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

被引:170
作者
Kubach, Jan
Lutter, Petra
Bopp, Tobias
Stoll, Sabine
Becker, Christian
Huter, Eva
Richter, Christoph
Weingarten, Petra
Warger, Tobias
Knop, Juergen
Muellner, Stefan
Wijdenes, John
Schild, Hansjrg
Schmitt, Edgar
Jonuleit, Helmut
机构
[1] Univ Mainz, Dept Dermatol, D-55101 Mainz, Germany
[2] Protagen AG, Dortmund, Germany
[3] Univ Mainz, Inst Immunol, D-6500 Mainz, Germany
[4] Diaclone SAS, Besancon, France
关键词
D O I
10.1182/blood-2007-01-069229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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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收藏
页码:1550 / 1558
页数:9
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