共 48 条
Helios Expression Is a Marker of T Cell Activation and Proliferation
被引:298
作者:

Akimova, Tatiana
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA
Univ Penn, Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA

Beier, Ulf H.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Penn, Sch Med, Philadelphia, PA 19104 USA
Childrens Hosp Philadelphia, Dept Pediat, Div Nephrol, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA

Wang, Liqing
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA
Univ Penn, Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA

Levine, Matthew H.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Penn, Sch Med, Philadelphia, PA 19104 USA
Hosp Univ Penn, Penn Transplant Inst, Dept Surg, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA

Hancock, Wayne W.
论文数: 0 引用数: 0
h-index: 0
机构:
Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA
Univ Penn, Sch Med, Philadelphia, PA 19104 USA Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA
机构:
[1] Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Div Transplant Immunol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Dept Pediat, Div Nephrol, Philadelphia, PA 19104 USA
[4] Hosp Univ Penn, Penn Transplant Inst, Dept Surg, Philadelphia, PA 19104 USA
来源:
PLOS ONE
|
2011年
/
6卷
/
08期
基金:
美国国家卫生研究院;
关键词:
TRANSCRIPTION FACTOR;
SUPPRESSIVE FUNCTION;
FOXP3;
LOCUS;
IKAROS;
TNFR2;
DIFFERENTIATION;
SPECIFICATION;
GENERATION;
INHIBITION;
PROMOTES;
D O I:
10.1371/journal.pone.0024226
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Foxp3+ T-regulatory cells (Tregs) normally serve to attenuate immune responses and are key to maintenance of immune homeostasis. Over the past decade, Treg cells have become a major focus of research for many groups, and various functional subsets have been characterized. Recently, the Ikaros family member, Helios, was reported as a marker to discriminate naturally occurring, thymic-derived Tregs from those peripherally induced from naive CD4+ T cells. We investigated Helios expression in murine and human T cells under resting or activating conditions, using well-characterized molecules of naive/effector/memory phenotypes, as well as a set of Treg-associated markers. We found that Helios-negative T cells are enriched for naive T cell phenotypes and vice versa. Moreover, Helios can be induced during T cell activation and proliferation, but regresses in the same cells under resting conditions. We demonstrated comparable findings using human and murine CD4+ Foxp3+ Tregs, as well as in CD4+ and CD8+ T cells. Since Helios expression is associated with T cell activation and cellular division, regardless of the cell subset involved, it does not appear suitable as a marker to distinguish natural and induced Treg cells.
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