Human CD4+CD25+ regulatory T cells: proteome analysis identifies galectin-10 as a novel marker essential for their anergy and suppressive function.

نویسندگان

  • Jan Kubach
  • Petra Lutter
  • Tobias Bopp
  • Sabine Stoll
  • Christian Becker
  • Eva Huter
  • Christoph Richter
  • Petra Weingarten
  • Tobias Warger
  • Jürgen Knop
  • Stefan Müllner
  • John Wijdenes
  • Hansjörg Schild
  • Edgar Schmitt
  • Helmut Jonuleit
چکیده

CD4(+)CD25(+)Foxp3(+) regulatory T cells (CD25(+) Treg cells) direct the maintenance of immunological self-tolerance by active suppression of autoaggressive T-cell populations. However, the molecules mediating the anergic state and regulatory function of CD25(+) Treg cells are still elusive. Using differential proteomics, we identified galectin-10, a member of the lectin family, as constitutively expressed in human CD25(+) Treg cells, while they are nearly absent in resting and activated CD4(+) T cells. These data were confirmed on the mRNA and protein levels. Single-cell staining and flow cytometry showed a strictly intracellular expression of galectin-10 in CD25(+) Treg cells. Specific inhibition of galectin-10 restored the proliferative capacity of CD25(+) Treg cells and abrogated their suppressive function. Notably, first identified here as expressed in human T lymphocytes, galectin-10 is essential for the functional properties of CD25(+) Treg cells.

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عنوان ژورنال:
  • Blood

دوره 110 5  شماره 

صفحات  -

تاریخ انتشار 2007