Activating transcription factor 3 and the nervous system

被引:123
|
作者
Hunt, David [1 ]
Raivich, Gennadij [2 ]
Anderson, Patrick Norval [3 ]
机构
[1] Newham Univ Hosp, Med Educ Ctr, London, England
[2] UCL, Inst Womens Hlth, Perinatal Brain Repair Grp, London WC1E 6BT, England
[3] UCL, Res Dept Cell & Dev Biol, London WC1E 6BT, England
来源
关键词
ATF3; c-Jun; DORSAL-ROOT GANGLION; UNFOLDED PROTEIN RESPONSE; NEURONAL CELL-DEATH; CHRONIC CONSTRICTION INJURY; C-JUN PHOSPHORYLATION; STRESS-INDUCIBLE GENE; PERIPHERAL-NERVE; SPINAL-CORD; UP-REGULATION; AXONAL REGENERATION;
D O I
10.3389/fnmol.2012.00007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activating transcription factor 3 (ATF3) belongs to the ATE/cyclic AMP responsive element binding family of transcription factors and is often described as an adaptive response gene whose activity is usually regulated by stressful stimuli. Although expressed in a number of splice variants and generally recognized as a transcriptional repressor, ATF3 has the ability to interact with a number of other transcription factors including c-Jun to form complexes which not only repress, but can also activate various genes. ATF3 expression is modulated mainly at the transcriptional level and has markedly different effects in different types of cell. The levels of ATF3 mRNA and protein are normally very low in neurons and glia but their expression is rapidly upregulated in response to injury. ATF3 expression in neurons is closely linked to their survival and the regeneration of their axons following axotomy, and that in peripheral nerves correlates with the generation of a Schwann cell phenotype that is conducive to axonal regeneration. ATF3 is also induced by Toll-like receptor (TLR) ligands but acts as a negative regulator of TLR signaling, suppressing the innate immune response which is involved in immuno-surveillance and can enhance or reduce the survival of injured neurons and promote the regeneration of their axons.
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页数:17
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