RETRACTED: Uncoupling IL-2 signals that regulate T cell proliferation, survival, and Fas-mediated activation-induced cell death (Retracted article. See vol. 30, pg. 611, 2009)

被引:368
作者
Van Parijs, L
Refaeli, Y
Lord, JD
Nelson, BH
Abbas, AK
Baltimore, D [1 ]
机构
[1] CALTECH, Dept Biol, Pasadena, CA 91125 USA
[2] Brigham & Womens Hosp, Div Immunol Res, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Univ Washington, Virginia Mason Res Ctr, Seattle, WA 98195 USA
[5] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
关键词
D O I
10.1016/S1074-7613(00)80103-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-2 is an important growth and survival factor for T lymphocytes but also sensitizes these cells to Fas-mediated activation-induced cell death (AICD). The molecular basis of these different effects of IL-2 was studied by introducing wild-type and mutant forms of the IL-2 receptor beta (IL-2R beta) chain that lacked specific signaling capacities into receptor-deficient T cells by retroviral gene transfer. Activation of Stat5 by IL-2 was found to be involved in T cell proliferation and promoted Pas ligand (FasL) expression and AICD. T cell survival was dependent on a receptor region that activated Akt and the expression of Bcl-2. Thus, distinct IL-2R beta chain signaling modules regulate T cell fate by stimulating growth and survival or by promoting apoptosis.
引用
收藏
页码:281 / 288
页数:8
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