Innate and adaptive immune responses regulated by glycogen synthase kinase-3 (GSK3)

被引:314
作者
Beurel, Eleonore [1 ]
Michalek, Suzanne M. [2 ]
Jope, Richard S. [1 ]
机构
[1] Univ Alabama, Dept Psychiat, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
T-CELL-ACTIVATION; BETA-CATENIN; INTERFERON-GAMMA; KAPPA-B; GLYCOGEN-SYNTHASE-KINASE-3-BETA INHIBITION; CEREBRAL ISCHEMIA/REPERFUSION; CYTOKINE PRODUCTION; CD28; COSTIMULATION; SIGNALING PATHWAY; MOOD STABILIZERS;
D O I
10.1016/j.it.2009.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In just a few years, the view of glycogen synthase kinase-3 (GSK3) has been transformed from an obscure enzyme seldom encountered in the immune literature to one implicated in an improbably large number of roles. GSK3 is a crucial regulator of the balance between pro- and anti-inflammatory cytokine production in both the periphery and the central nervous system, so that GSK3 inhibitors such as lithium can diminish inflammation. GSK3 influences T-cell proliferation, differentiation and survival. Many effects stem from GSK3 regulation of critical transcription factors, such as NF-kappa B, NFAT and STATs. These discoveries led to the rapid application of GSK3 inhibitors to animal models of sepsis, arthritis, colitis, multiple sclerosis and others, demonstrating their potential for therapeutic intervention.
引用
收藏
页码:24 / 31
页数:8
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