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IL-2 and Related Cytokines Can Promote T Cell Survival by Activating AKT
Author(s) -
Erin Kelly,
A Jin Won,
Yosef Refaeli,
Luk Van Parijs
Publication year - 2002
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.168.2.597
Subject(s) - protein kinase b , microbiology and biotechnology , signal transduction , cancer research , biology , apoptosis , kinase , immune system , t cell , pi3k/akt/mtor pathway , immunology , biochemistry
The regulated elimination of T cells serves to maintain normal immune function and prevents autoimmune responses. IL-2 family cytokines play an important role in controlling the survival of immature and mature T cells. These molecules activate the protein kinase, AKT/PKB. AKT has been shown to transduce an antiapoptotic signal in numerous cell types. In this study, we show that an active form of AKT can protect T cells from apoptosis following growth factor withdrawal and that IL-2 family cytokines can promote T cell survival by activating this kinase. We also provide evidence that AKT does not block death receptor-mediated killing of lymphocytes. These data suggest that AKT may serve as a common signaling element by which members of the IL-2 family of cytokines promote T cell survival.

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