Structural Components of Synaptic Plasticity and Memory Consolidation

被引:310
作者
Bailey, Craig H. [1 ,2 ,3 ]
Kandel, Eric R. [1 ,2 ,3 ,4 ]
Harris, Kristen M. [5 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Neurosci, New York, NY 10027 USA
[2] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[3] Kavli Inst Brain Sci, New York, NY 10032 USA
[4] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[5] Univ Texas Austin, Dept Neurosci, Inst Neurosci, Ctr Learning & Memory, Austin, TX 78712 USA
关键词
LONG-TERM POTENTIATION; CELL-ADHESION MOLECULE; LOCAL PROTEIN-SYNTHESIS; SPONTANEOUS TRANSMITTER RELEASE; AMPA RECEPTOR TRAFFICKING; PRESYNAPTIC ACTIVE ZONES; GILL-WITHDRAWAL REFLEX; DENDRITIC SPINES; DENTATE GYRUS; N-CADHERIN;
D O I
10.1101/cshperspect.a021758
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Consolidation of implicit memory in the invertebrate Aplysia and explicit memory in the mammalian hippocampus are associated with remodeling and growth of preexisting synapses and the formation of new synapses. Here, we compare and contrast structural components of the synaptic plasticity that underlies these two distinct forms of memory. In both cases, the structural changes involve time-dependent processes. Thus, some modifications are transient and may contribute to early formative stages of long-term memory, whereas others are more stable, longer lasting, and likely to confer persistence to memory storage. In addition, we explore the possibility that trans-synaptic signaling mechanisms governing de novo synapse formation during development can be reused in the adult for the purposes of structural synaptic plasticity and memory storage. Finally, we discuss how these mechanisms set in motion structural rearrangements that prepare a synapse to strengthen the same memory and, perhaps, to allow it to take part in other memories as a basis for understanding how their anatomical representation results in the enhanced expression and storage of memories in the brain.
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页数:29
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共 297 条
[1]
Abraham WC, 1997, HIPPOCAMPUS, V7, P137, DOI 10.1002/(SICI)1098-1063(1997)7:2<137::AID-HIPO3>3.0.CO
[2]
2-K
[3]
Abraham WC, 2002, J NEUROSCI, V22, P9626
[4]
Heterosynaptic metaplasticity in the hippocampus in vivo:: A BCM-like modifiable threshold for LTP [J].
Abraham, WC ;
Mason-Parker, SE ;
Bear, MF ;
Webb, S ;
Tate, WP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10924-10929
[5]
Metaplasticity: A new vista across the field of synaptic plasticity [J].
Abraham, WC ;
Tate, WP .
PROGRESS IN NEUROBIOLOGY, 1997, 52 (04) :303-323
[6]
Metaplasticity: The plasticity of synaptic plasticity [J].
Abraham, WC ;
Bear, MF .
TRENDS IN NEUROSCIENCES, 1996, 19 (04) :126-130
[7]
Knowing a nascent synapse when you see it [J].
Ahmari, SE ;
Smith, SJ .
NEURON, 2002, 34 (03) :333-336
[8]
Assembly of presynaptic active zones from cytoplasmic transport packets [J].
Ahmari, SE ;
Buchanan, J ;
Smith, SJ .
NATURE NEUROSCIENCE, 2000, 3 (05) :445-451
[9]
Cell-cell interactions in synaptogenesis [J].
Akins, MR ;
Biederer, T .
CURRENT OPINION IN NEUROBIOLOGY, 2006, 16 (01) :83-89
[10]
C/EBP IS AN IMMEDIATE-EARLY GENE REQUIRED FOR THE CONSOLIDATION OF LONG-TERM FACILITATION IN APLYSIA [J].
ALBERINI, CM ;
GHIRARDI, M ;
METZ, R ;
KANDEL, ER .
CELL, 1994, 76 (06) :1099-1114