MIP-1alpha, MIP-1beta, RANTES, and ATAC/lymphotactin function together with IFN-gamma as type 1 cytokines

Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6181-6. doi: 10.1073/pnas.092141999. Epub 2002 Apr 23.

Abstract

We analyzed for the first time the expression of chemokines in subpopulations of the murine immune system at the single-cell level. We demonstrate in vitro and in a model of murine listeriosis that macrophage inflammatory protein (MIP)-1alpha, MIP-1beta, regulated on activation normal T cell expressed and secreted (RANTES), and activation-induced, T cell-derived, and chemokine-related cytokine (ATAC)/lymphotactin are cosecreted to a high degree with IFN-gamma by activated individual natural killer (NK), CD8(+) T, and CD4(+) T helper 1 (Th1) cells. Functionally, ATAC and the CC chemokines cooperate with IFN-gamma in the up-regulation of CD40, IL-12, and tumor necrosis factor-alpha, molecules playing a central role in the effector phase of macrophages. Our data indicate that (i) MIP-1alpha, MIP-1beta, RANTES, and ATAC are not only chemoattractants but also coactivators of macrophages, (ii) MIP-1alpha, MIP-1beta, RANTES, and ATAC constitute together with IFN-gamma a group of "type 1 cytokines," and (iii) these cytokines act together as a functional unit that is used by NK cells in the innate phase and then "handed over" to CD8(+) T cells in the antigen-specific phase of the immune defense, thus bridging the two components of a Th1 immune reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Marrow Cells / metabolism
  • CD8-Positive T-Lymphocytes / metabolism*
  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5 / metabolism*
  • Chemokines, C*
  • Flow Cytometry
  • Interferon-gamma / metabolism*
  • Interleukin-12 / biosynthesis
  • Killer Cells, Natural / metabolism
  • Listeria monocytogenes / metabolism
  • Lymphokines / metabolism*
  • Macrophage Inflammatory Proteins / metabolism*
  • Macrophages / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Models, Biological
  • Protein Binding
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sialoglycoproteins / metabolism*
  • Spleen / cytology
  • Spleen / microbiology
  • Th1 Cells / cytology
  • Th2 Cells / cytology
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Up-Regulation

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Chemokine CCL5
  • Chemokines, C
  • Lymphokines
  • Macrophage Inflammatory Proteins
  • Sialoglycoproteins
  • Tumor Necrosis Factor-alpha
  • Xcl1 protein, mouse
  • lymphotactin
  • Interleukin-12
  • Interferon-gamma