IL-2 and related cytokines can promote T cell survival by activating AKT

J Immunol. 2002 Jan 15;168(2):597-603. doi: 10.4049/jimmunol.168.2.597.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / pharmacology
  • Apoptosis / immunology
  • B-Lymphocytes / cytology
  • B-Lymphocytes / enzymology
  • B-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / cytology*
  • CD4-Positive T-Lymphocytes / enzymology*
  • CD4-Positive T-Lymphocytes / immunology
  • Cell Survival / immunology
  • Cells, Cultured
  • Cytokines / physiology
  • Enzyme Activation / immunology
  • Interleukin-2 / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • Muramidase / immunology
  • Ovalbumin / immunology
  • Peptide Fragments / immunology
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins / physiology
  • Proto-Oncogene Proteins c-akt
  • Proto-Oncogene Proteins c-bcl-2 / biosynthesis
  • fas Receptor / physiology

Substances

  • Antigens
  • Cytokines
  • Interleukin-2
  • OVA 323-339
  • Peptide Fragments
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor
  • Ovalbumin
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • hen egg lysozyme
  • Muramidase