Genetic Approaches to Investigate the Role of CREB in Neuronal Plasticity and Memory

被引:109
作者
Barco, Angel [1 ]
Marie, Helene [2 ]
机构
[1] Univ Miguel Hernandez, Consejo Super Invest Cient, Inst Neurociencias Alicante, Alicante 03550, Spain
[2] CNRS, UNSA, Inst Pharmacol Mol & Cellulaire, UMR6097, F-06560 Valbonne, France
关键词
CREB; Neuronal plasticity; Memory; Transgenic mice; Virus-mediated expression; ELEMENT-BINDING-PROTEIN; LONG-TERM-MEMORY; CAMP-RESPONSIVE ELEMENT; CONSTITUTIVELY ACTIVE FORM; VIRAL-MEDIATED EXPRESSION; FAMILY TRANSCRIPTION FACTORS; SYNAPTIC PLASTICITY; UP-REGULATION; MOLECULAR-MECHANISMS; TARGETED MUTATION;
D O I
10.1007/s12035-011-8209-x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In neurons, the convergence of multiple intracellular signaling cascades leading to cAMP-responsive element-binding protein (CREB) activation suggests that this transcription factor plays a critical role in integrating different inputs and mediating appropriate neuronal responses. The nature of this transcriptional response depends on both the type and strength of the stimulus and the cellular context. CREB-dependent gene expression has been involved in many different aspects of nervous system function, from embryonic development to neuronal survival, and synaptic, structural, and intrinsic plasticity. Here, we first review the different methodological approaches used to genetically manipulate CREB activity and levels in neurons in vivo in the adult brain, including recombinant viral vectors, mouse transgenesis, and gene-targeting techniques. We then discuss the impact of these approaches on our understanding of CREB's roles in neuronal plasticity and memory in rodents. Studies combining these genetic approaches with electrophysiology and behavior provide strong evidence that CREB is critically involved in the regulation of synaptic plasticity, intrinsic excitability, and long-term memory formation. These findings pave the way for the development of novel therapeutic strategies to treat memory disorders.
引用
收藏
页码:330 / 349
页数:20
相关论文
共 171 条
  • [1] A dominant-negative inhibitor of CREB reveals that it is a general mediator of stimulus-dependent transcription of c-fos
    Ahn, S
    Olive, M
    Aggarwal, S
    Krylov, D
    Ginty, DD
    Vinson, C
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) : 967 - 977
  • [2] Capture of the late phase of long-term Potentiation within and across the apical and basilar dendritic compartments of CA1 pyramidal neurons: Synaptic tagging is compartment restricted
    Alarcon, JM
    Barco, A
    Kandel, ER
    [J]. JOURNAL OF NEUROSCIENCE, 2006, 26 (01) : 256 - 264
  • [3] Regulated expression of VP16CREB in neuroblastoma cells: Analysis of differentiation and apoptosis
    Andreatta, CP
    Nahreini, P
    Hanson, AJ
    Prasad, KN
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 78 (04) : 570 - 579
  • [4] Balschun D, 2003, J NEUROSCI, V23, P6304
  • [5] Gene expression profiling of facilitated L-LTP in VP16-CREB mice reveals that BDNF is critical for the maintenance of LTP and its synaptic capture
    Barco, A
    Patterson, S
    Alarcon, JM
    Gromova, P
    Mata-Roig, M
    Morozov, A
    Kandell, ER
    [J]. NEURON, 2005, 48 (01) : 123 - 137
  • [6] Barco A, 2003, EXPERT OPIN THER TAR, V7, P101, DOI 10.1517/14728222.7.1.101
  • [7] Expression of constitutively active CREB protein facilitates the late phase of long-term potentiation by enhancing synaptic capture
    Barco, A
    Alarcon, JM
    Kandel, ER
    [J]. CELL, 2002, 108 (05) : 689 - 703
  • [8] BARCO A, 2007, REGULATION TRANSCRIP, P127
  • [9] Common molecular mechanisms in explicit and implicit memory
    Barco, Angel
    Bailey, Craig H.
    Kandel, Eric R.
    [J]. JOURNAL OF NEUROCHEMISTRY, 2006, 97 (06) : 1520 - 1533
  • [10] Retroviral vectors:: new applications for an old tool
    Barquinero, J
    Eixarch, H
    Pérez-Melgosa, M
    [J]. GENE THERAPY, 2004, 11 (Suppl 1) : S3 - S9