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

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

  • Blood. 2007 Sep 1;110(5):1550-8. doi: 10.1182/blood-2007-01-069229.
Jan Kubach 1 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
Affiliations

Affiliation

  • 1 Department of Dermatology, Johannes Gutenberg-University, Mainz, Germany.
Abstract

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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