Regulation of hippocampal synaptic plasticity by cyclic AMP-dependent protein kinases

被引:256
作者
Nguyen, PV [1 ]
Woo, NH
机构
[1] Univ Alberta, Sch Med, Ctr Neurosci, Dept Physiol, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Sch Med, Ctr Neurosci, Dept Psychiat, Edmonton, AB T6G 2H7, Canada
关键词
D O I
10.1016/j.pneurobio.2003.12.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Protein kinases critically regulate synaptic plasticity in the mammalian hippocampus. Cyclic-AMP dependent protein kinase (PKA) is a serine-threonine kinase that has been strongly implicated in the expression of specific forms of long-term potentiation (LTP), long-term depression (LTD), and hippocampal long-term memory. We review the roles of PKA in activity-dependent forms of hippocampal synaptic plasticity by highlighting particular themes that have emerged in ongoing research. These include the participation of distinct isoforms of PKA in specific types of synaptic plasticity, modification of the PKA-dependence of UP by multiple factors such as distinct patterns of imposed activity, environmental enrichment, and genetic manipulation of signalling molecules, and presynaptic versus postsynaptic mechanisms for PKA-dependent LTP. We also discuss many of the substrates that have been implicated as targets for PKA's actions in hippocampal synaptic plasticity, including CREB, protein phosphatases, and glutamatergic receptors. Future prospects for shedding light on the roles of PKA are also described from the perspective of specific aspects of synaptic physiology and brain function that are ripe for investigation using incisive genetic, cell biological, and electrophysiological approaches. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:401 / 437
页数:37
相关论文
共 489 条
[41]   A quantitative autoradiographic study of [3H]cAMP binding to cytosolic and particulate protein kinase A in post-mortem brain staged for Alzheimer's disease neurofibrillary changes and amyloid deposits [J].
Bonkale, WL ;
Cowburn, RF ;
Ohm, TG ;
Bogdanovic, N ;
Fastbom, J .
BRAIN RESEARCH, 1999, 818 (02) :383-396
[42]   DEFICIENT LONG-TERM-MEMORY IN MICE WITH A TARGETED MUTATION OF THE CAMP-RESPONSIVE ELEMENT-BINDING PROTEIN [J].
BOURTCHULADZE, R ;
FRENGUELLI, B ;
BLENDY, J ;
CIOFFI, D ;
SCHUTZ, G ;
SILVA, AJ .
CELL, 1994, 79 (01) :59-68
[43]   Increasing numbers of synaptic puncta during late-phase LTP: N-cadherin is synthesized, recruited to synaptic sites, and required for potentiation [J].
Bozdagi, O ;
Shan, W ;
Tanaka, H ;
Benson, DL ;
Huntley, GW .
NEURON, 2000, 28 (01) :245-259
[44]  
BRADLEY A, 1993, RECENT PROG HORM RES, V48, P237
[45]  
Bradley J, 1997, J NEUROSCI, V17, P1993
[46]   PKA isoforms, neural pathways, and behaviour: making the connection [J].
Brandon, EP ;
Idzerda, RL ;
McKnight, GS .
CURRENT OPINION IN NEUROBIOLOGY, 1997, 7 (03) :397-403
[47]   HIPPOCAMPAL LONG-TERM DEPRESSION AND DEPOTENTIATION ARE DEFECTIVE IN MICE CARRYING A TARGETED DISRUPTION OF THE GENE ENCODING THE RI-BETA SUBUNIT OF CAMP-DEPENDENT PROTEIN-KINASE [J].
BRANDON, EP ;
ZHUO, M ;
HUANG, YY ;
QI, M ;
GERHOLD, KA ;
BURTON, KA ;
KANDEL, ER ;
MCKNIGHT, GS ;
IDZERDA, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (19) :8851-8855
[48]  
BREGMAN DB, 1989, J BIOL CHEM, V264, P4648
[49]   Retrograde amnesia for spatial memory induced by NMDA receptor-mediated long-term potentiation [J].
Brun, VH ;
Ytterbo, K ;
Morris, RGM ;
Moser, MB ;
Moser, EI .
JOURNAL OF NEUROSCIENCE, 2001, 21 (01) :356-362
[50]   Designing isoform-specific peptide disruptors of protein kinase A localization [J].
Burns-Hamuro, LL ;
Ma, YL ;
Kammerer, S ;
Reineke, U ;
Self, C ;
Cook, C ;
Olson, GL ;
Cantor, CR ;
Braun, A ;
Taylor, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :4072-4077