Transcriptional regulation of T lymphocyte development and function

CT Kuo, JM Leiden - Annual review of immunology, 1999 - annualreviews.org
CT Kuo, JM Leiden
Annual review of immunology, 1999annualreviews.org
▪ 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 …
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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