Targeting CREB signalling in neurogenesis

被引:104
作者
Dworkin, Sebastian [2 ]
Mantamadiotis, Theo [1 ]
机构
[1] Univ Patras, Dept Med, Patras 26500, Greece
[2] Bone Marrow Res Labs, Parkville, Vic 3050, Australia
关键词
cancer; CREB; neural stem cells; neurogenesis; transcription; ELEMENT-BINDING PROTEIN; LONG-TERM-MEMORY; AMP-RESPONSE ELEMENT; ADULT HIPPOCAMPAL NEUROGENESIS; FAMILY TRANSCRIPTION FACTORS; DENTATE GYRUS; GENE-EXPRESSION; PROGENITOR PROLIFERATION; NEWBORN NEURONS; CYCLIN D2;
D O I
10.1517/14728222.2010.501332
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Importance of the field: Expansion and ultimately homeostasis of neural cell number is exquisitely regulated by molecular genetic networks operating in neural stem and progenitor cells (NSPCs) and in the neural stem cell niche during embryogenesis and in the adult brain. Transcription factors are crucial in orchestrating the correct cell-specific and temporal expression of all factors involved in these signalling networks. Aberrant expression of these factors can lead to abnormal brain development if this occurs during embryogenesis. In the adult brain, loss of neurogenic potential can lead to cognitive deficits and in combination with neural death can even contribute to neurodegenerative disease progress. Areas covered in this review: This review focuses on a number of recent discoveries identifying the role of the transcription factor cAMP response element binding (CREB) protein in regulating brain development and neurogenesis in the adult brain. What the reader will gain: The significance of these discoveries is presented in the context of human brain disorders and how this knowledge could contribute to pharmacotherapeutic interventions targeting CREB signalling aimed at treating such diseases. Take home message: Unravelling these precise molecular genetic networks is crucial to understanding how neural stem and progenitor cells function
引用
收藏
页码:869 / 879
页数:11
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