Mouse CD4+ CD25+ T regulatory cells are protected from autologous complement mediated injury by Crry and CD59

被引:6
|
作者
Li, Qing [1 ,2 ]
Nacion, Kristine [2 ]
Bu, Hong [1 ]
Lin, Feng [1 ,2 ]
机构
[1] Sichuan Univ, Dept Pathol, Chengdu 610064, Peoples R China
[2] Case Western Reserve Univ, Inst Pathol, Cleveland, OH 44106 USA
关键词
Complement; Complement regulators; Treg cells; Foxp3; Mouse; DECAY-ACCELERATING FACTOR; MEMBRANE COFACTOR PROTEIN; HOMOLOGOUS RESTRICTION FACTOR; GLOMERULAR EPITHELIAL-CELLS; NATURAL-KILLER-CELLS; FACTOR DAF; RECEPTOR CR-1; ACTIVATION; EXPRESSION; SURFACE;
D O I
10.1016/j.bbrc.2009.03.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self cells depend on surface complement regulators to protect them from autologous complement-mediated attack. CD4(+)CD25(+)foxp3(+) T regulatory (Treg) cells are critical in maintaining immune homeostasis, however, which complement regulators are expressed on them and how they are protected from autologous complement attack remains unknown. We report here that mouse Treg cells express virtually no DAF or CRI. Instead, all of them express Crry and approximately half of them express CD59. Both Crry(-/-) and CD59(-/-) Treg cells exhibit greater complement mediated injury than WT Treg cells. These results clarify the status of cell surface complement regulators on mouse Treg cells and indicate that both Crry and CD59 are required to protect Treg cells from autologous complement-mediated injury. Additionally, these data also argue that different from previous assumption, at least in mice, CD4(+)CD25(+)foxp3(+) Treg cells are not homogenous and could be further divided into subgroups based on CD59 expression. (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:223 / 226
页数:4
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