共 94 条
STAT3 in CD4+ T helper cell differentiation and inflammatory diseases
被引:250
作者:
Egwuagu, Charles E.
[1
]
机构:
[1] NEI, NIH, Immunol Lab, Mol Immunol Sect, Bethesda, MD 20892 USA
来源:
基金:
美国国家卫生研究院;
关键词:
STAT3;
T cell lineage commitment;
CNS inflammatory diseases;
Th17 and Treg development;
Cytokine signaling pathways;
CYTOKINE SIGNALING SOCS;
TRANSCRIPTIONAL REGULATION;
FOXP3;
EXPRESSION;
UNPHOSPHORYLATED STAT3;
ACTIVATION;
GROWTH;
SUPPRESSORS;
APOPTOSIS;
UVEITIS;
INNATE;
D O I:
10.1016/j.cyto.2009.07.003
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
070307 [化学生物学];
071010 [生物化学与分子生物学];
摘要:
Jak/STAT pathways influence cell-fate decisions made by differentiating naive T cells, regulate the intensity and duration of inflammatory responses and are implicated in pathogenic mechanisms of a number of chronic inflammatory diseases. Among the STATs, the STAT3 protein has emerged as an important determinant of whether the naive T cell differentiates into regulatory (Treg) or an inflammatory (Th17) T cell lineage. STAT3 also has potent anti-inflammatory effects and regulates critical cellular processes such as, cell growth, apoptosis and transcription of inflammatory genes. Dysregulation of STAT3 pathway has therefore been implicated in the development of chronic inflammatory diseases, as well as, a number of malignant and neurodegenerative diseases. This review focuses on recent findings regarding the role of STAT3 in immunity, with particular emphasis on T cell lineage specification and disease etiology. New insights from animal models of uveitis, multiple sclerosis and inflammatory bowel diseases are discussed as exemplars of critical roles that STAT3 pathways play in inflammatory diseases and on how inhibiting STAT3 can be exploited to mitigate pathogenic autoimmunity. Published by Elsevier Ltd.
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页码:149 / 156
页数:8
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