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T Helper Cell Differentiation, Heterogeneity, and Plasticity
被引:250
|作者:
Zhu, Jinfang
[1
]
机构:
[1] NIAID, Mol & Cellular Immunoregulat Sect, Lab Immunol, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
来源:
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY
|
2018年
/
10卷
/
10期
基金:
美国国家卫生研究院;
关键词:
INNATE LYMPHOID-CELLS;
TRANSCRIPTION FACTOR GATA-3;
THYMIC STROMAL LYMPHOPOIETIN;
ROR-GAMMA-T;
TGF-BETA;
IN-VIVO;
TH17;
CELLS;
IFN-GAMMA;
TYPE-2;
IMMUNITY;
DENDRITIC CELLS;
D O I:
10.1101/cshperspect.a030338
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Naive CD4T cells, on activation, differentiate into distinct T helper (Th) subsets that produce lineage-specific cytokines. By producing unique sets of cytokines, effector Th subsets play critical roles in orchestrating immune responses to a variety of infections and are involved in the pathogenesis of many inflammatory diseases including autoimmunity, allergy, and asthma. The differentiation of Th cells relies on the strength of T-cell receptor (TCR) signaling and signals triggered by polarizing cytokines that activate and/or up-regulate particular transcription factors. Several lineage-specific master transcription factors dictate Th cell fates and functions. Although these master regulators cross-regulate each other, their expression can be dynamic. Sometimes, they are even coexpressed, resulting in massive Th-cell heterogeneity and plasticity. Similar regulation mediated by these master regulators is also found in innate lymphoid cells (ILCs) that are innate counterparts of Th cells.
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