these cells with thehuman IL-2R gene restores the capacity to induce murine IL-2R.This result demonstrates that IL-2-IL-2R interactions are requiredfor induction of IL-2R. The kinetics of induction and deinductionof murine IL-2R have been studied using clone 18.III. From negativecells, expression of murine IL-2R is a very slow phenomenon.From cells fully expressing IL-2R, deinduction is a two-stepprocess: after a rapid decrease of IL-2R the cells continueto express, for a long period of time, basal levels of murineIL-2R. When cells expressing basal levels of IL-2R are exposedto IL-2, induction of IL-2R is a very rapid phenomenon. Theautoregulatory loop formed by IL-2-IL-2R therefore displaysdifferent levels of functioning. |
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Keywords: | activation, cytokine responsiveness, IL-2, IL-2 receptor /math/alpha.gif" ALT=" {alpha}" BORDER=" 0" >, ß and /math/gamma.gif" ALT=" {gamma}" BORDER=" 0" > chains, proliferation, T cell |
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