生物
NFAT公司
转录因子
细胞生物学
信号转导
关贸总协定3
Mef2
T细胞
奶油
抄写(语言学)
转录调控
增强子
基因
遗传学
免疫系统
语言学
哲学
作者
Chay T. Kuo,Jeffrey M. Leiden
出处
期刊:Annual Review of Immunology
[Annual Reviews]
日期:1999-04-01
卷期号:17 (1): 149-187
被引量:293
标识
DOI:10.1146/annurev.immunol.17.1.149
摘要
▪ Abstract The development and function of T lymphocytes are regulated tightly by signal transduction pathways that include specific cell-surface receptors, intracellular signaling molecules, and nuclear transcription factors. Since 1988, several families of functionally important T cell transcription factors have been identified. These include the Ikaros, LKLF, and GATA3 zinc-finger proteins; the Ets, CREB/ATF, and NF-κB/Rel/NFAT transcription factors; the Stat proteins; and HMG box transcription factors such as LEF1, TCF1, and Sox4. In this review, we summarize our current understanding of the transcriptional regulation of T cell development and function with particular emphasis on the results of recent gene targeting and transgenic experiments. In addition to increasing our understanding of the molecular pathways that regulate T cell development and function, these results have suggested novel targets for genetic and pharmacological manipulation of T cell immunity.
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